Authors
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Martin Ginis K.A., Townson A., Martin Ginis K.A., Hoekstra F., Baumgart J.K., Little J.P., Todd K.R., Martin Ginis K.A., Gee C., Hoekstra F., Baumgart J.K., Todd K.R., Townson A., West C.R., Kramer J.L.K., Martin Ginis K.A., Hoekstra F., Baumgart J.K., Davis J.C., Little J.P., West C.R., Gee C., Blitz S., Karim M.E., Singer J., Baumgart J.K., Davis J.C., Davis J.C., Karim M.E., Singer J., West C.R., Kramer J.L.K., Kramer J.L.K. -More
Category
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Primary study
Journal»Arch. Phys. Med. Rehabil.
Year
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2026
OBJECTIVE: To test the hypothesis that home- and community-based exercise, prescribed according to the spinal cord injury (SCI) exercise guidelines, reduces chronic pain.
DESIGN: Single-blinded, pragmatic randomized controlled trial with 2 arms (exercise intervention, waitlist control) and assessments at baseline, 3 months, and 6 months.
SETTING: Testing at 2 university-based laboratories located on separate campuses within the same institution. Exercise in participants' preferred locations.
PARTICIPANTS: Forty-six adults with SCI (76% men/male; 59% paraplegic; Mage=50.6±14.1; Myears since injury=16.5±12.8) and chronic neuropathic or musculoskeletal pain, who did not routinely achieve the SCI exercise guidelines.
INTERVENTION: Intervention participants (n=25) received an individualized exercise prescription for aerobic and strength training. Fitness trainers and exercise counselors supported implementation. Control participants (n=21) continued their usual activities.
MAIN OUTCOME MEASURES: The primary outcome was the SF-36 Pain score at 6 months. Secondary outcomes were International SCI Pain Basic Dataset version 2.0 (ISCIPBDS) pain-intensity and interference scores, and standardized measures of pain coping, well-being, conditioned pain modulation, and proinflammatory cytokines.
RESULTS: In intent-to-treat analyses, the estimated treatment effect (95% CI) on SF-36 Pain was 7.9 (-1.9 to 17.7; P=.11) at 6 months. Tipping-point analyses suggested that these effects may have been significant if the target sample size had been achieved. Treatment effects for ISCIPBDS pain intensity were -1.8 (-3.4, -0.1; P=.04) at 6 months. Relative to controls, participants in the intervention condition reported significant reductions in pain interference at 3 months and reduced use of pain-coping strategies at 6 months (Ps<0.05). No other effects were significant.
CONCLUSIONS: Intervention effects on SF-36 Pain were inconclusive. Analyses of secondary outcomes (ISCIPBDS) suggest exercise prescribed according to the SCI exercise guidelines, and implemented in real-world settings, can reduce pain intensity. Meeting the aerobic-exercise guideline may be especially important. Further replication in pragmatic trials is required.
Epistemonikos ID: ef37a80201f148524837fd7440cc35b3a2f84e37
First added on: Jun 18, 2026