[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"chronic-pain-management\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:chronic-pain-management":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,44,73,102],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100639082","using-virtual-reality-applications-for-younger-patients-with-chronic-pain-100639082",false,"NCT07630350","Using Virtual Reality Applications for Younger Patients With Chronic Pain","Use of Virtual Reality in Outpatient Management of Pediatric Chronic Pain of Head, Neck and Upper Extremity","Inclusion Criteria:\n\n* Patients 7-21 years of age\n* Patients who have been evaluated in the pediatric chronic pain clinic during the enrollment period or last 12 months\n* Patients who have a diagnosis of migraine, chronic neck pain, chronic shoulder or scapular pain, chronic pain of the upper limb, complex regional pain syndrome of the upper limb, amplified musculoskeletal pain syndrome affecting the upper limb, chronic joint pain affecting the upper limb\n\nExclusion Criteria:\n\n* Patients less than 7 years or greater than 21 years of age\n* Patients who have not been evaluated in the pediatric chronic pain clinic during the enrollment period or last 12 months.\n* Patients with primary complaints of lower back pain, hip pain, knee pain, ankle pain, or abdominal pain.\n* Patients with factors limit their ability to safely tolerate wearing and operating the Meta Oculus 2 virtual reality goggles, including but not limited to claustrophobia, anxiety, vestibulo-ocular dysfunction, visual impairments, significant sitting balance impairments.","ALL","7 Years","21 Years",{"count":20,"type":21},20,"ESTIMATED","INTERVENTIONAL",[24],"NA","In this study, patients who are 7-21 years of age and have chronic pain affecting their head, neck, and\u002For upper limb will participate in 6 once-weekly sessions. During each of these hour-long sessions, participants will engage in physical therapy exercises, use virtual reality games focused on moving the head, neck and arm, and complete questionnaires about their pain.",[27],"Chronic Pain Management",[29,30],"pediatric","virtual reality","NOT_YET_RECRUITING","2026-06-01",{"date":34,"type":35},"2026-06-05","ACTUAL",{"date":37,"type":21},"2026-06",{"date":39,"type":21},"2027-03",{"name":41,"class":42},"Elizabeth Pickle","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":22,"phases":56,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":61,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":72},"100581932","improved-treatment-for-patients-with-long-term-opioid-therapy-for-non-cancer-pain-in-primary-care-100581932","NCT06856733","Improved Treatment for Patients With Long-term Opioid Therapy for Non-cancer Pain in Primary Care","Improved Treatment for Patients With Long-term Opioid Therapy for Non-cancer Pain in Primary Care (Opi-Prim)","Opi-Prim","Inclusion Criteria:\n\n* Having received the equivalent of 90 days or more prescription of opioids for chronic pain made by the general practitioner during the recent 12 months\n* Able to speak Swedish or English\n\nExclusion Criteria:\n\n* Having been referred to a pain clinic (either at hospital or multimodal rehabilitation in primary care) within the last 6 months\n* No current opioid use, severe cognitive dysfunction, e.g., suicidal ideation, psychotic symptoms, or dementia, that prevents informed consent.\n* Using their opioids for cancer pain","18 Years","70 Years",{"count":55,"type":21},110,[24],"The goal of this clinical trial is to reduce inappropriate long term opioid treatment (LTOT) and to optimize pain management in patients with LTOT for chronic non-cancer pain in primary care through a new person-centred and team-based approach. The main question it aims to answer is:\n\nWhat are the effects of a new person-centred and team-based approach on pain interference in patients with LTOT for chronic non-cancer pain in primary care?\n\nResearchers will compare a new person-centred and team-based approach to usual care to see if pain interference is lower.\n\nParticipants will receive a person-centred team-based treatment consisting of:\n\n* Phase 1 (investigation and assessment, week 1-3): A medication review, pain analysis and other assessments through separate visits to a pharmacist, general practitioner, physiotherapist, psychologist and care manager\n* Phase 2 (treatment plan, week 3-4): A team consultations with all healthcare personnel involved in Phase 1 including the patient where an individualized rehabilitation plan is made based.