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

NCT07742449 — Not applicable, Not yet recruiting, 70 participants, University of Oklahoma

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RegistryNCT07742449, acronym ejames3
StatusNot yet recruiting
PhaseNot applicable
Study typeInterventional; na, single group, masking: none, supportive care
Enrollment70 (Estimated)
SponsorUniversity of Oklahoma (Other)
ConditionsCancer, Pain, Pain Management, Chronic Pain, American Indian or Alaska Native
InterventionsEmpowered Relief (Behavioral)
Datesstart 2026-10-01 (estimated), primary completion 2027-08-01 (estimated), completion 2027-12-01 (estimated), first posted 2026-08-03, last updated 2026-09-18
Locations1 site in United States

Related Papers Related Patents Related Grants Related Experts
All trials for Cancer All trials for Pain All trials of Empowered Relief

-Summary

This project will evaluate the feasibility and acceptability of Empowered Relief (ER) among American Indian adults who are currently receiving or have completed active cancer treatments at Stephenson Cancer Center (SCC). ER is a single-session, Zoom-based, 2-hour, 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 practice. ER has demonstrated moderate efficacy in individuals with chronic non-cancer pain, reducing pain intensity, pain interference, pain-related distress (pain catastrophizing), sleep disturbance, and anxiety at 3 and 6 months post-treatment. Because of its brief, didactic nature and Zoom delivery, ER can accommodate large class sizes and may address accessibility disparities among underserved cancer populations. While ER is being studied across various non-cancer populations and has been adopted as standard of care in leading healthcare institutions in the U.S. and abroad, it has not been tested in American Indians with cancer.

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+Arms and interventions

ArmTypeInterventionsDescription
Empowered ReliefExperimentalBehavioral: Empowered ReliefParticipants in this arm will complete a 2-hour Empowered Relief pain management course and get access to all the course materials. Participants will complete a series of follow-up surveys assessing the feasibility of the class for their pain intervention.
  • Empowered Relief (Behavioral): ER is a single-session, Zoom-based, 2-hour, 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 practice. ER has demonstrated moderate efficacy in individuals with chronic non-cancer pain, reducing pain intensity, pain interference, pain-related distress (pain catastrophizing), sleep disturbance, and anxiety at 3 and 6 months post-treatment.

+Outcome measures

Primary outcomes

  • Feasibility of ER in American Indian populations [From participant accrual to the completion of their 3-mon follow up survey (approx. 4 months)]: Indexed by: * ≥70% attendance rate amongst all eligible participants * An average treatment satisfaction rating of ≥ 8 on a 0-10 scale (with 0 being completely dissatisfied and 10 being completely satisfied) * Successful recruitment and completion of 70 participants within one year Measures will be factored together to make an assessment on total feasibility.
  • Identify areas for cultural tailoring and improvement of ER [Assessed as part of the optional (n=30) Qualitative Post-class interview. (approx. 30 minutes)]: We will use qualitative data from interviews to generate actionable recommendations to improve the cultural engagement, acceptability, and relevance of ER for American Indians with cancer.
  • Pain Intensity [Data collected at the 1-, 2-, and 3-month follow up survey following the ER class]: Pain intensity will be reported on a scale from 1-10, with 1 being "No Pain" and 10 being "Worst Pain Imaginable."
  • Pain Interference [Data collected at the 1-, 2-, and 3-month follow up survey following the ER class.]: Pain interference will be gauged using a series of questions decerning the impact of the participants participants pain on daily activities. Participants will rate the interference on a scale from 1-5, with 1 being "Not at All" and 5 being "Very Much."
  • Emotional Distress [Data collected at the 1-, 2-, and 3-month follow up survey following the ER class.]: Emotional distress will be measured using a series of questionnaires asking participants about the frequency of certain emotional reactions. Participants will report frequency on a scale from 1-5, with 1 being "Never" and 5 being "Always."
  • Sleep Disturbance [Data collected at the 1-, 2-, and 3-month follow up survey following the ER class.]: Sleep Disturbance will be recorded using a series of questions rating the quality and frequency of sleep. Participants will report on quality and frequency on a scale from 1-5, with 1 being "Very Poor/Not at All" and 5 being "Very Good/Very Much."
  • Perceived Quality of Life [Data collected at the 1-, 2-, and 3-month follow up survey following the ER class.]: Perceived Quality of Life will be reported on a scale from 1-5, with 1 being "Poor" and 5 being "Excellent."

+Eligibility

Sex: All, ages: 18 Years to any

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

+Locations (1)

FacilityCityCountryStatus
Stephenson Cancer Center - Tulsa LocationTulsa, OklahomaUnited States

+Investigators

  • Sophia You, Principal investigator, University of Oklahoma