Resistance Exercise, Disability, and Pain Catastrophizing in Obese Adults with Back Pain : Medicine & Science in Sports & Exercise

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Resistance Exercise, Disability, and Pain Catastrophizing in Obese Adults with Back Pain


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Medicine & Science in Sports & Exercise 46(9):p 1693-1701, September 2014. | DOI: 10.1249/MSS.0000000000000294
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Pain-related fear and fear avoidance are psychosocial factors that are strongly related to long-term disability in persons with chronic low back pain (LBP) (1,2). However, the relations between pain-related fear, chronic LBP, and physical function in the obese, older adult are not known. The national obesity crisis is continuing, concurrent with the increased prevalence of LBP (34) and physical disability, especially in the older demographic. Because the current socioeconomic effect of chronic LBP is large (9), the additive burdens of obesity and LBP will further strain availability of health care resources. The lack of understanding of the relations between perceived disability, fear avoidance, and painful movement and potential interventions to address these factors are therefore a serious scientific deficit.

Previous studies that examined exercise interventions for back pain in this population have largely focused on the physical outcomes or pain symptoms and less so on fear avoidance beliefs or pain catastrophizing. The levels of fear of movement among nonobese and obese persons who sought physical therapy for LBP have been characterized (39). Fear avoidance beliefs were moderately elevated in obese, middle-age individuals compared with those in their nonobese counterparts, and higher kinesiophobia levels were associated with higher disability scores in obese persons compared with those in nonobese counterparts (39). Reducing pain-related fear avoidance beliefs and catastrophizing might be an underexamined strategy to prevent disability in the obese, older adult. Furthermore, it has been shown that total body resistance exercise (including a lumbar extension exercise) improved low back strength in older, overweight adults (41). Other studies have shown that different resistance exercise programs can reduce LBP symptoms (3,16,17,26,30). Resistance exercise also results in favorable psychosocial benefits such as reduction of anxiety and fear of falling, both of which can contribute to increased physical function and activity (19,22). It is unclear, however, if resistance exercise protocols reduce perceived disability due to LBP, fear avoidance beliefs, and pain catastrophizing in the obese, older adult. Because earlier studies have used a variety of different resistance exercise protocols (isokinetic or dynamic machines and free weights or body weight) and many have not focused on the obese, older population, it is not clear which specific components of exercise therapy are most effective in reducing pain and in minimizing the negative psychological effects such as pain catastrophizing. Therefore, the purpose of this study was to determine whether changes in fear avoidance beliefs, kinesiophobia, or pain catastrophizing contributed to the changes in perceived disability due to LBP with either lumbar extension resistance exercise training or total body resistance training. A secondary purpose was to determine whether either lumbar extension resistance exercise training or total body resistance training decreased disability due to back pain or pain with movement.



Older adults with chronic LBP were recruited from the Gainesville area and surrounding regions using the University of Florida (UF) Orthopaedics Clinics, the Clinical Trials Register, study flyers, newspaper advertisements, and a list of older adults provided by the UF Claude Pepper Aging Center from the time frame of December 2010 to August 2012.

Inclusion criteria

Men and women 60–85 yr of age, experiencing LBP for ≥6 months (12), with abdominal obesity, and free of abnormal cardiovascular responses during ECG screening tests were eligible for the study. Exclusion criteria included being wheelchair bound, regular resistance training (participating in resistance exercise three or more times per week within the last 6 months), presence of specific LBP due to an acute back injury such as a lumbar disc herniation or rupture (12), spinal stenosis with neurogenic claudication, back surgery within the previous 2 yr (12), and the use of weight loss medication. LBP eligibility criteria were first reviewed on each potential participant by the study coordinator and next reviewed by the physicians on the study to ensure that appropriate participants were enrolled. This study was approved by the UF institutional review board, and all procedures on human subjects were conducted in accordance with the Helsinki Declaration of 1975, as revised in 1983. All participants provided a written informed consent. The study was registered as a clinical trial (NCT01250262). The study flow diagram is shown in Figure 1.

Study flow diagram.

A core group of coordinators and trained exercise physiologists conducted the testing sessions and assessments for the study. The physiologists and the physicians who provided coverage and interpretation of the testing were blinded to the randomization, group assignment, and interventions. However, all members of the study team were aware of the screening procedures as part of the study design.

