[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100649964":3},{"organization":4,"armGroups":7,"interventions":34,"overallOfficials":12,"centralContacts":48,"locations":12,"responsibleParty":54,"collaborators":58,"id":62,"slug":63,"hasResults":64,"nctId":65,"briefTitle":66,"officialTitle":67,"acronym":68,"eligibilityCriteria":69,"healthyVolunteers":64,"sex":70,"minAge":71,"maxAge":12,"enrollmentInfo":72,"targetDuration":12,"studyType":75,"phases":76,"briefSummary":78,"conditions":79,"keywords":12,"overallStatus":82,"whyStopped":12,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":12},{"fullName":5,"class":6},"Henry Ford Health System","OTHER",[8,13,19,25,29],{"label":9,"type":10,"description":11,"interventionNames":12},"Subgroup 1","NO_INTERVENTION","Participants who were not randomized to the computerized brief intervention and were no longer on opioids 10 days post-baseline and did not receive any further treatment.",null,{"label":14,"type":15,"description":16,"interventionNames":17},"Subgroup 2","ACTIVE_COMPARATOR","Participants who were not randomized to the computerized brief intervention but were on opioids 10 days post-baseline and received recommendations for an opioid taper.",[18],"Behavioral: Opioid taper recommendations",{"label":20,"type":21,"description":22,"interventionNames":23},"Subgroup 3","EXPERIMENTAL","Participants who were randomized to the computerized brief intervention but were no longer on opioids 10 days post-baseline and did not receive any further treatment.",[24],"Behavioral: Computerized brief intervention",{"label":26,"type":21,"description":27,"interventionNames":28},"Subgroup 4","Participants who were randomized to the computerized brief intervention and were still on opioids 10 days post-baseline and were then randomized to receive the recommendations for the opioid taper.",[24,18],{"label":30,"type":21,"description":31,"interventionNames":32},"Subgroup 5","Participants who were randomized to the computerized brief intervention and were still on opioids 10 days post-baseline and were then randomized to receive the recommendations for the opioid taper plus additional psychological treatment sessions.",[24,33,18],"Behavioral: Psychological sessions",[35,40,44],{"type":36,"name":37,"description":38,"armGroupLabels":39,"otherNames":12},"BEHAVIORAL","Computerized brief intervention","Education about long-term opioid use and a mindfulness strategy",[20,26,30],{"type":36,"name":41,"description":42,"armGroupLabels":43,"otherNames":12},"Psychological sessions","Four sessions composed of education, mindfulness, and acceptance-based strategies.",[30],{"type":36,"name":45,"description":46,"armGroupLabels":47,"otherNames":12},"Opioid taper recommendations","Recommendations will be provided to taper opioid use.",[14,26,30],[49],{"name":50,"role":51,"phone":52,"phoneExt":12,"email":53},"Lisa Matero, PhD","CONTACT","313-874-5454","LMatero1@hfhs.org",{"type":55,"investigatorFullName":56,"investigatorTitle":57,"investigatorAffiliation":5,"oldNameTitle":12,"oldOrganization":12},"PRINCIPAL_INVESTIGATOR","Lisa Matero","Associate Scientist",[59],{"name":60,"class":61},"National Institute on Drug Abuse (NIDA)","NIH","100649964","healing-after-injury-to-reduce-opioid-use-and-pain-through-preventive-engagement-100649964",false,"NCT07741201","Healing After Injury to Reduce Opioid Use and Pain Through Preventive Engagement","An Adaptive Psychological Intervention to Improve Pain and Reduce Opioid Use Following an Injury","HOPE","Inclusion Criteria:\n\n* Admitted to Henry Ford Hospital\n* Has an acute musculoskeletal injury\n* Prescribed opioids during the admission\n\nExclusion Criteria:\n\n* Under age 18\n* Cognitive impairment (i.e., diagnosis of delirium, dementia, or traumatic brain injury\u002FGlasgow Coma Scale less than 13)\n* Chronic pain condition (i.e., pain most of the day, nearly every day for the past 3 months or longer)\n* Taking opioids 30 days or more prior to this hospitalization","ALL","18 Years",{"count":73,"type":74},80,"ESTIMATED","INTERVENTIONAL",[77],"NA","The goal of this proposed project is to optimize the adaptive psychological intervention and assess the feasibility and acceptability. The long-term objective of this line of research is to evaluate whether an adaptive psychological intervention delivered after a musculoskeletal injury is effective in preventing the development of chronic pain and long-term opioid use.",[80,81],"Pain","Opioid Use","NOT_YET_RECRUITING","2026-08-05",{"date":85,"type":86},"2026-08-10","ACTUAL",{"date":88,"type":74},"2027-03-01",{"date":90,"type":74},"2028-05-31",{"name":5,"class":6}]