Journal Logo


Increasing physical activity: a quantitative synthesis


Author Information
Medicine & Science in Sports & Exercise: June 1996 - Volume 28 - Issue 6 - p 706-719
  • Free


Sedentariness is a burden to the public's health in the United States, accounting for an estimated 200,000 deaths annually(45) from coronary heart disease(5,21,31), colon cancer(57), and non-insulin-dependent diabetes(26,30,35). Naturally occurring increases in leisure physical activity (42) or cardiorespiratory fitness (6) are associated with decreased mortality from coronary heart disease and all-causes, whereas regular physical activity is an effective adjuvant for the primary or secondary treatment of hypertension(2,21), obesity(44,58), osteoporosis(20,46), and major depression(17). Moreover, sedentary leisure is highly prevalent(14). Despite national health policy that physical activity be increased (59), best estimates indicate no change in secular physical activity patterns during the past decade(12). Depending upon definition, 25%-60% of U.S. adults are sedentary (12,14,59), just 10%-20% are active enough to increase or maintain physical fitness, while the rest are active sporadically (12,14), with uncertain benefits for health.

The status of physical inactivity in the U.S. is explainable in large part by a limited understanding of interventions available for increasing physical activity. This is true especially in community and clinical medicine, where primary-care physicians and other health care providers have unique opportunities to influence healthful changes in physical activity habits. Although the medical office has priority for implementing physical activity interventions (59), physicians typically report they spend little time counseling patients about exercise(32,36), lacking confidence about their training and abilities to change exercise habits(34,40,55,60,61) even when endorsing the salutary benefits of leisure physical activity for their patients (37,62). Furthermore, the partnership between clinical medicine, which focuses on a patient, and community medicine, which encompasses a population, is poorly defined for guiding interventions to increase physical activity (8,24).

Our purpose for the analysis reported herein is to provide a quantitative synthesis of the literature examining the effects of interventions used to increase physical activity. Our goals are to describe the efficacy of such interventions and the factors that moderate their success in order to guide public health policy, form hypotheses testable by further experimentation, and inform physicians and other health care providers about interventions that increase physical activity in communities and patients.


One-hundred twenty-seven published studies and 14 dissertations were located from 1965 through August, 1995, by computer searches of literature in the English language using Medline, Current Contents, Psychinfo, SOCIAL SCISEARCH, ERIC, and Dissertation Abstracts International data bases, bibliographic searches, and a personal retrieval system, cross-referenced with expert colleagues. Index words were behavior modification, health promotion, health education adherence, compliance, physical activity, fitness, and exercise. Five redundant publications were excluded. A quantitative synthesis then was conducted using standard meta-analytic procedures(23,25,27,49) with the aid of two statistical software programs: Meta 5.3 (56) and SPSS/PC- 6.0 (39).

Criteria for including a study were: 1) The dependent variable was a measure of physical activity consistent with consensus definitions used in public health (13,43) or a measure of physical fitness that is a surrogate of physical activity (1). 2) The independent variable was an intervention designed to increase habitual physical activity. 3) Outcomes of the intervention were quantified and could be compared with a variance estimate of the outcome from a control group or condition in the absence of the intervention. 4) An effect size could be expressed as a Pearson correlation coefficient r(50), permitting effects to be calculated from studies that used diverse statistical presentations including frequencies, percentages, graphs, t-tests, and chi-square- and F-tests with a single df, when means and standard deviations were not reported(49,50). Sixty located studies were excluded. Commonly used statistical guideposts for evaluating the size of r as a small, moderate, or large effect are 0.10, 0.30, or 0.50(15,50).

The use of r also permitted a binomial effect size display(51) of the interventions' effects, interpreted as a practical measure of the success of an intervention. An r equaling 0.00 equates to a binomial effect of zero, reflecting a 50% chance for success in the absence of intervention. This approximates the mean success rate of nearly 50% reported for adherence to supervised (19,22) or community-based (54) exercise programs in the absence of intervention. An r of 0.20 is equivalent to an increase in success from 50% to 60%, whereas an r of 0.40 indicates an increase to 70%. When possible, effect sizes were calculated by subtracting the mean change for a control group or condition from the mean change for an experimental group or condition, and dividing this difference by the initial standard deviation of the control scores (15,23). This procedure reduced bias from pooling experimental variance and from the correlated variance of repeated measures (4). For multiple-baseline studies, intervention effects were compared to the initial baseline using the mean of each subject's effects. Interrater agreement for r was determined by intraclass correlation (RI) computed from ANOVA of r judged by four pairs of raters. Each rater pair blindly retrieved effects from 10 to 15 articles selected separately from among the 127 articles. RI ranged from 0.89 to 0.96. We also examined variation in effects according to moderating variables deemed practically important for understanding and optimizing effective interventions. Definitions of the moderators are provided in Table 1.

We retrieved 445 effects from the 127 studies based on ≈131,156 people. Fisher's z transformation of r (zr) was used for analyses to adjust for the nonnormal distribution of r, protecting against small sampling bias in estimates of the population r. The reported values of r are back transformations from z. Factors relevant for community and clinical medicine that might moderate the estimated population effect of the interventions were considered by comparing effects among features describing subjects, interventions, settings, and physical activity. Most studies reported multiple effects owing to separate effects derived according to age, race, or gender, concurrent estimates of physical activity using different measures, or follow-up measures of physical activity after an intervention ended. The mean effect was used when a study reported multiple measures of physical activity using the same method (e.g., multiple self-reports). The number of effects and the mean effect size per study were unrelated (r (125) = -0.07, P = 0.45), but we adopted a conservative statistical criterion (P < 0.001) to protect against Type I error when using several effects per study in analyses of moderators (49,53). Small sample sizes can increase Type II error (25). Hence, individual effects also were weighted by sample size (25,27) to adjust for sampling errors in r, giving more credence to studies with large samples.


A stem-and-leaf display of the 445 effects is presented inFigure 1, indicating a nearly normal distribution of effects, with a negative skewness. The mean value of r was 0.34 (95% CI, 0.26-0.42), or 0.75 (95% CI, 0.70-0.79) after weighting by sample size. The effect r = 0.34 approximates an effect of three-fourths standard deviation(50). The effects were heterogeneous(49,56). A correlation of 0.25 between sample size and zr contributed to the larger weighted estimate of r. The corresponding binomial effect represents a potential increase in success rates after intervention from 50% to 67%, or to 88% for the weighted analysis. The estimated population value of r was 0.64, or 0.76 for the weighted analysis, after adjustment (25,27) for a reliability of r = 0.80 among the measures of physical activity (1).

In contrast to results from the published sources, 14 unpublished doctoral dissertations reporting 55 effects for 668 subjects yielded a mean r of 0.17(95% CI, -0.10 to 0.41), or 0.09 (95% CI, -0.18 to 0.35) when effects were weighted by sample size. Hence, we estimated the impact of unpublished null findings upon the population value of r derived from the published studies using the fail-safe N(41); a reduction of r to 0.20 from the observed values of 0.34 and 0.75 requires 317 and 1219 null findings, respectively.

Focused contrasts (49,52), each tested as Z atP < 0.001, subsequently were conducted to determine if moderators describing subjects, settings, or features of interventions and physical activity important for understanding and implementing interventions in community and clinical medicine might account for variability in the mean effect size. Effects for each moderator are presented inTable 2 as mean r with a 95% confidence interval. Variables that were significant moderators also were entered into a linear multiple regression model to clarify their independent effects for explaining variation in zr. Moderators with more than two nonordinal levels were dichotomized based on results from the contrasts.

Moderating Variables Weighted by Sample Size

Subject attributes. Effect sizes did not differ between males and females, between age groups, or between whites and non-whites, but studies that reported on samples combining race or ages reported effects that were larger than those for specific race or age groups. The effect among healthy subjects was larger contrasted with all groups of patients. Small effects were observed in studies of people who had CHD, high risk for CHD, or other chronic diseases or physically or developmentally disabling conditions, but there were relatively few studies of interventions with patients.

Intervention type and setting. Effect sizes differed by intervention type, whereby behavior modification approaches were associated with effects that were larger compared with the other approaches. There were differences according to the manner of delivery of the intervention; effects were larger among studies using mediated approaches contrasted with face-to-face delivery. Interventions in community settings and interventions delivered to groups reported larger effects, contrasted with those in schools and other settings or with delivery to individuals, the family, and to an individual combined within a group, respectively. Effects were larger when the physical activity was not supervised compared with a supervised physical activity program. Effects were unrelated to the number of weeks the intervention, r (443) = -0.07, or the follow-up period, r (171) = -0.06,P > 0.05, lasted.

Physical activity features. Effect sizes differed according to the mode of physical activity. Effects for active leisure time were larger contrasted with exercise programs prescribing strength, aerobic exercise, or aerobic exercise combined with other fitness activities. Effect sizes did not differ according to the weekly frequency or daily duration, but studies that observed physical activities carried out at a low intensity reported larger effects compared with studies using estimates of physical activities conducted at higher intensities. Effects from studies using an objective measure of attendance or direct observation were larger compared with those using self-reports by participants or surrogate measures of physical activity based on changes in physiological responses to exercise testing or strength. Only about 25% of the studies reported follow-up measures of physical activity to determine if increases in physical activity were maintained after the intervention ended, but followup effects generally were small.

Multiple regression analysis. Direct entry of the significant moderating variables into a multiple linear regression analysis indicated that 9 variables independently accounted for variation in zr: age, physical activity mode, intervention delivery, health status, physical activity measure, physical activity intensity, social context, intervention type, and research design, P < 0.05. Reentry of these variables into the regression model yielded a multiple R of 0.66, adjusted R2 = 0.42,F (9,435) = 36.9, P < 0.0001. Research design did not add to the final model. Results are presented in Table 3.

Weighting versus Not Weighting by Sample Size?

Weighting by sample size yields a better estimate of the true effect of interventions in the population, which is especially important when hypotheses or policy judgments are formed about interventions to increase physical activity in a community. Nonetheless, sampling bias in the relationship between zr and sample size can create anomalies confounding the interpretation of moderators. Examples presently are the larger effects for samples comprised of several age categories or more than one race in the weighted analysis, contrasted with the small effects for studies that reported separate effects for specific age groups or for whites and non-whites. Numerous studies intervening with large samples did not report analyses separately based on age or race, focusing on mediated approaches with community-based groups participating in unsupervised physical activity of low intensity.

Hence, weighting zr by sample size can obscure important effects observed in studies of smaller groups of people that may prove to be good estimates of population effects upon further sampling. This concern particularly applies when comparing the effects among interventions applied in clinical health care settings where the mean sample was about 50 people, contrasted with community-based interventions where the mean sample was about 925 people. Several of the aforementioned moderators are important features of clinical applications of physical activity. Thus, additional contrasts were focused on the moderator variables using zr without weighting by sample size.

Moderating Variables Not Weighted by Sample Size

Subject attributes. In contrast with the weighted analysis, effects from samples of more than one race did not differ from the effects for specific races. Also, effects from studies sampling patients who were obese or who had developmental or physical disabilities and a chronic illness other than cardiovascular disease were larger than effects of studies of healthy people, all of which were larger than effects from studies of people with, or at risk for, cardiovascular disease.

Intervention type and setting. Behavior modification again had larger effects contrasted with the other interventions. In contrast to the weighted analysis, effects did not differ according to social context, the method of delivering the interventions, or according to the intensity of the physical activity, or whether the physical activity was supervised or free-living without supervision. Also, in contrast to the weighted analysis, effects of interventions conducted in community settings were similar to those applied in home, school, worksite, and health care settings. Effects were related inversely to the number of weeks in the intervention, r (443) = -0.20,P < 0.001 and the follow-up, r (171) = -0.18, P < 0.01, periods.

Physical activity features. In contrast with the weighted analysis, effects did not differ according to mode or intensity of physical activity. As was the case for the weighted analysis, effects at follow-up generally were small.

Multiple regression analysis. Direct entry of the significant moderating variables into a multiple linear regression analysis indicated that intervention type, intervention length, and research design accounted for variation in zr, P < 0.05. The regression model yielded a multiple R of 0.48, adjusted R2 = 0.23, F (3,441) = 44.4,P < 0.0001. Health status did not contribute to the model. Results are presented in Table 4.

Research Design

Effects derived from a pre- or quasi-experimental design(11) (N = 169) were larger (mean ± 95% CI (0.87 ± 0.82-0.90 and 0.53 ± 0.41-0.64) than those from randomized experiments (N = 276) (0.10 ± 0.00-0.21 and 0.21± 0.09-0.32) in the weighted and unweighted analyses, respectively,P < 0.001. Though research design did not independently influence effect size in the weighted analysis, we further examined the impact of lowered internal validity on the moderator analyses by adjusting zr for the quality of the research design using fractional weights(49) for effects from studies employing a pre- or quasi-experimental design. Contrasts within the moderators then were repeated. The quality of the research design generally did not interact with the moderator variables. Exceptions were that, without weighting by sample size, the studies using pre- or quasi-experimental designs yielded larger effects for low-intensity physical activity and for health care settings, contrasted with the studies using experimental designs, whereas research design in the weighted analysis did not moderate the pattern of effects for physical activity intensity or the intervention setting. Interventions in health care settings, contrasted with those in a community, typically used pre- or quasi-experimental designs, studying supervised physical activity after shorter intervention periods. Otherwise, clinical and community interventions did not differ in the gender, age, or race of subjects or in the features of the interventions and physical activity studied. Hence, the differences in the impact of moderators observed for the weighted vs unweighted analyses were not biased by differing distributions of the moderating variables, but can be partly attributed to the manner by which community versus clinical intervention studies were conducted or reported.


A conservative interpretation of our quantitative synthesis of the literature, gauged by statistical guideposts (15), is that interventions for increasing physical activity have a moderately large effect. The effect also is large practically, equivalent to improving success from the typical rate of 50% without intervention to about 70%-88%(51). Though summaries from a meta-analysis require experimental confirmation, our aforementioned results suggest directions about the best ways to implement effective interventions for increasing physical activity in community and clinical medicine. The analysis of effects weighted by sample size suggests that interventions based on the principles of behavior modification, delivered to healthy people in a community, are associated with large effects, particularly when the interventions are delivered to groups using mediated approaches or when the physical activity is unsupervised, emphasizing leisure physical activity of low intensity, regardless of the duration or frequency of participation. The multiple linear regression model of the moderating variables supported that the larger effects reported for combined ages, behavior modification, and the delivery of the interventions using media, to groups or to healthy subjects, describing low-intensity, active leisure physical activity measured by observation, were independent of each other; whereas the influences on effect size by community setting, combined races, and a pre- or quasi-experimental research design found in the univariate analysis by contrasts were not independent of the other moderating variables.

Since the mean effect for each level of the significant moderating variables was heterogeneous (49,56), interactions among the moderators or their levels will better explain the findings suggested by our independent analysis of moderators. Not all studies reported information on each of the moderators we examined. Hence, there were not enough studies and effects to permit a statistically powerful analysis of interactions among the moderators, a limitation to inferring causality by moderators that is common among meta-analyses.

