Comparative Effectiveness of Online 8-session CBT vs. 1-Session Empowered Relief for Chronic Pain - The PROGRESS Study
Sponsored by Stanford University
About this study
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).
The purpose of this study is to conduct a pragmatic clinical trial comparing the effectiveness: (1) 8-session cognitive behavioral therapy for chronic pain (pain-CBT); and (2) a 1-session pain relief skills intervention for chronic pain (Empowered Relief). The investigators aim to understand for patients which treatment works best. Online evidence-based behavioral treatment for pain will greatly expand access to patients across the U.S. living with diverse chronic pain conditions. Results from this study will fill several critical gaps in evidence that are preventing patients and physicians from making informed decisions about their pain care. This study will provide a low-cost, relatively low-risk, widely available and feasible protocol that directly addresses the needs of millions of c…
Where this study is enrolling (4)
- I'm interested
Phoenix VA Health Care System
Phoenix, Arizona
- I'm interested
SCAN Health Plan
Long Beach, California
- I'm interested
Humana
Louisville, Kentucky
- I'm interested
Lehigh Valley Health Network
Allentown, Pennsylvania
Who can participate
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 documented in medical records.
- ✕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.
Only the research team can confirm whether you qualify. The intake questionnaire is the best way to find out.
Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.
Trial data sourced from ClinicalTrials.gov.