[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100462821":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":18,"centralContacts":24,"locations":33,"responsibleParty":50,"collaborators":18,"id":54,"slug":18,"hasResults":55,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":55,"sex":61,"minAge":62,"maxAge":18,"enrollmentInfo":63,"targetDuration":18,"studyType":66,"phases":67,"briefSummary":69,"conditions":70,"keywords":77,"overallStatus":35,"whyStopped":18,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":92},{"fullName":5,"class":6},"Brigham and Women's Hospital","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"ACT intervention","EXPERIMENTAL","Participants assigned to this arm will complete a 1-day ACT workshop followed by a telephone booster after surgery",[13],"Behavioral: ACT intervention",{"label":15,"type":16,"description":17,"interventionNames":18},"Treatment As Usual","NO_INTERVENTION","Participants assigned to this arm will receive treatment as usual.",null,[20],{"type":21,"name":9,"description":22,"armGroupLabels":23,"otherNames":18},"BEHAVIORAL","One day in person workshop + telephone booster",[9],[25,30],{"name":26,"role":27,"phone":28,"phoneExt":18,"email":29},"Samantha M Meints, PhD","CONTACT","6177329014","smeints@bwh.harvard.edu",{"name":31,"role":27,"phone":18,"phoneExt":18,"email":32},"Marise Cornelius, MBA","mcornelius@bwh.harvard.edu",[34],{"facility":5,"status":35,"city":36,"state":37,"zip":38,"country":39,"countryCode":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"RECRUITING","Chestnut Hill","Massachusetts","01467","United States","US",{"type":42,"coordinates":43},"Point",[44,45],-71.16616,42.33065,{"lat":45,"lon":44},[48],{"name":49,"role":27,"phone":28,"phoneExt":18,"email":29},"Samantha M Meints",{"type":51,"investigatorFullName":52,"investigatorTitle":53,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"PRINCIPAL_INVESTIGATOR","Samantha Meints","Clinical Psychologist","100462821",false,"NCT05306665","PREventing Pain After Surgery","PREventing Pain After Surgery: a Feasibility and Acceptability Study of Acceptance and Commitment Therapy for the Prevention of Chronic Post-surgical Pain (PREPS)","PREPS","Inclusion Criteria:\n\n* scheduled to undergo fusion, discectomy, vertebroplasty, kyphoplasty, or foraminotomy\n* age 22 and older\n* able to communicate fluently in English\n\nExclusion Criteria:\n\n* inability to complete study procedures due to delirium, dementia, psychosis, or other cognitive impairment\n* have a history of severe neurologic movement disorder\n* are pregnant or intent to become pregnant during study\n* have undergone previous spinal surgery\n* have spinal deformity, pseudarthrosis, trauma, infection, or tumor as primary indication for surgery\n* have undergone Acceptance and Commitment Therapy in last 2 years","ALL","22 Years",{"count":64,"type":65},140,"ESTIMATED","INTERVENTIONAL",[68],"NA","The present study aims to adapt and modify a brief presurgical Acceptance and Commitment Therapy (ACT) intervention aimed at preventing the transition to Chronic Post-Surgical Pain (CPSP) and reducing long-term opioid use. Investigators will then assess the acceptability, feasibility, and preliminary efficacy of the finalized intervention to prevent the transition to CPSP and reduce post-surgical opioid use six months following lumbar spine surgery. Finally, investigators will identify psychosocial and psychophysical phenotypes associated with response to this intervention.",[71,72,73,74,75,76],"Pain, Back","Spinal Stenosis","Disc Herniation","Spondylosis","Spondylolisthesis","Back Injuries",[78,79,80,81,82],"Chronic pain","Surgery","opioid","acceptance and commitment therapy","Prevention","2024-10-25",{"date":85,"type":86},"2024-10-28","ACTUAL",{"date":88,"type":86},"2023-01-13",{"date":90,"type":65},"2026-08-01",{"name":5,"class":6},1]