Psychological Assessment

Three scales (Tampa Scale of Kinesiophobia (TSK), Fear Avoidance Beliefs Questionnaire (FABQ), and Pain Catastrophizing Scale (PCS)) were the primary outcomes and were used to measure changes in psychological characteristics over 4 months. The TSK was used to measure fear of movement or reinjury in patients with chronic pain. The modified version of the TSK (composed of 11 questions, TSK-11) was used in this study because of the invariant nature of the instrument across conditions and patient populations. Each item is provided with a 4-point Likert scale with scoring alternatives ranging from “strongly disagree” to “strongly agree” (47). The TSK has been validated for use in patients with chronic LBP (42). This instrument is characterized by two lower-order factors (somatic focus and activity avoidance focus) (27). The “somatic focus” represents the beliefs of underlying and serious medical problems, and the “activity avoidance focus” represents the belief that participation in activity could result in (re)injury or increased LBP (27). These two lower-order factors and the overall TSK score are presented in the Results. The FABQ is a tool based on theories of fear and avoidance behavior and focuses specifically on beliefs about how physical activity and work affect LBP (45). The FABQ consists of two scales: a four-item FABQ physical activity scale and a seven-item work scale. These scales will be reported separately, as has been described (8). Internal consistency of the TSK and FABQ scores ranges from α = 0.70 to α = 0.83 in persons with LBP (37). The PCS (36) is a 13-item scale that assessed the effect of chronic back pain on rumination on pain symptoms and helplessness. Pain catastrophizing is the tendency to focus on and amplify pain sensations and feel helpless when pain occurs. For all instruments, higher scores represent greater fear of movement, fear avoidance beliefs, and pain catastrophizing.

Perceived disability due to back pain

Two surveys were secondary outcomes and were used to assess self-report of disability due to LBP: the modified Oswestry Disability Index (ODI) (6) and the Roland Morris Disability Questionnaire (RMDQ) (28). The modified version of the ODI is responsive to intervention treatments for LBP, is reliable with an intraclass coefficient value of 0.90, and corresponds well with several global patient disability measures (6,28). The RMDQ assesses physical disability and mental function with LBP; this survey is sensitive to treatment interventions, is reproducible (test–retest correlations, 0.83–0.91) and consistent (Cronbach α = 0.84–0.91), and correlated well with other global ratings and disability measures (28).

Pain Assessments

Back pain severity with movement(s) was a secondary outcome and was self-reported using an 11-point numerical pain rating scale (NRSpain) with terminal descriptors (anchors of 0 = no pain, 10 = worst possible pain). The NRSpain measure is an established, well-accepted outcome for chronic pain conditions, as described in the Initiative on Methods, Measurement, and Pain Assessment in Clinical Trials (5). This measurement is reliable and valid (44) for assessing pain intensity. NRSpain measures were collected pretraining at baseline and at month 4 after the training intervention. Participants rated their back pain while rising from a chair, while climbing a set of stairs, and while walking on a level surface. Three trials of each activity were performed, and pain ratings were collected during each trial. The average of the pain ratings was the functional pain score for that activity.

Resistance Exercise Interventions

Participants were randomly and equally assigned to one of three study groups: a total body resistance exercise group (TOTRX, includes lumbar extension), an isolated lumbar extension resistance exercise group (LEXT), or a non-exercise control group (CON). A computer-generated list was used to randomly assign the group allocation; the assignments per participant number were placed in numbered sealed envelopes, and each new enrolled participant opened an envelope to receive the group assignment. One study coordinator issued the assignment, and the principal investigator and other investigators were blinded to the allocation sequence. All exercises were performed on dynamic resistance exercise machines (MedX®). Exercise training sessions were performed in a supervised laboratory setting over a 4-month period. Before any study measures were collected, all participants were familiarized with all the testing equipment and performed a light exercise set on each of the exercise machines to determine seat adjustments and customize positioning. Details of each exercise session such as repetitions, load, and perceived effort were recorded in a personalized training chart. Participants in the trained groups reported to the laboratory three times a week for one-on-one training sessions with an experienced exercise physiologist. Resistance loads were set using a percentage of the one-repetition maximum (1RM) technique for each exercise (34). For each exercise, a warm-up of five repetitions at a low weight was followed by three repetitions at a higher weight of each dynamic exercise. One lift was performed at progressively higher loads until the dynamic exercise could not be performed or was performed with good form. 1RM values were secondary outcomes. Recovery periods between each left lasted 60 s. In our laboratory, the reliability of this technique is very high (Cronbach α range, 0.92–0.98). Using this technique, no adverse events (AE) occurred. Participants performed the training program in the same laboratory as the one where the testing occurred. Partitioned areas in the laboratory permitted multiple tests and training to occur at the same time. Participants were provided standardized training and were escorted to and from the training areas. Specific training times were established for each participant during the week to avoid exposure to other participants and contamination of data. AE were tracked during the study. Any AE (whether directly related to the study or not) or unintended effects were documented from the time of enrollment to completion of the 4-month study for each participant and were reviewed as they occurred, on a monthly basis with the study team.

Total body resistance exercise (TOTRX)

For the TOTRX group, one set of each exercise was completed during each training session: leg press, leg curl, leg extension, chest press, seated row, overhead press, triceps dip, lumbar extension, biceps curl, calf press, abdominal curl, and the same lumbar extension exercise to be described later. Each set contained 15 repetitions performed at a resistance load of 60% of the 1RM for that exercise to reduce the risk of injury. Participants subjectively rated the effort of the exercise set using the 6- to 20-point Borg scale (where 6 = no muscle effort at all and 20 = maximal muscle effort possible) (40). The resistance load was increased by approximately 2% per week for the set to maintain a relative level of muscle effort at approximately 16–18 for the exercise over time (40). This was monitored by monthly assessment of 1RM values to ensure that an increase was occurring at the anticipated rate for this group.

Lumbar extension resistance exercise (LEXT)

During the first 2 wk, participants performed two sets of lumbar extensions once a week as they acclimated to the exercise (15 repetitions until volitional fatigue). From week 2 until the end of the study, participants performed one set of lumbar extensions (15 repetitions) three times a week. Similar to the TOTRX group, the resistance load for the LEXT was set at 60% 1RM and was increased by approximately 2% per week for the set to maintain a relative level of muscle effort at approximately 16–18 for the exercise over time. The frequency for the LEXT was selected on the basis of previous works, which have shown inconsistent improvements in functional changes and lumbar muscle cross-sectional area and self-reported functional improvement with training frequencies less than three times a week (11,21,33,46). The frequency of contact times was also chosen to match that of the TOTRX group between the study team and the participants. This was monitored by monthly assessment of 1RM values to ensure that an increase was occurring at the anticipated rate for this group.

Nonexercise, standard care (CON)

The CON group consisted of participants who received normal medical care and follow-up during the 4-month study, with no resistance exercise intervention. Educational recommendations from the Centers for Disease Control and Prevention and the American Heart Association regarding physical activity and diet were provided and reviewed with each participant as part of standard care. Administration of guidelines such as these has been used in control groups in similarly designed exercise studies (29). Materials included information on and demonstrations of strengthening body weight-based exercise for back health and healthy nutritional choices and information about back pain. These same educational materials given to the CON group were also provided to the participants in the two training groups. Control participants were offered the opportunity to complete a total body resistance exercise program after the control period. Participants visited the testing laboratory once a month for surveys and strength testing.

Sample Size Estimation

Power analysis was calculated using previously published data regarding differences elicited in subjective lumbar pain ratings, the primary outcome measure, between control groups and MedX® resistance exercise in persons with chronic LBP (26). The self-reported pain rating was chosen because it is a major factor affecting fear avoidance beliefs and other outcome variables in the study and is sensitive to change with lumbar strengthening interventions (13,26). Although some studies have shown 30%–60% reductions in lumbar pain with isolated lumbar exercise (13,20), these studies did not have a control group for comparison. The results from a randomized, controlled short-term study using adults with chronic back pain who participated in lumbar training revealed that self-reported pain values of the resistance exercise group were 3.4 points (baseline) and 2.9 points (posttraining) versus the standard care, nonexercise group of 3.7 points (baseline) and 4.1 (posttraining) with pooled SD of 1.6 points at baseline and 1.6 points posttraining (26). These improvements were accompanied by improvements in self-reported disability and physical function. The power analysis revealed that a total sample size of 48 participants (n = 16 per group) would yield 85% power to detect these differences between groups at α level of 0.05. In our earlier study of resistance exercise in overweight, older adults, the average dropout rate was 25% (41). Therefore, the sample size has been increased to 20 persons per group for a total of 60 participants. Participants will be randomly assigned with equal probability to one of the three study groups: 1) standard care control (CON), 2) isolated lumbar resistance exercise (LEXT), or 3) total body resistance exercise (TOTRX). Potential confounders that might have contributed to changes in the primary outcomes included changes in habitual physical activity (tracked using a dual-axis accelerometer over 7 days (SAM; Cyma, Seattle, WA) at baseline and month 4 and changes in pain medication use (number of pain medications used on a daily basis for chronic LBP monitored every 4 wk).