Our quantitative analysis provides some support for consensus opinions(8,18,28) that modifying traditional guidelines for exercise programming (3) to accommodate moderately intense physical activities of varied types(8,18) in a community using mediated(28), as well as face-to-face, approaches will increase participation among segments of the sedentary population(43). The maintenance of successful physical activity after the conclusion of an intervention has been less encouraging, implying a need for sustained or repeated implementation of interventions. Though past studies have reported little success in increasing physical activity among people representing racial or ethnic minorities or older ages, these groups have been underrepresented in past studies and should receive more attention by researchers in the future.

The aforementioned findings imply an influential role by community medicine for increasing physical activity. Nonetheless, clinical uses of physical activity applied toward the secondary prevention of health problems also are important for public health. When the size of the studies' samples was ignored, interventions in health care settings and schools were similarly effective compared with intervention in the community, regardless of the features of the physical activity. Sample size ignored, interventions were most effective when they employed behavior modification approaches, often combining reinforcement- and stimulus-control. In addition to behavior modification, interventions that altered the physical education curriculum in schools or combined two or more types of interventions were effective. Also, interventions targeting patient groups, other than those with cardiovascular disease or high risk, were more effective compared with interventions targeting apparently healthy people. Though the effects of setting or health status were not independent influences on intervention effectiveness, they warrant experimental testing.

The absence of effects by interventions using health education or health risk appraisals is consistent with a narrative review of the literature(16). In contrast, the apparent ineffectiveness of cognitive-behavior modification and the supervised prescription of moderate exercise is not consistent with previous narrative reviews(18,28). The large confidence intervals surrounding the mean effect, usually including zero, for interventions other than behavior modification, coupled with the smaller number of effects, makes it premature to conclude that interventions other than behavior modification are ineffective for increasing physical activity. This caveat also applies to interventions with heart patients for whom few effects were reported. Also, it appears that interventions other than behavior modification have been implemented in widely varying ways, especially in the case of cognitive-behavior modification. Cognitive-behavior modification techniques often were combined with other interventions, precluding a determination of their independent effects in many studies. These combination interventions had the same effect size as interventions using cognitive-behavior modification, alone. Moreover, most studies using cognitive-behavior modification did not base the interventions on a broader theoretical model of behavior change(29,47).

When weighted by sample size, the effect for pre- and quasi-experimental studies was markedly larger compared with randomized experimental studies, including those using a minimally effective intervention condition (i.e., a placebo). However, a randomized research design is extremely difficult and costly to implement in community- or population-based studies. The use of a placebo for control comparisons was rare, and usually it is not feasible for a population-based study. Scientific quality notwithstanding, whether the research design was experimental versus pre- or quasi-experimental was not an independent influence on the size of effects when weighted by sample size and, ignoring sample size, had little impact on the pattern of moderating effects other than in health care settings, where effects were larger for pre- or quasi-experimental designs. Nonetheless, it is important to not infer prematurely that a moderator implied by our meta-analysis is a casual determinant of variations in effects when the studies we reviewed did not experimentally manipulate levels of the moderator.

Few studies verified self-reported physical activity by measuring increases in fitness expected to result from increased physical activity or by concomitantly using an objective measure of activity such as a motion sensor or observation. While increases in physical activity typically were largest when an objective measure of attendance or observation was used, the failure of interventions to increase physical activity when it was estimated by a surrogate measure of physical fitness indicates that the validity of physical activity measures other than observation remains an important methodology dilemma for the study of physical activity in public health. Furthermore, it is important to determine whether the absolute levels of increased activity were adequate to increase physical fitness (3) or decrease the risk for disease morbidity or all-cause mortality(6,31,42). Only about one-fourth of the studies reviewed herein reported a follow-up to the intervention, but those studies typically showed that increases in physical activity or fitness associated with the interventions were diminished as time passed after the intervention ended. Many of the community studies that reported large effects did not report on the maintenance of physical activity after the intervention's conclusion, or reported a return near to the pre-intervention activity level within a few weeks after the intervention.

Two implications of our literature analysis especially are important for understanding the roles of community and clinical medicine in promoting physical activity. One arises from the larger effects by interventions using media, or applied in large groups, contrasted with smaller effects by interventions to small groups or in a clinical setting, or using face-to-face delivery. Though the larger effects reported in community settings were not independent of the other moderators, the pattern of moderator influences suggested influential roles by public health initiatives and community-based medicine for increasing physical activity. Until around 1990, most intervention studies used single dimensional approaches with small numbers of people of similar gender, race, ethnicity, education, and economic and health status (16,18). More recently, community-based interventions applying psychological and behavioral theories for behavior change have predominated (18,28). These approaches extend beyond the traditional practice of face-to-face counseling to include changes in organizational (community recreation centers, churches, diffusion strategies through schools), environmental (e.g., facility planning), and social (e.g., family interventions) factors or they use cost-effective or convenient vehicles (e.g., mailings, telecommunication) for reaching many people who are not accessible or amenable to traditional interventions based in clinical settings. Such interventions are appropriately part of community medicine, but they do not depend upon a direct physician-patient encounter. They warrant further experimental testing for effectiveness.

Another implication of our analysis is that previous interventions for increasing physical activity applied in health care settings, including cognitive-behavior modification, were not implemented optimally. Our qualitative evaluation of the studies suggests this may be explainable because the studies did not use standardized approaches based on newer theories about how health behavior, specifically physical activity, changes. Recently, a successful clinical trial (10) based in the physician's office used a theoretical model grounded in cognitive-behavior modification(47) that triages patients into stages of readiness for changing their physical activity habits, then introducing standardized counseling by the physician, supported by nurses and staff, that is stage-appropriate. Such an approach offers more promise for increasing physical activity than the counseling approaches traditionally used by physicians (33,36,61) and deserves evaluation by clinically research. About 80% of the U.S. population has annual contact with a physician, with 65% of patient contacts involving primary-care specialities (38). Nearly 50% of practicing physicians in the U.S., about 245,000 physicians, are in primary-care specialities of family or general practice, internal medicine, pediatrics, and obstetrics-gynecology (48) which permit physical activity intervention during patient counseling. Similarly, there are approximately 250,000 nurses in primary care (9) who can support physical activity interventions applied in the medical office. Hence, exploiting more fully the impact of the physician-patient encounter remains an important area for experimental tests of effective interventions for increasing the nation's level of physical activity.

The relative contributions by community and clinical medicine to successful interventions for increasing physical activity warrant accelerated testing by clinical trials. This is important particularly among people with high risk for cardiovascular disease, whereby physical activity exerts its greatest influence in reducing premature death (6,42), yet few interventions for increasing physical activity have been conducted with success in that group. An emphasis also is needed for understanding the ways by which cognitive-behavior modification can be uniformly applied to increase physical activity, since it is theoretically superior to health education, health risk appraisal, and exercise prescription which, though easily implemented, have not proved effective for increasing physical activity.

Controlled experiments are required to confirm the varying effects of interventions suggested by the foregoing analysis and how intervention components, settings, and population segments can be combined to optimally increase and maintain physical activity in the largely sedentary U.S. population. Nonetheless, our quantitative synthesis of the literature demonstrates that the use of behavior modification has efficacy for increasing physical activity, providing a basis for optimism among professionals in public health and medicine that physical activity can be increased.

Figure 1-Stem-and-leaf-display for 445 effect sizes (r).
Figure 1-Stem-and-leaf-display for 445 effect sizes (r).


