Empowered Relief® for Cancer Survivors With Chronic Pain

Part of paid clinical trials in Tulsa, Oklahoma.

Sponsor
University of Oklahoma
Study ID
NCT07578376
Status
Recruiting
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Conditions

  • Chronic Pain Due to Cancer
  • Pain Catastrophizing

Eligibility Criteria

Sex
ALL
Age
18 Years - 120 Years
Healthy Volunteers
Not accepted

Interventions

  • Empowered Relief Course (Zoom) — BEHAVIORAL
    This is a one-time 2 hour long skills-based pain management class delivered by certified instructors. Participants learn three core pain relief skills, develop a personalized plan, and receive access to a free binaural audio app for daily use and supportive daily text messages.

Study Details

This randomized controlled study to examine the efficacy of ER class in cancer survivors with chronic pain. Eligible participants will be randomly assigned to a ER class or a waitlist control condition. We will recruit 250 participants with a goal of having 200 completers (20% attrition). Participants in the control condition will be invited to attend ER class after the 3-month observation period.

Key Dates

Start date
Jun 30, 2026
Status verified
May 2026
Primary completion
Dec 31, 2029
Completion
Apr 30, 2030

Study Design

Enrollment
215 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Empowered Relief
    Participants in this arm of the study will complete the one-time 2hr Empowered Relief zoom course. They will also complete a post-course survey as well as the standardized 1, 2, and 3-month follow-up surveys.
  • No Intervention: Wait-List Control
    Participants in the Wait-List Control (WLC) arm will not have initial access to the empowered relief course. Additionally they will not have to complete a post-course survey. The WLC group will be asked to complete the 1, 2, and 3-month follow-up studies after no intervention. After this 3-month observatory period, WLC participants will have voluntary access to the Empowered Relief course.

Primary Outcome Measure

Overall treatment satisfaction [ Time Frame: Immediately after intervention ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of Oklahoma Schusterman Center - TulsaTulsaOklahoma74135
Jordan Keast, BS
[email protected]

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By research site
University of Oklahoma Schusterman Center - Tulsa· Tulsa, OK

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