Statistical analyses were performed using the Statistical Package for the Social Sciences (version 21.0). Data were managed using Research Electronic Data Capture (10). Descriptive statistics and frequencies were obtained to characterize the study groups. Normality of the data was examined with Kolmogorov–Smirnov tests. Nonparametric methods were applied if data fell outside the normal distribution. Nonparametric tests (Kruskal–Wallis tests) were used to determine whether differences existed among the groups for categorical baseline variables and the study outcome measures. The between-subject factor was study group (CON, LEXT, and TOTRX), and the within-subject variables were psychological survey responses. Repeated-measures ANOVA were performed on the secondary continuous variables of maximal strength to determine whether group–time interactions occurred. Secondary variables were pain with movement scores, perceived disability scores, 1RM values, and potential confounders such as change in daily activity and pain medication number. The between-subject factor was the treatment group (CON, LEXT, and TOTRX), and the within-group factor was time (baseline and month 4). Correlations were performed between the change scores in pain catastrophizing and the change scores in fear avoidance belief scores (work and activity), ODI, and the RMDQ. A Bonferroni correction was used to account for multiple comparisons. To determine whether the changes in scores of PCS, FABQ, and TSK contributed to the change scores in self-reported disability (ODI and RMDQ), hierarchical regression models were generated. The models were generated by first entering factors that might have contributed to the disability score changes (age, sex, and race) and the change in lumbar strength from baseline to month 4. The PCS, FABQ, and TSK scores were then added to the models. Different models were generated for each disability score. Significance was established at P < 0.05 for all statistical tests.


Participant characteristics

Figure 1 shows the study flow diagram. A total of 196 people were screened by phone, and 124 candidates did not meet all the inclusion criteria or met one or more exclusion criteria. Baseline participant characteristics are shown in Table 1. There were no differences in the physiological characteristics among the three study groups.

Baseline characteristics of the study groups.

Habitual physical activity levels were monitored for all participants, and medication number and type were documented at baseline, monthly, and at month 4. The changes in the daily steps taken per day at baseline and month 4 were 3888 ± 1974 to 4106 ± 1800 steps (CON), 3607 ± 1748 to 3470 ± 1739 steps (LEXT), and 3730 ± 1455 to 3289 ± 1148 steps (TOTRX), respectively (P = 0.584). Pain medication number decreased in the TOTRX compared with that in the CON group from baseline to month 4 (1.9 ± 1.0 to 0.8 ± 0.8 medications vs 1.3 ± 0.7 to 1.3 ± 1.0 medications, respectively, P < 0.05). The change in medication number did not achieve significance in the LEXT group over the 4-month study (1.6 ± 1.0 to 1.1 ± 1.1 medications). The number of patients experiencing any AE was 8/22 enrolled in the TOTRX and 3/20 enrolled in the LEXT compared with 0 in the CON group. The proportion of patients experiencing a severe AE, as judged by the investigators, was similar between the training groups (9% in TOTRX and 10% in LEXT), and these were anticipated AE and not related to the study (worsening of back pain that required medical intervention).

The adherence to the study testing visits was 100% in all groups, and the percentage of exercise training sessions completed was 87% in both of the LEXT and TOTRX groups. Maximal strength (1RM values) significantly improved for key exercises such as lumbar extension and leg press by month 4 (P < 0.05) (Table 2). Although there were improvements in the chest press in the TOTRX group, these did not reach significance (P = 0.06).

1RM values for key exercises before and after the 4-month intervention.

Survey responses

The responses to the perceived disability, fear avoidance, and pain catastrophizing surveys are shown in Table 3. There was a significant group–time interaction for the ODI scores and the RMDQ scores (both P < 0.05). The TOTRX group demonstrated the greatest reduction in perceived disability due to LBP among the three study groups by month 4 for both surveys. There was a significant group–time interaction for the PCS scores (P < 0.05), where the TOTRX group demonstrated the greatest reduction in pain catastrophizing among the three study groups by month 4. There were no significant group–time interactions for the TSK or FABQ scores.