1. Ainsworth, B. E., H. J. Montoye, and A. S. Leon. Methods of assessing physical activity during leisure and work. In: Physical Activity, Fitness, and Health: International Proceedings and Consensus Statement, C. Bouchard, R. Shephard, and T. Stephens (Eds.). Champaign, IL: Human Kinetics, 1994, pp. 146-159.
2. American College Of Sports Medicine. Physical activity, physical fitness, and hypertension. Med. Sci. Sports Exerc. 25:i-x, 1993.
3. American College Of Sports Medicine. Position statement on the recommended quality and quantity of exercise for developing and maintaining fitness in healthy adults. Med. Sci. Sports Exerc. 22:265-274, 1990.
4. Becker, B. J. Synthesizing standardized mean-change measures. Br. J. Math. Stat. Psychol. 41:257-278, 1988.
5. Berlin, J. A. and G. A. Colditz. A meta-analysis of physical activity in the prevention of coronary heart disease. Am. J. Epidemiol. 132:612-628, 1990.
6. Blair, S. N., H. W. Kohl III, C. E. Barlow, R. S. Paffenbarger, L. W. Gibbons, and C. A. Macera. Changes in physical fitness and all-cause mortality. A prospective study of healthy and unhealthy men.J.A.M.A. 273:1093-1098, 1995.
7. Blair, S. N., H. W. Kohl III, R. S. Paffenbarger, Jr., D. G. Clark, K. H. Cooper, and L. W. Gibbons. Physical fitness and all-cause mortality: a prospective study of healthy men and women. J.A.M.A. 262:2395-2401, 1989.
8. Blair, S. N., K. E. Powell, T. L. Bazzarre, et al. Physical inactivity. Workshop V. AHA Prevention Conference III. Behavior Change and Compliance: Keys to improving cardiovascular health.Circulation 88:1402-1405, 1993.
9. Bureau Of Health Professions. Factbook: Health Personnel, U.S. HRSA-P-AM-93-1, 1993, pp. 1-76.
10. Calfas, K. J., B. J. Long, J. F. Sallis, W. J. Wooten, M. Pratt, and K. Patrick. A controlled trial of physician counseling to promote the adoption of physical activity. Prev. Med. (in press).
11. Campbell, D. T. and J. C. Stanley. Experimental and Quasi-Experimental Designs for Research. Chicago: Rand McNally & Company, 1966, pp. 1-84.
12. Caspersen, C. J., R. K. Merritt, and T. Stephens. International physical activity patterns: a methodological perspective. In:Advances in Exercise Adherence, R.K. Dishman (Ed.). Champaign, IL: Human Kinetics, 1994, pp. 73-110.
13. Caspersen, C. J., K. E. Powell, and G. M. Christenson. Physical activity, exercise, and physical fitness: definitions and distinctions for health-related research. Public Health Rep. 100:126-130, 1985.
14. Centers For Disease Control And Prevention. Behavioral risk factor surveillance, 1986-1990. MMWR 1991;40(SS-4):1-23.
15. Cohen, J. Statistical Power Analysis for the Behavioral Sciences, 2nd Ed. New York: Academic Press, 1988, pp. 1-567.
16. Dishman, R. K. Increasing and maintaining exercise and physical activity. Behav. Ther. 22:345-378, 1991.
17. Dishman, R. K. Medical psychology in exercise and sport. Med. Clin. North Am. 69:123-143, 1985.
18. Dishman, R. K. and J. F. Sallis. Determinants and interventions for physical activity and exercise. In: Physical Activity, Fitness, and Health: International Proceedings and Consensus Statement, C. Bouchard, R. J. Shephard, and T. Stephens (Eds.). Champaign, IL: Human Kinetics Publishers, 1994, pp. 214-238.
19. Dishman, R. K., J. F. Sallis, and D. Orenstein. The determinants of physical activity and exercise. Public Health Rep. 100:158-171, 1985.
20. Drinkwater, B. L. Physical activity, fitness, and osteoporosis. In: Physical Activity, Fitness, and Health: International Proceedings and Consensus Statement, C. Bouchard, R. J. Shephard, and T. Stephens (Eds.). Champaign, IL: Human Kinetics Publishers, 1994, pp. 724-736.
21. Fletcher, G. F., S. N. Blair, J. Blumenthal, et al. Statement on exercise: benefits and recommendations for physical activity programs for all Americans. Circulation 86:2726-2730, 1992.
22. Franklin, B. A. Program factors that influence exercise adherence. In: Exercise Adherence: Its Impact on Public Health, R. K. Dishman (Ed.). Champaign, IL: Human Kinetics, 1988, pp. 237-258.
23. Glass, G. V., B. McGraw, and M. L. Smith.Meta-analysis In Social Research. London: Sage Publications, 1981, pp. 1-279.
24. Harris, S. S., C. J. Caspersen, G. H. Defries, and E. H. Estes. Physical activity counseling for health adults as a primary preventive intervention in the clinical setting. J.A.M.A. 264:2654-2659, 1989.
25. Hedges, L. V. and I. Olkin. Statistical Methods for Meta-analysis. San Diego: Academic Press, 1985, pp. 1-369.
26. Helmrich, S. P., D. R. Ragland, R. W. Leung, and R. S. Paffenbarger, Jr. Physical activity and reduced occurrence of non-insulin-dependent diabetes mellitus. N. Engl. J. Med. 325:147-152, 1991.
27. Hunter, J. E. and F. L. Schmidt. Methods of Meta-analysis: Correcting Error and Bias in Research Findings. Newbury Park, CA: Sage Publishers, 1990.
28. King, A. C., S. N. Blair, D. Bild et al. Determinants of physical activity and interventions in adults. Med. Sci. Sports Exerc. (Suppl. 24):S221-S236, 1992.
29. Knapp, D. N. Behavioral management techniques and exercise promotion. In: Exercise Adherence: Its Impact on Public Health, R. K. Dishman (Ed.). Champaign, IL: Human Kinetics, 1988, pp. 203-236.
30. Kriska, A. M., S. N. Blair, and M. A. Pereira. The potential role of physical activity in the prevention of non-insulin-dependent diabetes mellitus. Exerc. Sport Sci. Rev. 22:121-143, 1994.
31. Lakka, T. A., J. M. Venaliainen, R. Rauramaa, R. Salonen, J. Tuomilehto, and J. T. Salonen. Relation of leisure-time physical activity and cardiorespiratory fitness to the risk of acute myocardial infarction. N. Engl. J. Med. 330:1549-1554, 1994.
32. Lewis, C. E., C. Clancy, B. Leake, and J. S. Schwartz. The counseling practices of internists. Ann. Intern. Med. 114:54-58, 1991.
33. Lewis, B. S. and W. D. Lynch. The effect of physician advice on exercise behavior. Prev. Med. 22:110-121, 1993.
34. Mann, K. V. and R. W. Putnam. Physicians' perceptions of their role in cardiovascular risk reduction. Prev. Med. 18:54-58, 1985.
35. Manson, J. E., E. B. Rimm, M. J. Stampfer, et al. Physical activity and incidence of non-insulin-dependent diabetes mellitus in women. Lancet 338:774-778, 1991.
36. Mullen, P. and G. R. Tabak. Patterns of counseling techniques used by family practice physicians for smoking, weight, exercise and stress. Med. Care 27:694-704, 1989.
37. Nader, P. R., H. L. Taras, J. F. Sallis, and T. L. Patterson. Adult heart disease prevention in childhood: A national survey of pediatricians' practices and attitudes. Pediatrics 79:843-850, 1987.
38. National Center For Health Statistics. Health, United States, 1989, (DHHS Publication No. PHS 90-1232). Hyattsville, MD: U.S. Department of Health and Human Services, 1990.
39. Norusis, M. J. SPSS for Windows 6.0. Chicago: SPSS Inc., 1993, pp. 1-828.
40. Orleans, C. T., L. K. George, J. L., Houpt, and K. H. Brodie. Health promotion in primary care: a survey of U.S. family practitioners. Prev. Med. 14:636-647, 1985.
41. Orwin, R. G. A fail safe N for effect size in meta-analysis. J. Ed. Stat. 8:157-159, 1983.
42. Paffenbarger, R. S., Jr., R. T. Hyde, A. L. Wing, I-M. Lee, D. L. Jung, and J. B. Kampert. The association of changes in physical activity level and other lifestyle characteristics with mortality among men.N. Engl. J. Med. 328:538-545, 1993.
43. Pate, R., M. Pratt, S. B. Blair, et al. Physical activity and health: a recommendation from the Centers for Disease Control and Prevention and the American College of Sports Medicine. J.A.M.A. 273:402-407, 1995.
44. Pavlou, K. N., S. Krey, and W. P. Steffee. Exercise as an adjunct to weight loss and maintenance in moderately obese subjects.Am. J. Clin. Nutr. 49:1115-1123, 1989.
45. Powell, K. E. and S. N. Blair. The public health burdens of sedentary living habits: theoretical but realistic estimates.Med. Sci. Sports Exerc. 26:851-856, 1994.
46. Prince, R. L., M. Smith, I. M. Dick, et al. Prevention of post-menopausal bone osteoporosis. A comparative study of exercise, calcium supplementation, and hormone-replacement therapy. N. Engl. J. Med. 325:1189-1195, 1991.
47. Prochaska, J. O. and B. H. Marcus. The transtheoretical model: applications to exercise. In: Advances in Exercise Adherence, R. K. Dishman (Ed.). Champaign, IL: Human Kinetics, 1994, pp. 161-180.
48. Roback, G., L. Randolph, and B. Seidman.Physician Characteristics and Distribution in the U.S. Chicago: American Medical Association, 1993.
49. Rosenthal, R. Meta-analytic procedures for social research. Beverly Hills, CA: Sage, 1991, pp. 1-155.
50. Rosenthal, R. Parametric measures of effect size. In:The Handbook of Research Synthesis, H. Cooper and L. V. Hedges(Eds.). New York: Russell Sage Foundation, 1994, pp. 231-244.
51. Rosenthal, R. and D. B. Rubin. A simple, general purpose display of magnitude of experimental effect. J. Ed. Psychol. 74:166-169, 1982.
52. Rosenthal, R. and D. B. Rubin. Comparing effect sizes of independent studies. Psychol. Bull. 92:500-504, 1982.
53. Rosenthal, R. and D. B. Rubin. Multiple contrasts and ordered Bonferroni procedures. J. Ed. Psychol. 76:1028-1034, 1984.
54. Sallis, J. F., W. L. Haskell, S. P. Fortmann, K. M. Vranizan, C. B. Taylor, and D. S. Solomon. Predictors of adoption and maintenance of physical activity in a community sample. Prev. Med. 15:331-341, 1986.
55. Schwartz, J. S., C. E. Lewis, C. Clancy, M. S. Kinosian, M. H. Radany, and J. P. Koplan. Internists' practices in health promotion and disease prevention: a survey. Ann. Intern. Med. 114:46-53, 1991.
56. Schwarzer, R. Meta: programs for secondary data analysis, 5.3. Berlin: Free University of Berlin, 1991, pp. 1-46.
57. Sternfeld, B. Cancer and the protective effect of physical activity: the epidemiological evidence. Med. Sci. Sports Exerc. 24:1195-1209, 1992.
58. St. Jeor, S. T., K. D. Brownell, R. L. Atkinson, et al. Obesity. Workshop III. AHA Prevention Conference III. Behavior change and compliance: keys to improving cardiovascular health. Circulation 1993, pp. 88:1391-1396.
59. U.S. Department Of Health And Human Services.Healthy People 2000: National Health Promotion and Disease Prevention Objectives (DHHS Publication No. [PHS]91-50212). Washington, DC: U.S. Government Printing Office, 1991.
60. Wechsler, H., S. Levine, R. K. Idelson, M. Rohman, and J. O. Taylor. The physician's role in health promotion-a survey of primary care practitioners. N. Engl. J. Med. 308:97-100, 1983.
61. Wells, K. B., C. E. Lewis, B. Leake, M. K. Schleiter, and R. H. Brook. The practices of general and subspecialty internists in counseling about smoking and exercise. Am. J. Public Health 76:1009-1013, 1986.
62. Williford, H. N., B. R. Barfield, R. B. Lazenby, and M. Scharff Olson. A survey of physicians' attitudes and practices related to exercise promotion. Prev. Med. 21:630-636, 1992.


