RECRUITING

Group-based Integrative Pain Management in Primary Care Safety Net Clinics

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Group-based Integrative Pain Management: A Multi-level Approach to Address Intersectional Stigma and Social Isolation in Diverse Primary Care Safety Net Patients With Chronic Pain

Quick Facts

Study Start:2024-07-12
Study Completion:2027-04-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06327542

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adults aged ≥ 18
  2. * Fluency in English or Spanish
  3. * Panelled to a primary care provider at one of the study clinics
  4. * Diagnosis of chronic pain (\> 3 months)
  5. * Had a primary care visit for chronic pain within the past six months
  6. * Ability to provide a phone number
  7. * Able to participate in groups
  8. * Intent to be available for up to 24 weeks
  1. * Received group-based pain management in the past 3 months
  2. * Received acupuncture treatment for pain in the past 3 months
  3. * Active cancer treatment
  4. * Inability to provide informed consent due to mental illness or cognitive impairment

Contacts and Locations

Study Contact

Julia Wu, MPH
CONTACT
415-502-8733
Julia.Wu@ucsf.edu

Principal Investigator

Maria Chao, DrPH, MPA
PRINCIPAL_INVESTIGATOR
University of California, San Francisco

Study Locations (Sites)

Tom Waddell Urban Health Clinic
San Francisco, California, 94102
United States

Collaborators and Investigators

Sponsor: University of California, San Francisco

  • Maria Chao, DrPH, MPA, PRINCIPAL_INVESTIGATOR, University of California, San Francisco

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-07-12
Study Completion Date2027-04-30

Study Record Updates

Study Start Date2024-07-12
Study Completion Date2027-04-30

Terms related to this study

Keywords Provided by Researchers

  • health equity
  • integrative health
  • nonpharmacologic pain management
  • stigma
  • social isolation
  • primary care
  • group medical visits

Additional Relevant MeSH Terms

  • Chronic Pain