Perceived disability, fear avoidance beliefs, and pain catastrophizing scores at baseline and month 4.

There were significant correlations between the changes in PCS scores and the changes in FABQ activity scores (r = 0.442, P = 0.001), in the ODI (r = 0.350, P = 0.01), and in pain with walking (r = 0.35, P = 0.014). The correlations between the change in PCS and the change in the RMDQ scores (r = 0.320, P = 0.025) or the change in resting pain (r = 0.19, P = 0.18) did not achieve significance.

Pain with movement

Pain severity was assessed during chair rise, stair climbing, and walking tasks. Baseline pain scores were in the mild-to-moderate range (Table 4). The absolute pain scores and the percentage change in pain from baseline to month 4 are presented in Table 4. Pain with chair rise was significantly decreased in the TOTRX group compared with that in the other two groups. Pain during walking was significantly decreased in the TOTRX and LEXT groups compared with that in the CON group.

Pain severity ratings during movement.


Table 5 provides the results of the hierarchical regression analyses. Among the change scores for PCS, FABQ work and activity, and TSK, only PCS significantly contributed to the variance of the models for the ODI scores and RMDQ scores (P < 0.05).

Hierarchical regression analyses for the changes in self-reported disability scores and ODI and RMDQ scores.


The purpose of this study was to compare the effects of two different resistance exercise protocols on fear avoidance beliefs, perceived disability, and back pain symptoms in obese, older adults with LBP. A secondary purpose was to determine whether changes in FABQ, TSK, or PCS scores contributed to the changes in perceived disability due to LBP. There were three main findings of this study. First, TOTRX was more efficacious than LEXT in reducing self-reported disability scores due to back pain (ODI, RMDQ) compared with LEXT. Second, pain catastrophizing levels decreased with resistance exercise, with concomitant reductions in self-reported disability values in the TOTRX group relative to the CON group. The change in PCS scores from baseline to month 4 corresponded with changes in self-reported disability due to back pain and pain with walking. Third, pain severity with the performance of activities of daily living was reduced by TOTRX and LEXT.

The finding that pain catastrophizing, but not other factors, emerged as a psychological factor that could be improved with exercise could be due to obesity itself. For example, severely obese persons with other joint pain (e.g., knee osteoarthritis) demonstrate approximately 30% higher average pain catastrophizing scores compared with that in overweight persons (32). Other studies in overweight and obese persons with osteoarthritis show that higher pain catastrophizing leads to greater physical disability via lowered self-efficacy for physical function (31). The fear avoidance model suggests that catastrophizing about pain initiates a debilitating cycle of pain-related fear, impairment, and disability (43). An interpretation of our findings relative to this model is that short-term resistance exercise reduces pain catastrophizing, and additional training time may be required to alter the next stages of the fear avoidance cycle including kinesiophobia and the fear avoidance beliefs. Because we did not induce weight loss in this study, there could be remaining posttraining mobility challenges or mild pain that require additional time to overcome.

Although there are no direct comparative studies in this population at present, comprehensive rehabilitation programs in adults that have combined exercise with cognitive behavioral therapies can elicit reductions in RMDQ scores, TSK scores, and NRSpain scores that can be maintained as long as 2 yr (23). Reductions in the RMDQ ranged from 15.3 to 1.4 points (rehabilitation) versus 15 to 11 points (control); the TSK score was reduced from 42 to 17.7 points (rehabilitation) and from 41 to 40.9 points (control) (23). Workplace interventions for back pain 2 months in duration that include strength training can reduce TSK scores by approximately 10%, with reductions in NRSpain score by approximately 39% (24). Other comparative intervention studies of physiotherapy, aerobic activity, and muscle reconditioning with isoinertial loading have shown that although all groups demonstrated a reduction in NRSpain scores, RMDQ scores were improved most in the aerobics and isoinertial loading groups (16%–18% improvement) (20). Our improvements of approximately 4–11 points in the TSK in obese, older adults, RMDQ, and ODI are within the ranges of those presented in previous studies.

