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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 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.
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).
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 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05612750
The ClinicalTrials.gov registry entry for NCT05612750 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 1,650 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 687-participant average among 48 other Pain, Chronic trials with a reported enrollment target (140% higher). The listed sponsor is Stanford University, which has 1,744 total studies on file at ClinicalTrials.gov.
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 reports 5 study locations spanning 5 distinct geographic areas - top geographies include 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.
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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.