1. Acquista, V. W., T. J. Wachtel, C. I. Gomes, M. Salzillo, and M. Stockman. Home-based health risk appraisal and screening program. J. Comm. Health 13:43-52, 1988.

2. Allegrante, J. P., P. A. Kovar, C. R. MacKenzie, M. G. E. Peterson, and B. Gutin. A walking education program for patients with osteoarthritis of the knee: Theory and intervention strategies. Health Ed. Q. 20:63-81, 1993.

3. Allen, L. D. and B. A. Iwata. Reinforcing exercise maintenance using high-rate activities. Behav. Mod. 4:337-354, 1980.

4. Atkins, C. J., R. M. Kaplan, R. M. Timms, S. Reinsch, and K. Lofback. Behavioral exercise programs in the management of chronic obstructive pulmonary disease. J. Consult. Clin. Psychol. 52:591-603, 1984.

5. Avila, P. and M. F. Hovell. Physical activity training for weight loss in Latinas: a controlled trial. Int. J. Obesity 18:476-482, 1994.

6. Ballantyne, D. Prescribing exercise for the healthy: assessment of compliance and effects on plasma lipids and lipoproteins. Health Bull. 36:169-176, 1978.

7. Baranowski, T., B. Simons-Morton, P. Hooks, et al. A center-based program for exercise change among Black-American families. Health Ed. Q. 17:179-196, 1990.

8. Belisle, M., E. Roskies, and J. M. Levesque. Improving adherence to physical activity. Health Psychol. 6:159-172, 1987.

9. Bishop, P. and J. E. Donnelly. Home based activity program for obese children. Am. Corr. Ther. J. 41:12-19, 1987.

10. Blair, S. N., P. V. Piserchia, C. S. Wilbur, and J. H. Crowder. A public health intervention model for worksite health promotion: impact on exercise and physical fitness in a health promotion plan after 24 months.J.A.M.A. 255:921-926, 1987.

11. Blake, S. M., R. W. Jeffery, J. R. Finnegan, et al. Process evaluation of a community-based physical activity campaign: the Minnesota Heart Health Program experience. Health Ed. Res. 2:115-121, 1987.

12. Blamey, A., N. Mutrie, T. Aitchison. Health promotion by encouraged used of stairs. Br. Med. J. 311:289-290, 1995.

13. Brown, W. J. and C. Lee. Exercise and dietary modification with women of non-English speaking background: a pilot study with Polish-Australian women. Int. J. Behav. Med. 1:185-203, 1994.

14. Brownell, K., A. J. Stunkard, and J. Albaum. Evaluation and modification of exercise patterns in the natural environment. Am. J. Psychiatry 137:1540-1545, 1980.

15. Bruce, R. A., T. A. DeRouen, and K. F. Hossack. Pilot study examining the motivational effects of maximal exercise testing to modify risk factors and health habits. Cardiology 66:111-119, 1980.

16. Brynteson, P. and T. M. Adams. The effects of conceptually based physical education programs on attitudes and exercise habits of college alumni after 2 to 11 years of follow-up. Res. Q. Exerc. Sport 64:208-212, 1993.

