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NCT05612750 · ClinicalTrials.gov registry record · NA
Comparative Effectiveness of Online 8-session CBT vs. 1-Session Empowered Relief for Chronic Pain - The PROGRESS Study
A NA study of Pain, Chronic and Pelvic Pain, sponsored by Stanford University.
- Recruiting
- Registry status
- NA
- Development phase
- 1,650
- Enrollment target
- 5
- Study locations
NCT05612750: Recruiting NA study of Pain, Chronic and Pelvic Pain, sponsored by Stanford University.
NCT05612750 is a NA study of Pain, Chronic and Pelvic Pain that is actively recruiting participants, run by Stanford University. The registered enrollment target is 1,650 participants, above the 687-participant average among 48 other Pain, Chronic trials with a reported enrollment target (140% higher). The trial reports 5 study locations across 5 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05612750, a NA study of Pain, Chronic and Pelvic Pain, is actively recruiting participants, sponsored by Stanford University.
- RECRUITING
- Registry status
- NA
- Development phase
- 1,650 participants
- Enrollment target
- 5
- Study locations
Study 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).
Primary Outcome
Compare study treatments for primary outcomes post-treatment with the Numeric Rating Scale (0-10)
Conditions Studied
Interventions
- BEHAVIORAL Cognitive Behavioral Therapy (CBT)
- BEHAVIORAL Empowered Relief
Study Locations (5)
Arizona
- Phoenix VA Health Care System - Phoenix
California
- SCAN Health Plan - Long Beach
Kentucky
- Humana - Louisville
Pennsylvania
- Lehigh Valley Health Network - Allentown
Utah
- Intermountain Healthcare - Salt Lake City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,650 participants |
| Start Date | 2023-01-01 |
| Est. Completion | 2029-05-01 |
| Phase | NA |
What NCT05612750 shows while recruiting
NCT05612750 is an interventional study that assigns participants to a tested intervention. Its 1,650 participants enrollment target places it among the larger protocols in the corpus, above the 687-participant average among 48 other Pain, Chronic trials with a reported enrollment target (140% higher).
The record links to 3 conditions, with Pain, Chronic appearing as the primary indexed condition, and to 2 interventions - of which Cognitive Behavioral Therapy (CBT) is the first listed.
NCT05612750 lists 5 locations in 5 states (Arizona, California, Kentucky).
Frequently Asked Questions
What is clinical trial NCT05612750 about?
NCT05612750 is a clinical study titled "Comparative Effectiveness of Online 8-session CBT vs. 1-Session Empowered Relief for Chronic Pain - The PROGRESS 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 hour...
What is the current status of trial NCT05612750?
This trial is currently recruiting. It is a NA study. The enrollment target is 1,650 participants. The study started on 2023-01-01. Estimated completion is 2029-05-01.
What conditions does trial NCT05612750 study?
This clinical trial studies the following conditions: Pain, Chronic, Pelvic Pain, Lupus.
What interventions are being tested in trial NCT05612750?
The interventions under investigation include: Cognitive Behavioral Therapy (CBT) (BEHAVIORAL), Empowered Relief (BEHAVIORAL).
Who is sponsoring clinical trial NCT05612750?
This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05612750 being conducted?
This trial has 5 study locations across Arizona, California, Kentucky, Pennsylvania, Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT05612750's enrollment target sits among peer trials
1,650 3rd of 48 higher than 46 of 48 other Pain, Chronic trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Pain, Chronic trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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