Actively Recruiting
Group-based Integrative Pain Management in Primary Care Safety Net Clinics
Led by University of California, San Francisco · Updated on 2026-01-26
360
Participants Needed
1
Research Sites
146 weeks
Total Duration
On this page
Sponsors
U
University of California, San Francisco
Lead Sponsor
N
National Institute on Minority Health and Health Disparities (NIMHD)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Socioeconomically disadvantaged populations have a high prevalence of chronic pain, exacerbated by social isolation, intersectional stigma, and disparities in pain assessment and treatment options. Effective interventions using a multilevel, biopsychosocial approach are needed to decrease the unequal burden of pain. The proposed study will test group-based integrative models of pain management in primary care safety net clinics to improve pain care for racially and ethnically diverse low-income patients.
CONDITIONS
Official Title
Group-based Integrative Pain Management in Primary Care Safety Net Clinics
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 60; 18
- Fluent in English or Spanish
- Assigned to a primary care provider at one of the study clinics
- Diagnosed with chronic pain lasting more than 3 months
- Had a primary care visit for chronic pain within the past 6 months
- Able to provide a phone number
- Able to participate in group sessions
- Intend to be available for up to 24 weeks
You will not qualify if you...
- Received group-based pain management in the past 3 months
- Received acupuncture treatment for pain in the past 3 months
- Currently receiving active cancer treatment
- Unable to provide informed consent due to mental illness or cognitive impairment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Tom Waddell Urban Health Clinic
San Francisco, California, United States, 94102
Actively Recruiting
Research Team
J
Julia Wu, MPH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
FACTORIAL
Primary Purpose
TREATMENT
Number of Arms
4
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