17. Bush, P. J., A. E. Zuckerman, V. S. Taggart, P. K. Theiss, E. O. Peleg, and S. A. Smith. Cardiovascular risk factor prevention in black school children: the “Know Your Body” evaluation project. Health Ed. Q. 16:215-227, 1989.

18. Bush, P. J., A. E. Zuckerman, P. K. Theiss, et al. Cardiovascular risk factor prevention in black school children: two year results of the“Know Your Body” program. Am. J. Epidemiol. 129:466-482, 1989.

19. Calfas, K. J., B. J. Long, J. F. Sallis, W. J. Wooten, M. Pratt, and K. A. Patrick. A controlled trial of physician counseling to promote the adoption of physical activity. Prev. Med. (in press).

20. Campbell, J. The effects of a contingency managed physical fitness training program on the fitness characteristics and academic achievement of mentally retarded children. J. Spec. Ed. Mental Retard. 11:159-167, 1975.

21. Caouette, M. and G. Reid. Increasing the work output of severely retarded adults. Ed. Train. Mental Retard. 20:296-304, 1985.

22. Cardinal, B. J. and M. L. Sachs. Prospective analysis of stage-of-exercise movement following mail-delivered, self-instructional exercise packets. Am. J. Health Prom. 9:430-432, 1995.

23. Clifford, P. A., S. Y. Tan, and R. L. Gorsuch. Efficacy of a self-directed behavioral health change program: weight, body composition, cardiovascular fitness, blood pressure, health risk, and psychosocial mediating variables. J. Behav. Med. 14:303-323, 1991.

24. Coates, T. J., R. W. Jeffery, and L. A. Slinkard. Heart healthy eating and exercise: introducing and maintaining changes in health behaviors.Am. J. Public Health 71:15-23, 1981.

25. Coleman, R. S. and T. L. Whitman. Developing, generalizing, and maintaining physical fitness in mentally retarded adults: toward a self-directed program. Anal. Interv. Dev. Stud. 4:109-127, 1984.

26. Cooper, K. H., J. G. Purdy, A. Friedman, R. L. Bohannon, R. A. Harris, and J. A. Arends. An aerobics conditioning program for the Fort Worth, Texas school district. Res. Q. Exerc. Sport 46:345-350, 1975.

27. Cox, M., R. J. Shephard, and P. Corey. Influence of an employee fitness programme upon fitness, productivity, and absenteeism.Ergonomics 24:795-806, 1981.

28. Craighead, L. W. and M. D. Blum. Supervised exercise in behavioral treatment for moderate obesity. Behav. Ther. 20:49-59, 1989.

29. Crow, R., H. Blackburn, D. Jacobs, et al. Population strategies to enhance physical activity: the Minnesota Heart Health Program. Acta Med. Scand. Suppl. 711:93-112, 1986.

30. Daltroy, LH. Improving cardiac patient adherence to exercise regimens: a clinical trial of health education. J. Cardiac Rehabil. 5:40-49, 1985.

31. De Luca, R. V. and S. W. Holborn. Effects of a variable-ratio reinforcement schedule with changing criteria on exercise in obese and nonobese boys. J. Appl. Behav. Anal. 25:671-679, 1992.

32. Doleys, D. M., M. Crocker, and D. Patton. Response of patients with chronic pain to exercise quotas. Phys. Ther. 62:1111-1114, 1982.

33. Driggers, D. A., J. Swedberg, R. Johnson, et al. The maximum exercise stress test: is it a behavior-modification tool? J. Family Pract. 18:715-718, 1984.

34. Duncan, B., W. T. Boyce, R. Itami, and N. Puffenbarger. A contolled trial of a physical fitness program for fifth grade students.J. School Health 53:467-471, 1983.

35. Dwyer, T., W. E. Coonan, D. R. Leitch, B. S. Hetzel, and R. A. Baghurst. An investigation of the effects of daily physical activity on the health of primary school children in South Australia. Int. J. Epidemiol. 12:308-313, 1983.

36. Epstein, L. H., R. Koeske, and R. R. Wing. Adherence to exercise in obese children. J. Cardiac Rehabil. 4:185-195, 1984.

37. Epstein, L. H., A. M. Valoski, L. S. Vara, et al. Effects of decreasing sedentary behavior and increasing activity on weight change in obese children. Health Psychol. 14:109-115, 1995.

38. Epstein, L. H., R. R. Wing, R. Koeske, D. Ossip, and S. Beck. A comparison of lifestyle change and programmed aerobic exercise on weight and fitness changes in obese children. Behav. Ther. 13:651-665, 1982.

39. Epstein, L. H., R. R. Wing, J. K. Thompson, and W. Griffin. Attendance and fitness in aerobics exercise: the effects of contract and lottery procedures. Behav. Mod. 4:465-479, 1980.

40. Epstein, L. H., K. Woodall, A. J. Goreczny, R. R. Wing, and R. J. Robertson. The modification of activity patterns and energy expenditure in obese young girls. Behav. Ther. 15:101-108, 1984.

41. Ewart, C. K., C. B. Taylor, C. B. Reese, and R. F. DeBusk. Effects of early postmyocardial infarction exercise testing on self-perception and subsequent physical activity. Am. J. Cardiol. 51:1076-1080, 1983.

42. Farquhar, J. W., S. P. Fortmann, J. A. Flora, et al. Effects of communitywide education on cardiovascular disease risk factors: the Stanford five-city project. J.A.M.A. 51:359-365, 1990.

43. Fiatarone, M. A., E. F. O'Neill, N. D. Ryan, et al. Exercise training and nutritional supplementation for physical frailty in very elderly people. N. Engl. J. Med. 330:1769-1775, 1994.

44. Fitterling, J. M., J. E. Martin, S. Gramling, P. Cole, and M. A. Milan. Behavioral management of exercise training in vascular headache patients: an investigation of exercise adherence and headache activity.J. Appl. Behav. Anal. 21:9-19, 1988.

45. Fontana, A. F., R. D. Kerns, R. L. Rosenberg, J. L. Marcus, and K. L. Colonese. Exercise training for cardiac patients: adherence, fitness, and benefits. J. Cardiopulm. Rehabil. 6:4-15, 1986.

46. Foreyt, J. P., G. K. Goodrick, R. S. Reeves, et al. Response to free-living adults to behavioral treatment of obesity: attrition and compliance to exercise. Behav. Ther. 24:659-669, 1993.

47. Gettman, L. R., P. Ward, R. D. Hagan. A comparison of combined running and weight training with circuit weight training. Med. Sci. Sports Exerc. 14:229-234, 1982.

48. Gillett, P. A. Self-reported factors influencing exercise adherence in overweight women. Nurs. Res. 37:25-29, 1988.

49. Gillett, P. A., M. Johnson, M. Juretich, N. Richardson, L. Slagle, and K. Farikoff. The nurse as exercise leader. Geriatric Nurs. 133-137, 1993.

50. Godin, G., R. Dehsarnais, J. Jobin, and J. Cook. The impact of physical fitness and health-age appraisal upon exercise intentions and behavior. J. Behav. Med. 10:241-250, 1987.

51. Gomel, M., B. Oldenburg, J. Simpson, and N. Owen. Work-site cardiovascular risk reduction: a randomized trial of health risk assessment, education, counseling, and incentives. Am. J. Public Health 83:1231-1238, 1993.

52. Greenan-Fowler, E., C. Powell, and J. W. Varni. Behavioral treatment of adherence to therapeutic exercise by children with hemophilia.Arch. Phys. Med. Rehabil. 68:846-849, 1987.

53. Hamdorf, P. A., R. T. Withers, R. K. Penhall, J. L. Plummer. A follow-up study on the effects of training on the fitness and habitual activity patterns of 60- to 70-year-old women. Arch. Phys. Med. Rehabil. 74:473-477, 1993.

54. Heath, G. W., B. E. Leonard, R. H. Wilson, J. S. Kendrick, and K. E. Powell. Community-based exercise intervention: Zuni Diabetes Project.Diabetes Care 10:579-583, 1987.

55. Heirich, M. A., A. Foote, J. C. Erfurt, and B. Konopka. Work-site physical fitness programs: comparing the impact of different program designs on cardiovascular risks. J. Occup. Med. 35:510-517, 1993.

56. Hoyt, M. F. and I. L. Janis. Increasing adherence to a stressful decision via a motivational balance-sheet procedure: a field experiment.J. Pers. Soc. Psychol. 31:833-839, 1975.

57. Juneau, M., F. Rogers, V. De Santos, et al. Effectiveness of self-monitored, home-based, moderate intensity exercise training in middle-aged men and women. Am. J. Cardiol. 60:66-77, 1987.

58. Katz, R. C. and N. N. Singh. Increasing recreational behavior in mentally retarded children. Behav. Mod. 10:508-519, 1986.

59. Keefe, F. J. and J. A. Blumenthal. The life fitness progam: a behavioral approach to making exercise a habit. J. Behav. Ther. Exp. Psychiatry 11:31-34, 1980.

60. Kelder, S. H., C. L. Perry, and K. Klepp. Community-wide youth exercise promotion: long-term outcomes of the Minnesota Heart Health Program and the Class of 1988 study. J. School Health 63:218-223, 1993.

61. Killen, J. D., M. J. Telch, T. N. Robinson, N. Maccoby, C. B. Taylor, and J. W. Farquhar. Cardiovascular disease risk reduction for tenth graders: a multiple-factor school-based approach. J.A.M.A. 260:1728-1733, 1988.

62. King, A. C., F. Carl, L. Birkel, and W. L. Haskell. Increasing exercise among blue-collar employees: the tailoring of worksite programs to meet specific needs. Prev. Med. 17:357-365, 1988.

63. King, A. C. and L. W. Frederiksen. Low-cost strategies for increasing exercise behavior: relapse preparation training and social support.Behav. Mod. 8:3-21, 1984.

64. King, A. C., B. Frey-Hewitt, D. M. Dreon, and P. D. Wood. Diet vs exercise in weight maintenance. Arch. Intern. Med. 149:2741-2746, 1989.

65. King, A. C., W. L. Haskell, C. B. Taylor, H. C. Kraemer, and R. F. DeBusk. Group- vs home-based exercise training in healthy older men and women.J.A.M.A. 266:1535-1542, 1991.

66. King, A. C., W. L. Haskell, D. R. Young, R. K. Oka, and M. L. Stefanick. Long-term effects of varying intensities and formats of physical activity on participation rates, fitness, and lipoproteins in men and women aged 50 to 65 years. Circulation 91:2596-2604, 1995.

67. King, A. C., C. B. Taylor, W. L. Haskell, and R. F. DeBusk. Strategies for increasing early adherence to and long-term maintenance of home-based exercise training in healthy middle-aged men and women. Am. J. Cardiol. 61:628-632, 1988.

68. Knadler, G. F. and T. Rogers. “Mountain Climb Month” a low-cost exercise intervention program at a high-risk worksite. Fit. Business 10:64-67, 1987.

69. Knutsen, S. F. and R. Knutsen. The Tromso survey: the family intervention study: the effect of intervention on some coronary risk factors and dietary habits, a 6-year follow-up. Prev. Med. 20:197-212, 1991.

70. Lee, C. and N. Owen. Community exercise programs: follow-up difficulty and outcome. J. Behav. Med. 9:111-117, 1986.

71. Leppink, H. B. and A. DeGrassi. Changes in risk behavior: a two-year follow-up study. Proceeding, 13th Annual Meeting, Soc. Prospect. Med., 1977, pp. 104-107.

72. Lewis, B. S. and W. D. Lynch. The effect of physician advice on exercise behavior. Prev. Med. 22:110-121, 1993.

73. Lewis, C. B., J. M. Raczynski, G. W. Heath, R. Levinson, J. C. Hilyer, Jr., and G. R. Cutter. Promoting physical activity in low-income African-American communities: the PARR project. Ethn. Dis. 3:106-118, 1993.

74. Lindsay-Reid, E. and R. W. Morgan. Exercise prescription: a clinical trial. Am. J. Public Health 69:591-595, 1979.

75. Logsdon, D. N., M. A. Lazaro, and R. V. Meier. The feasibility of behavioral risk reduction in primary medical care. Am. J. Prev. Med. 5:249-256, 1989.

76. Lombard, D. N., T. N. Lombard, and R. A. Winett. Walking to meet health guidelines: the effect of prompting frequency and prompt structure.Health Psychol. 14:164-170, 1995.

77. Long, B. C. and C. J. Haney. Enhancing physical activity in sedentary women: information, locus of control, and attitudes. J. Sport Psychol. 8:8-24, 1986.

78. Lovibond, S. H., P. C. Birrell, and P. Langeluddecke. Changing coronary heart disease risk-factor status: the effects of three behavioral programs. J. Behav. Med. 9:415-437, 1986.

79. Luepker, R. V. Community education for cardiovascular disease prevention: risk factor changes in the Minnesota Heart Health Program.Am. J. Public Health 84:1383-1393, 1994.

80. Marcus, B. H., S. W. Banspach, R. C. Lefebvre, J. S. Rossi, R. A. Carleton, and D. B. Abrams. Using the stages of change model to increase the adoption of physical activity among community participants. Am. J. Health Prom. 6:424-429, 1992.

81. Marcus, B. H. and A. L. Stanton. Evaluation of relapse prevention and reinforcement interventions to promote exercise adherence in sedentary females. Res. Q. Exerc. Sport 64:447-452, 1993.

82. Marrero, D. G., A. S. Fremion, and M. P. Golden. Improving compliance with exercise in adolescents with insulin-dependent diabetes mellitus: Results of a self-motivated home exercise program.Pediatrics 81:519-525, 1988.

83. Martin, J. E., P. m. Dubbert, A. D. Katell, et al. The behavioral control of exercise in sedentary adults: Studies 1 through 6. J. Consult. Clin. Psychol. 52:795-811, 1984.

84. Mayer, J. A., A. Jermanovich, B. L. Wright, J. P. Elder, J. A. Drew, and S. J. Williams. Changes in health behaviors of older adults.Prev. Med. 23:127-133, 1994.

85. McAuley, E., D. S. Courneya, D. L. Rudolph, and C. L. Lox. Enhancing exercise adherence in middle-aged males and females. Prev. Med. 23:498-506, 1994.

86. McKenzie, T. L. A behaviorally-oriented residential camping program for obese children and adolescents. Ed. Treat. Child. 9:67-78, 1986.

87. McKenzie, T. L., J. F. Sallis, N. Faucette, J. J. Roby, and B. Kolody. Effects of a curriculum and inservice program on the quantity and quality of elementary physical education classes. Res. Q. Exerc. Sport 64:178-187, 1993.

88. Neale, A. V., S. P. Singleton, M. H. Dupuis, and J. W. Hess. The use of behavioral contracting to increase exercise activity. Am. J. Health Prom. 4:441-447, 1990.

89. Noland, M. P. The effects of self-monitoring and reinforcement on exercise adherence. Res. Q. Exerc. Sport 60:216-224, 1989.