\n* Phase 3 (treatment and follow-up, week 4-24): Implementation of the individualized rehabilitation plan with frequent follow-up contacts (1 per 1-3 weeks) by phone with the care manager.",[59,27,60],"Chronic Pain","Primary Care","RECRUITING","2026-05-08",{"date":64,"type":35},"2026-05-13",{"date":66,"type":35},"2025-03-10",{"date":68,"type":21},"2029-06-30",{"name":70,"class":71},"Uppsala County Council, Sweden","OTHER_GOV",3,{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":4,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":16,"minAge":80,"maxAge":4,"enrollmentInfo":81,"targetDuration":4,"studyType":22,"phases":83,"briefSummary":85,"conditions":86,"keywords":88,"overallStatus":61,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":72},"100587784","phase-3-the-beat-pain-better-trial-100587784","NCT06932887","The Beat Pain Better Trial","Mountain West Arthritis Secondary Prevention Program - The Beat Pain Better Trial","Inclusion Criteria:\n\n1. Age 45 or older;\n2. Visit in participating medical clinic within the past 6 months\n3. OA diagnosis code related to lower extremity and\u002For spine on the problem list or associ¬ated with an encounter in the past 6 months\n4. Has functioning cell phone able to receive calls and texts\n\nExclusion Criteria:\n\n1. Unable to participate in a regular walking program defined as the ability to walk for at least five minutes with or without the use of an assistive device.\n2. Medical contraindication to participation in physical activity\n3. Unable to communicate in either Spanish or English","45 Years",{"count":82,"type":21},346,[84],"PHASE3","The Beat Pain Better study examines strategies to increase the reach of evidence-based interventions for persons with osteoarthritis (OA) in communities that experience disparities. The study is a hybrid type 3 effectiveness-imple-mentation trial using sequential, multiple assignment, ran¬domi¬zation to evaluate 1) two text mes¬saging strat¬egies to reach persons with OA and enroll them in physical activity counseling provided by physical therapists; and 2) two strat¬egies to engage enrolled persons in the Walk with Ease (WWE) intervention for sustained self-management.",[87,27],"Osteoarthritis",[89,90,91,92],"osteoarthritis","chronic pain","physical therapy","self-management","2026-01-27",{"date":95,"type":35},"2026-01-29",{"date":97,"type":35},"2025-05-28",{"date":99,"type":21},"2028-03-31",{"name":101,"class":42},"University of Utah",{"id":103,"slug":104,"hasResults":11,"nctId":105,"briefTitle":106,"officialTitle":107,"acronym":4,"eligibilityCriteria":108,"healthyVolunteers":11,"sex":16,"minAge":52,"maxAge":109,"enrollmentInfo":110,"targetDuration":4,"studyType":22,"phases":112,"briefSummary":113,"conditions":114,"keywords":118,"overallStatus":61,"whyStopped":4,"lastUpdateSubmitDate":123,"lastUpdatePostDateStruct":124,"startDateStruct":126,"completionDateStruct":128,"leadSponsor":130,"locationsCount":72},"100606704","evaluating-the-auricular-point-acupressure-self-management-program-for-chronic-musculoskeletal-pain-among-rural-populations-100606704","NCT07179016","Evaluating the Auricular Point Acupressure-Self Management Program for Chronic Musculoskeletal Pain Among Rural Populations","A Pragmatic, Randomized Controlled Trial of a Auricular Point Acupressure - Self-Management (APA-SM) Program for Chronic Musculoskeletal Pain Among Rural Populations.","Inclusion Criteria:\n\n* Receive any pain management for CMP (neck, back, shoulder, hands, hips, knees, feet)\n* Have CMP ≥ 4 on a scale of 0-10 that has persisted for at least 3 months or has resulted in pain on at least half the days in the past 6 months\n\nExclusion Criteria:\n\n* Severe ear skin disorder (Diagnosed with conditions e.g., eczema, lupus with skin involvement) which often require medical intervention and severe allergy to tape\n* Inability or unwillingness to provide informed consent\n* Use of some type of hearing aid where size may obstruct seed placement\n* Not living in rural area","85 Years",{"count":111,"type":21},693,[24],"The investigators will test an Auricular Point Acupressure Self-Management (APA-SM) program integrated into rural primary and specialty care and rural communities for chronic musculoskeletal pain (CMP). To maximize self-management of pain, the investigators developed a smartphone app which will allow the participants to learn to self-administer APA. The investigators will have 3 arms (APA-SM self-guided with remote training, APA-SM with in-person training, and Education Control) with 231 participants per arm (total=693 for 3 arms). The investigators will evaluate the clinical effectiveness of our 4-week APA-SM intervention compared to control in primary outcomes (pain intensity, pain interference, activity), secondary outcomes (HEAL Clinical Pain Core common data elements), and analgesic use up to 6 months follow-up.",[115,27,116,117],"Chronic Pain (Back \u002F Neck)","Chronic Knee Pain","Joint Pain",[59,119,120,121,122],"Rural population","Self-management","Chronic musculoskeletal pain","Auricular point acupressure","2025-09-24",{"date":125,"type":35},"2025-10-01",{"date":127,"type":35},"2025-09-11",{"date":129,"type":21},"2029-08-31",{"name":131,"class":42},"The University of Texas Health Science Center, Houston"]