RECRUITING

Comparative Effectiveness of Online 8-session CBT Vs. 1-Session Empowered Relief for Chronic Pain - the PROGRESS Study

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

The purpose of this study is to conduct a pragmatic clinical trial comparing the effectiveness of: (1) 8-week cognitive behavioral therapy for chronic pain (pain-CBT; sixteen hours total treatment time); and (2) a 1-session pain relief skills intervention for chronic pain (Empowered Relief; two hours total treatment time).

Official Title

Comparative Effectiveness of Online Cognitive Behavioral Therapy Vs. an Online Single-Session Pain Relief Skills Class for Chronic Pain - the PROGRESS Study

Quick Facts

Study Start:2023-01-01
Study Completion:2029-05-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05612750

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. At least 18 years of age or older of either sex (and all genders).
  2. 2. Chronic pain (pain that occurs on at least half of the days of 3 months or more).
  3. 3. Past-month average pain intensity score of at least 3/10.
  4. 4. Ability to adhere to and complete study protocols.
  1. 1. Inability to provide informed consent.
  2. 2. Cognitive impairment, non-English speaking, or psychological factors that would preclude comprehension of material and/or full participation in the study including group treatment.
  3. 3. Active suicidality at screening.
  4. 4. Study staff may exclude individuals with a known history of disruptive behavior to minimize contamination of the learning environment for an entire treatment cohort.
  5. 5. Receipt of either study treatment in the past 3 months.

Contacts and Locations

Study Contact

Emma A Adair, BS
CONTACT
6097448937
eadair@stanford.edu
Corinne Jung, PhD
CONTACT
(650) 724-0522
Cejung@stanford.edu

Study Locations (Sites)

Phoenix VA Health Care System
Phoenix, Arizona, 85012
United States
SCAN Health Plan
Long Beach, California, 90806
United States
Humana
Louisville, Kentucky, 40202
United States
Lehigh Valley Health Network
Allentown, Pennsylvania, 18103
United States
Intermountain Healthcare
Salt Lake City, Utah, 84103
United States

Collaborators and Investigators

Sponsor: Stanford University

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 Date2023-01-01
Study Completion Date2029-05-01

Study Record Updates

Study Start Date2023-01-01
Study Completion Date2029-05-01

Terms related to this study

Keywords Provided by Researchers

  • Young adult
  • Lupus
  • Pelvic Pain
  • Behavioral Health

Additional Relevant MeSH Terms

  • Pain, Chronic
  • Lupus
  • Pelvic Pain