[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT07578376":3,"trial-entities:NCT07578376":95,"trial-summary:NCT07578376":99},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":7,"overall_status":8,"completion_date":9,"status_verified_date":10,"last_update_date":11,"start_date":12,"sponsor_name":13,"lead_sponsor_class":14,"has_dmc":15,"brief_summary":16,"detailed_description":17,"conditions":18,"keywords":21,"study_type":28,"primary_purpose":29,"phases":30,"enrollment_info":32,"interventions":35,"primary_outcomes":41,"secondary_outcomes":46,"sex":58,"minimum_age":59,"maximum_age":60,"healthy_volunteers":61,"eligibility_criteria":62,"std_ages":66,"locations":69,"central_contacts":84,"overall_officials":90,"references":93,"see_also_links":94},"NCT07578376","18957P","Empowered Relief® for Cancer Survivors With Chronic Pain","Feasibility and Preliminary Efficacy of Empowered Relief® for Cancer Survivors With Chronic Pain","RECRUITING","2030-04-30","2026-05","2026-05-14","2026-06","University of Oklahoma","OTHER",true,"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.","The Empowered Relief (ER) study is a Zoom-based, 1-session, 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 use and supportive daily text messages. Participants will fill out a series of follow-up surveys at the 1, 2, and 3-month post-class mark. These surveys will be directly compared to surveys given to participants that do not complete the course. Class admittance will be randomized, however, participants not in the treatment group will have the option to take the course after the 3-month observatory period. 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. Because of its brief, didactic nature and delivery via Zoom, ER can accommodate large class sizes and may address access disparities among underserved cancer survivors. ER is currently 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. Yet, Empowered Relief has not been tested in cancer survivors.",[19,20],"Chronic Pain Due to Cancer","Pain Catastrophizing",[22,23,24,25,26,27],"Empowered Relief","Chronic Pain","Cancer survivor","Survey Study","Monthly follow-ups","Zoom class","INTERVENTIONAL","TREATMENT",[31],"NA",{"count":33,"type":34},215,"ESTIMATED",[36],{"type":37,"name":38,"description":39,"armGroupLabels":40},"BEHAVIORAL","Empowered Relief Course (Zoom)","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.",[22],[42],{"measure":43,"description":44,"timeFrame":45},"Overall treatment satisfaction","0-10 scale, higher scores indicate greater satisfaction, mean should be 8 or higher","Immediately after intervention",[47,51,54,57],{"measure":48,"description":49,"timeFrame":50},"Pain Intensity","0-10 scale, higher scores indicate higher pain","1 month after intervention",{"measure":52,"description":53,"timeFrame":50},"Pain Interference","T-scores, higher scores indicate higher pain interference",{"measure":48,"description":55,"timeFrame":56},"0-10 Scale, higher scores indicate higher pain","3 months after intervention",{"measure":52,"description":53,"timeFrame":56},"ALL","18 Years","120 Years",false,{"inclusion":63,"exclusion":64,"raw_text":65},[],[],"Inclusion Criteria:\n\nHistory 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.\n\nExclusion Criteria:\n\nSignificant 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.",[67,68],"ADULT","OLDER_ADULT",[70],{"facility":71,"status":8,"city":72,"state":73,"zip":74,"country":75,"contacts":76,"geoPoint":81},"University of Oklahoma Schusterman Center - Tulsa","Tulsa","Oklahoma","74135","United States",[77],{"name":78,"role":79,"email":80},"Jordan Keast, BS","CONTACT","jordan-keast@ou.edu",{"lat":82,"lon":83},36.15398,-95.99277,[85,89],{"name":86,"role":79,"phone":87,"email":88},"Sophia You, PhD, ABPP","918-660-3923","Dokyoung-You@ou.edu",{"name":78,"role":79,"email":80},[91],{"name":86,"affiliation":13,"role":92},"PRINCIPAL_INVESTIGATOR",[],[],{"nct_id":4,"conditions":96,"biomarkers":98},[23,97],"Malignant Neoplasm",[],{"nct_id":4,"found":15,"summary":100,"prompt_version":109},{"design":101,"status":102,"heading":6,"summary":103,"follow_up":104,"word_count":105,"commitments":106,"compensation":107,"drugs_mentioned":108},"This is a randomized controlled study, meaning participants will be randomly assigned to either take the Empowered Relief class or be on a waitlist. The study plans to enroll 215 participants.","completed","This study is testing a program called Empowered Relief® for cancer survivors who have chronic pain. Empowered Relief® is a one-time, two-hour online class that teaches skills to manage pain. You will learn three core pain relief skills, create a personal plan, and get access to a special audio app and daily text messages. We want to see how satisfied people are with this program right after they take it. You can join if you are 18 to 120 years old, have finished cancer treatment, are cancer-free now, have body pain most days for at least three months, and speak English. The study is currently unclear on its recruitment status, but aims to enroll 215 people.","Participants will be followed for three months after the class, completing surveys at 1, 2, and 3 months.",116,"Participants will attend a one-time, two-hour online class. You will also complete follow-up surveys at 1, 2, and 3 months after the class.","Not stated in the trial record.",[],"v2"]