90. Oldridge, N. B. and N. L. Jones. Improving patient compliance in cardiac rehabilitation: effects of written agreement and self-monitoring.J. Cardiac Rehabil. 3:257-262, 1983.

91. Ostwald, S. K. Changing employees' dietary and exercise practices: an experimental study in a small company. J. Occup. Med. 31:90-97, 1989.

92. Owen, N., A. Bauman, M. Booth, B. Oldenburg, and P. Magnus. Serial mass-media campaigns to promote physical activity: reinforcing or redundant?Am. J. Public Health 85:244-248, 1995.

93. Owen, N., C. Lee. L. Naccarella, and K. Haag. Exercise by mail: a mediated behavior-change program for aerobic exercise. J. Sport Psychol. 9:346-357, 1987.

94. Owen, N., C. Lee, and A. W. Sedgwick. Exercise maintenance: developing self-management guidelines for community fitness courses.Aust. J. Sci. Med. Sport 1:8-12, 1987.

95. Parcel, G. S., B. Simons-Morton, N. M. O'Hara, T. Baranowski, and B. Wilson. School promotion of healthful diet and physical activity: impact on learning outcomes and self-report behavior. Health Ed. Q. 16:181-199, 1989.

96. Patterson, T. L., J. F. Sallis, P. R. Nader, et al. Direct observation of physical activity and dietary behaviors in a structured environment: effects of a family-based health promotion program. J. Behav. Med. 11:447-458, 1988.

97. Perkins, K. A., S. R. Rapp, C. R. Carlson, and C. E. Wallace. A behavioral intervention to increase exercise among nursing home residents.Gerontology 26:479-481, 1986.

98. Perri, M. G. Enhancing the efficacy of behavior therapy for obesity: effects of aerobic exercise and multicomponent maintenance program.J. Consult. Clin. Psychol. 54:670-675, 1986.

99. Perry, C. L., K. I. Klepp, A. Halper, et al. Promoting healthy eating and physical activity patterns among adolescents: a pilot study of“Slice of Life.” Health Ed. Res. 2:93-103, 1987.

100. Pollock, M. L. Prescribing exercise for fitness and adherence. In: Exercise Adherence: Its Impact on Public Health, R. K. Dishman(Ed.). Champaign, IL: Human Kinetics Publishers, 1988, pp. 259-277.

101. Robison, J. I., M. A. Rogers, J. J. Carlson, et al. Effects of a 6-month incentive-based exercise program on adherence and work capacity.Med. Sci. Sports Exerc. 24:93, 1992.

102. Rowland, T. W. Motivational factors in exercise training programs for children. Physician Sportsmed. 14:122-128, 1986.

103. Sallis, J. F., T. L. McKenzie, J. A. Alcaraz, B. Kolody, N. Faucette, and M. F. Hovell. Effects of a two-year health-related physical education program on physical fitness and activity in elementary school students: SPARK. Am. J. Public Health (in press).

104. Shephard, R. J. Twelve years experience of a fitness program for the salaried employees of a Toronto Life Assurance Company. Am. J. Health Prom. 6:292-310, 1992.

105. Shephard, R. J., J. JeQuier, H. Lavallee, R. La Barre, and M. Rajic. Habitual physical activity: effects of sex, milieu, season and required activity. J. Sports Med. Phys. Fitness 20:55-66, 1980.

106. Shephard, R. J. and H. Lavallee. Impact of enhanced physical education in the prepubescent child: Trois Rivieres revisited. Pediatr. Exerc. Sci. 5:177-189, 1993.

107. Siegel, J. A. and T. G. Manfredi. Effects of a ten-month fitness program on children. Physician Sportsmed. 12:91-97, 1984.

108. Simons-Morton, B. G., G. S. Parcel, T. Baranowski, R. Forthofer, and N. M. O'Hara. Promoting physical activity and a healthy diet among children: results of a school-based intervention study. Am. J. Public Health 81:986-991, 1991.

109. Slava, S., D. R. Laurie, and C. B. Corbin. Long-term effects of a conceptual physical education program. Res. Q. Exerc. Sport 55:161-168, 1984.

110. Spink, K. S. and A. V. Carron. The effects of team building on the adherence patterns of female exercise participants. J. Sport Exerc. Psychol. 15:39-49, 1993.

111. Stainback, S., W. Stainback, P. Wehman, and L. Spangiers. Acquisition and generalization of physical fitness exercises in three profoundly retarded adults. T.A.S.H. J. 8:47-55, 1983.

112. Suter, E., B. Marti, and F. Gutzwiller. Jogging or walking: comparison of health benefits. Ann. Epidemiol. 4:375-381, 1994.

113. Taggart, A. C., J. Taggart, D. Siedentop. Effects of a home-based activity program: a study with low fitness elementary school children.Behav. Mod. 10:487-507, 1986.

114. Tell, G. S. and O. D. Vellar. Noncommunicable disease risk factor intervention in Norwegian adolescents: the Oslo Youth Study. In:Cardiovascular Risk Factors in Children: Epidemiology and Prevention, B. Hetzel and G. S. Berenson (Eds.). New York: Elsevier Science Publishers, 1987, pp. 203-217.

115. Thompson, C. E. and L. M. Wankel. The effects of perceived activity choice upon frequency of exercise behavior. J. Appl. Soc. Psychol. 10:436-443, 1980.

116. Tu, J. and A. Rothstein. Improvement of jogging performance through application of personality specific motivational techniques.Res. Q. Exerc. Sport 50:97-103, 1979.

117. Van Deusen, J. and D. Harlowe. A comparison of the ROM dance home exercise/rest program with traditional routines. Occup. Ther. J. Res. 7:349-361, 1989.

118. Vuori, I., P. Oja, and O. Paronen. Physically active commuting to work: testing its potential for exercise promotion. Med. Sci. Sports Exerc. 26:844-850, 1994.

119. Walter, H. J., A. Hofman, R. D. Vaughan, and E. L. Wynder. Modifications of risk factors for coronary heart disease. N. Engl. J. Med. 318:1093-1100, 1988.

120. Wankel, L. M. and C. Thompson. Motivating people to be physically active: self-persuasion vs. balanced decision making. J. Appl. Soc. Psychol. 7:332-340, 1977.

121. Wankel, L. M., J. K. Yardley, and J. Graham. The effects of motivational interventions upon the exercise adherence of high and low self-motivated adults. Can. J. Appl. Sport Psychol. 10:147-156, 1985.

122. Weber, J. and H. Wertheim. Relationships of self-monitoring, special attention, body fat percent, and self-motivation to attendance at a community gymnasium. J. Sport Exerc. Psychol. 11:105-114, 1989.

123. Wier, L. T., A. S. Jackson, and M. B. Pinkerton. Evaluation of the NASA/JSC health related fitness program. Aviat. Space Environ. Med. 60:438-444, 1989.

124. Wiggam, J., R. French, and H. Henderson. The effects of a token economy on distance walked by senior citizens in a retirement center.Am. Corr. Ther. J. 40:6-12, 1986.

125. Wild, B., C. Smith, J. Martin, and M. Shook. Worksite and community health promotion/risk reduction project: Virginia, 1987-1991.MMWR 41:55-57, 1992.

126. Wysocki, T., G. Hall, B. Iwata, and M. Riordan. Behavioral management of exercise: contracting for aerobic points. J. Appl. Behav. Anal. 12:55-64, 1979.

127. Young, D. R., W. L. Haskell, C. B. Taylor, and S. P. Fortmann. Effect of community health education on physical activity knowledge, attitudes and behavior: the Stanford Five-City Project. Am. J. Epidemiol. (in press).



©1996The American College of Sports Medicine