Feasibility and Acceptability of Empowered Relief for American Indians With Pain During and After Cancer Treatment

NCT ID
NCT07742449
Registry status
Not yet recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
University of Oklahoma
Conditions
American Indian or Alaska Native, Cancer, Chronic Pain, Pain, Pain Management

Overview

ClinicalTrials.gov lists this study as Not yet recruiting.

Enrollment: 70 participants (Estimated).

What is being studied

  • Behavioral: Empowered Relief

Who may be eligible

Ages
18 Years to no maximum
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * Identifies as American Indian * Has history of a cancer diagnosis * Is currently undergoing or has completed active cancer treatment * Experiences body pain most or every day * Pain duration at least 3 months * English fluency Exclusion Criteria: * Significant psychological and cognitive impairment that limits one's ability to complete study tasks (completion of online survey, attending the Zoom-based ER class) * Life-threatening acute illness (e.g., infection, heart attack, injury) * No access to a computer, a smartphone, or a tablet

Study locations

1 study location is listed.

Site recruitment status is not specified in the registry data for these locations.

Countries: United States

  • Oklahoma, United States: 1

Sample of listed locations

  • Stephenson Cancer Center - Tulsa Location — Tulsa, Oklahoma, 74104, United States — Site recruitment status not specified in the registry data

Study details

Start date
October 1, 2026
Primary completion date
August 1, 2027
Completion date
December 1, 2027
First posted
August 3, 2026

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07742449
Registry last updated
September 18, 2026
QualifiedStudies registry data refreshed
September 28, 2026
QualifiedStudies record fetched
September 28, 2026

View NCT07742449 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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