RECRUITING

Integrating Nonpharmacologic Strategies for Pain With Inclusion, Respect, and Equity

Description

INSPIRE creates a trilingual mobile app and telehealth coaching program to promote non-pharmacologic strategies for pain management with Black, Chinese, and Latinx communities in the San Francisco Bay Area. Years 1-2 will develop the app and test it with a brief single arm pilot starting in Nov 2023. A full two arm randomized controlled trial (RCT) will being in early 2025 with changes in PEG scores as the primary outcome. Secondary outcomes include Helping to End Addiction Longterm (HEAL) common data elements.

Conditions

Study Overview

Study Details

Study overview

INSPIRE creates a trilingual mobile app and telehealth coaching program to promote non-pharmacologic strategies for pain management with Black, Chinese, and Latinx communities in the San Francisco Bay Area. Years 1-2 will develop the app and test it with a brief single arm pilot starting in Nov 2023. A full two arm randomized controlled trial (RCT) will being in early 2025 with changes in PEG scores as the primary outcome. Secondary outcomes include Helping to End Addiction Longterm (HEAL) common data elements.

Integrating Nonpharmacologic Strategies for Pain With Inclusion, Respect, and Equity (INSPIRE): Tailored Digital Tools, Telehealth Coaching, and Primary Care Coordination

Integrating Nonpharmacologic Strategies for Pain With Inclusion, Respect, and Equity

Condition
Chronic Pain
Intervention / Treatment

-

Contacts and Locations

San Francisco

San Francisco General Hospital, San Francisco, California, United States, 94110

San Francisco

UCSF Adult Primary Care Mt. Zion Clinic, San Francisco, California, United States, 94115

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. age 18 or older
  • 2. speak English, Spanish, or Cantonese
  • 3. have a UCSF Health or SFHN PCP
  • 4. be willing to use a smartphone (iOS or Android - either their own or one provided by the study)
  • 5. have chronic, non-malignant pain for at least 3 months
  • 6. be willing to participate in a 12 month patient-centered chronic pain management study where they will be randomized into one of two comparison arms
  • * Severe mental illness or other condition preventing informed consent

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of California, San Francisco,

Jason Satterfield, PhD, PRINCIPAL_INVESTIGATOR, University of California, San Francisco

Study Record Dates

2027-08-01