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N/A N=44 Randomized Single-blind Treatment

Group-based Integrative Pain Management (IPMP+ Pilot)

Chronic Pain

Enrolled (actual)
44
Serious AEs
0.0%
Results posted
Jan 2025
Primary outcome: Primary: Percentage of Eligible Patients Who Are Randomized — 44 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
group acupuncture (Other); Integrative Group Medical Visits (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of California, San Francisco
Primary completion
Dec 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Eligible Patients Who Are Randomized
44
SECONDARY
Percentage of Randomized Participants Who Complete the Study
40
SECONDARY
Intervention Adherence
8.5; 5.5; 10.6

Summary

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 pilot 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.

Eligibility Criteria

Inclusion Criteria

  • adults aged > 18
  • fluency in English or Spanish;
  • panelled to a primary care provider at one of the study clinics;
  • diagnosis of chronic pain (> 3 months);
  • had a primary care visit for chronic pain within the past six months;
  • ability to provide a phone number;
  • able to participate in groups;
  • intent to be available for up to 24 weeks.

Exclusion Criteria

  • current anticoagulant use
  • active cancer treatment
  • inability to provide informed consent due to mental illness or cognitive impairment.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05906784). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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