Published evidence shows that both high- and low-intensity lumbar extensor training programs (using a similar lumbar extension machine to that used in the present study) decreased TSK scores, but not RMDQ and ODI scores, from 4.3% to 12%, respectively, over 9 months of training (12). Another study used a quota-based course of rehabilitation for chronic LBP and measured self-reported disability, pain, and kinesiophobia (18). Each patient completed an average of 14 therapy visits and performed resistance exercise, flexibility, and lifting activities. After the program, ODI, TSK, and FABQ scores all improved; at a 12-month follow-up, all the improvements in these measures were maintained. Of relevance to our obese cohort with back pain, 12 wk of limited range of motion of lumbar extension resistance exercise reduced NRSpain values less than full range of motion (−30.3 mm vs −16.3 mm) but was shown to generate similar reductions in ODI scores (−18.2 points vs −12 points) (33). Many obese participants are unable to complete a full lumbar flexion-to-extension motion similar to that of nonobese persons. These previously published data show that strength exercise for the lumbar muscles in a limited range of motion can help reduce back pain severity even in persons with large waistline and restricted trunk flexion/extension motion.

The clinical relevance of a reduction in pain catastrophizing with resistance exercise in the obese, older adult is the potential for increased tolerance to physical activity and increased self-efficacy for physical function. Pain catastrophizing is a modifiable pain condition (38). The reduction of pain catastrophizing is thus an appropriate treatment target because the measure is related to reductions in ambulatory pain severity and perceived disability. Achieving high-quality mobility (low-pain or pain-free movement) is a primary goal for this population. The resistance exercise protocols in this study provided the opportunity for these participants to perform physical activities and exercises that they feared would aggravate pain. Progressive resistance exercise helped to reduce pain severity with specific activities such as chair rise and walking. In the fear avoidance model of chronic LBP, pain catastrophizing is the first step in the negative path of physical activity intolerance (35), fear, fear avoidance, disuse, and disability (43). Decreasing pain catastrophizing levels may help obese, older adults with back pain reconsider the harmfulness of the pain and develop confidence in overperforming physical activities that may help them achieve life goals (4), such as becoming physically active. We speculate that this positive change in psychological outlook may therefore facilitate regular participation in other exercise programs and activity for weight management.

Limitations and strengths

Several limitations of the study should be mentioned. First, the results presented here are largely from Caucasian participants, and additional work should be performed in other races to improve generalization. Data show that African Americans with chronic pain have different rehabilitation outcomes from those in Caucasians (7,14) and Asians (Chinese) have higher pain catastrophizing and pain severity than those in European Canadians (15). Second, LBP severity at enrollment was not controlled. Participants had variations in the average LBP value, ranging from mild to severe. It is possible that the initial pain severity level influenced perceived disability (25) and responsiveness to the resistance exercise protocols. Larger studies might consider performing exercise interventions in persons with mild, moderate, and severe chronic LBP and evaluating changes in pain and perceived disability. Third, these resistance exercise interventions were relatively short-term interventions, and future investigations may consider which resistance exercise program characteristics (exercise set structure and frequency per week) can maintain improvements in psychosocial status over the long term. Fourth, the finding that the CON group demonstrated some improvement in 1RM strength for the leg press and the lumbar extension was unanticipated. Given that the control participants did not increase habitual physical activity and did not report starting any new exercise programs during the study, it is possible that with the monthly 1RM testing and repeated exposures to the machines, some of these controls may have simply felt more comfortable fully engaging in the strength test knowing that their backs would not be injured because of the test. Finally, the applicability of these findings to other populations with back pain or chronic musculoskeletal pain should be tested. The strengths included a study design that was in accordance with the Consolidated Standards of Reporting Trials statement to optimize internal validity and reduce any bias. Adherence to the training programs in both LEXT and TOTRX groups was excellent. The study used well-established and validated survey instruments (5,36,37) to examine changes in fear avoidance beliefs and pain.


Total body resistance exercise (including lumbar extension exercise) was more effective than lumbar extension exercise alone in reducing self-reported disability scores due to back pain. Pain catastrophizing levels decreased with TOTRX, with concomitant reductions in self-reported disability values relative to the CON group. Pain severity was reduced in the TOTRX group during chair rise activity, and walking pain severity was decreased in both LEXT and TOTRX groups relative to the CON group. Practitioners should include resistance exercise programs that include lumbar extension to help treat obese, older adults with chronic LBP.

Research reported in this publication was supported by the National Institute of Arthritis and Musculoskeletal and Skin Diseases of the National Institutes of Health under award number AR057552-01A1. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. This work supported in part by the NIH/NCATS Clinical and Translational Science Award to the University of Florida, UL1 TR000064.

The authors declare no conflicts of interest.

The results of this study do not constitute endorsement by the American College of Sports Medicine.


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