Tele-Collaborative Outreach to Rural Patients With Chronic Pain
Tele-Collaborative Outreach to Rural Patients With Chronic Pain: The CORPs Trial
Oregon Health and Science University
608 participants
Jul 11, 2024
INTERVENTIONAL
Conditions
Summary
This is a randomized controlled trial comparing the effectiveness of a remotely delivered collaborative care intervention for chronic pain versus a minimally enhanced control group. The specific aims of the study are: (1) compare the effectiveness of tele-collaborative pain care vs. minimally enhanced usual care to improve pain interference over 12 months of follow-up, and (2) oversample women and rural veterans of minoritized race/ethnicity to test heterogeneity of treatment effects across birth sex and race/ethnicity.
Eligibility
Inclusion Criteria5
- U.S. Veteran
- Rural Residence based on Rural Urban Commuting Area codes
- High Impact Chronic pain, determined through a phone screening
- Access to landline or cell phone
- English Speaking
Exclusion Criteria6
- Cognitive impairment that would impact participation in the study
- Plans to move in the next 3 months
- Surgery in the past 3 months
- In long-term inpatient or hospice care
- Terminal illness (defined as life expectancy of less than 12 months)
- Active participation in another pain intervention study
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Interventions
Participants will be randomly assigned to the intervention or to the comparator arm. The follow-up period is 12 months. The primary outcome is a change in pain interference. After the baseline assessment, participants will complete a masked telephone assessments with research staff at 3-, 6-, 9-, and 12-months. A subset of individuals may be invited to participate in a qualitative interview at 12-month follow-up.
Participants will be randomly assigned to the intervention or to the comparator arm. The follow-up period is 12 months. The primary outcome is a change in pain interference. After the baseline assessment, participants will complete a masked telephone assessments with research staff at 3-, 6-, 9-, and 12-months. A subset of individuals may be invited to participate in a qualitative interview at 12-month follow-up.
Locations(4)
View Full Details on ClinicalTrials.gov
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NCT06091202