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Comparative Effectiveness of Online 8-session CBT vs. 1-Session Empowered Relief for Chronic Pain - The PROGRESS Study
RECRUITINGN/ASponsored by Stanford University
Actively Recruiting
PhaseN/A
SponsorStanford University
Started2023-01-01
Est. completion2029-05-01
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations5 sites
View on ClinicalTrials.gov →
NCT05612750
Summary
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).
Eligibility
Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria: 1. At least 18 years of age or older of either sex (and all genders). 2. Chronic pain (pain that occurs on at least half of the days of 3 months or more). 3. Past-month average pain intensity score of at least 3/10. 4. Ability to adhere to and complete study protocols. Exclusion Criteria: 1. Inability to provide informed consent. 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. Active suicidality at screening. 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. Receipt of either study treatment in the past 3 months.
Conditions3
LupusPain, ChronicPelvic Pain
Locations5 sites
Arizona
1 siteCalifornia
1 siteSCAN Health Plan
Long Beach, California, 90806
Kentucky
1 sitePennsylvania
1 siteLehigh Valley Health Network
Allentown, Pennsylvania, 18103
Elizabeth Heggan, BSelizabeth_a.heggan@lvhn.org
Utah
1 siteIntermountain Healthcare
Salt Lake City, Utah, 84103
Anne Haroldsen
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Actively Recruiting
PhaseN/A
SponsorStanford University
Started2023-01-01
Est. completion2029-05-01
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations5 sites
View on ClinicalTrials.gov →
NCT05612750