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Recruiting NCT07578376

NCT07578376 Empowered Relief® for Cancer Survivors With Chronic Pain

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Clinical Trial Summary
NCT ID NCT07578376
Status Recruiting
Phase
Sponsor University of Oklahoma
Condition Chronic Pain Due to Cancer
Study Type INTERVENTIONAL
Enrollment 215 participants
Start Date 2026-06
Primary Completion 2029-12-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 120 Years
Study Type INTERVENTIONAL
Interventions
Empowered Relief Course (Zoom)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 215 participants in total. It began in 2026-06 with a primary completion date of 2029-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: History of cancer diagnosis, completion of active cancer treatment, cancer free at the time of enrollment, experience of body pain most or every day, pain duration at least 3 months, and 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), and no access to a computer, a smartphone or a tablet.

Contact & Investigator

Central Contact

Sophia You, PhD, ABPP

✉ Dokyoung-You@ou.edu

📞 918-660-3923

Principal Investigator

Sophia You, PhD, ABPP

PRINCIPAL INVESTIGATOR

University of Oklahoma

Frequently Asked Questions

Who can join the NCT07578376 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 120 Years, studying Chronic Pain Due to Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07578376 currently recruiting?

Yes, NCT07578376 is actively recruiting participants. Contact the research team at Dokyoung-You@ou.edu for enrollment information.

Where is the NCT07578376 trial being conducted?

This trial is being conducted at Tulsa, United States.

Who is sponsoring the NCT07578376 clinical trial?

NCT07578376 is sponsored by University of Oklahoma. The principal investigator is Sophia You, PhD, ABPP at University of Oklahoma. The trial plans to enroll 215 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology