RECRUITING

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

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

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.

Official Title

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

Quick Facts

Study Start:2025-04-15
Study Completion:2027-08-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06183281

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. 1. age 18 or older
  2. 2. speak English, Spanish, or Cantonese
  3. 3. have a UCSF Health or SFHN PCP
  4. 4. be willing to use a smartphone (iOS or Android - either their own or one provided by the study)
  5. 5. have chronic, non-malignant pain for at least 3 months
  6. 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
  1. * Severe mental illness or other condition preventing informed consent

Contacts and Locations

Study Contact

Jason Satterfield, PhD
CONTACT
415-353-2104
Jason.Satterfield@ucsf.edu

Principal Investigator

Jason Satterfield, PhD
PRINCIPAL_INVESTIGATOR
University of California, San Francisco

Study Locations (Sites)

San Francisco General Hospital
San Francisco, California, 94110
United States
UCSF Adult Primary Care Mt. Zion Clinic
San Francisco, California, 94115
United States

Collaborators and Investigators

Sponsor: University of California, San Francisco

  • Jason Satterfield, PhD, 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 Date2025-04-15
Study Completion Date2027-08-01

Study Record Updates

Study Start Date2025-04-15
Study Completion Date2027-08-01

Terms related to this study

Keywords Provided by Researchers

  • Non-malignant chronic pain
  • Digital health
  • Health coaching
  • Health equity
  • Cognitive therapy
  • Mindfulness
  • Movement

Additional Relevant MeSH Terms

  • Chronic Pain