Taking ACTION to Reduce Pain: a Randomized Clinical Trial of a Walking-Focused, Proactive Coaching Intervention for Black Patients with Chronic Musculoskeletal Pain.
Study Goal
The researchers aimed to determine whether a walking-focused, proactive coaching intervention could improve chronic pain outcomes among Black patients compared to usual care.
Results Summary
The intervention did not produce statistically significant improvements in the primary outcome (pain-related physical functioning) but showed modest improvements in pain intensity, interference, and global impression of change at 3 and 6 months.
Population
Black patients at the Atlanta VA Health Care System with moderate to severe chronic back, hip, or knee pain.
Effective Dosage
Six telephone coaching sessions over 8-14 weeks.
Duration
6 months (primary outcome assessment).
Interactions
None mentioned
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
Six telephone coaching sessions over 8-14 weeks, proactively delivered, using action planning and motivational interviewing to increase walking | no change | 30% improvement in pain-related physical functioning (Roland Morris Disability Questionnaire [RMDQ]) | Black patients at the Atlanta VA Health Care System with moderate to severe chronic back, hip, or knee pain | 32.4% of intervention participants had 30% improvement on the RMDQ vs. 24.7% of patients in usual care; aOR=1.61, 95% CI, 0.94 to 2.77 | did not produce statistically significant effects on | #1 |
Six telephone coaching sessions over 8-14 weeks, proactively delivered, using action planning and motivational interviewing to increase walking | no change | other secondary outcomes assessed at 6 months | Black patients at the Atlanta VA Health Care System with moderate to severe chronic back, hip, or knee pain | - | did not produce statistically significant effects on | #2 |
Six telephone coaching sessions over 8-14 weeks, proactively delivered, using action planning and motivational interviewing to increase walking | decrease | pain relative to usual care | Black patients at the Atlanta VA Health Care System with moderate to severe chronic back, hip, or knee pain | mean difference=-0.54, 95% CI, -0.85 to -0.23 | reported more favorable changes in | #3 |
Six telephone coaching sessions over 8-14 weeks, proactively delivered, using action planning and motivational interviewing to increase walking | decrease | pain intensity and pain interference over 3 months | Black patients at the Atlanta VA Health Care System with moderate to severe chronic back, hip, or knee pain | mean difference=-0.55, 95% CI, -0.88 to -0.22 | experienced a significant reduction in | #4 |
BACKGROUND: Black patients in the USA are disproportionately affected by chronic pain, yet there are few interventions that address these disparities. OBJECTIVE: To determine whether a walking-focused, proactive coaching intervention aimed at addressing contributors to racial disparities in pain would improve chronic pain outcomes among Black patients compared to usual care. DESIGN: Randomized controlled trial with masked outcome assessment ( Clinicaltrials.gov : NCT01983228). PARTICIPANTS: Three hundred eighty Black patients at the Atlanta VA Health Care System with moderate to severe chronic back, hip, or knee pain. INTERVENTION: Six telephone coaching sessions over 8-14 weeks, proactively delivered, using action planning and motivational interviewing to increase walking, or usual care. MAIN MEASURES: Primary outcome was a 30% improvement in pain-related physical functioning (Roland Morris Disability Questionnaire [RMDQ]) over 6 months among Black patients, using intention-to-treat. Secondary outcomes were improvements in pain intensity and interference, depression, anxiety, global impression of change in pain, and average daily steps. KEY RESULTS: The intervention did not produce statistically significant effects on the primary outcome (at 6 months, 32.4% of intervention participants had 30% improvement on the RMDQ vs. 24.7% of patients in usual care; aOR=1.61, 95% CI, 0.94 to 2.77), nor on other secondary outcomes assessed at 6 months, with the exception that intervention participants reported more favorable changes in pain relative to usual care (mean difference=-0.54, 95% CI, -0.85 to -0.23). Intervention participants also experienced a significant reduction in pain intensity and pain interference over 3 months (mean difference=-0.55, 95% CI, -0.88 to -0.22). CONCLUSIONS: A novel intervention to improve chronic pain among Black patients did not produce statistically significant improvements on the primary outcome relative to usual care. More intensive efforts are likely required among this population, many of whom were economically disadvantaged and had mental health comorbidities and physical limitations. TRIAL REGISTRATION: Clinicaltrials.gov Identifier: NCT01983228.