[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100651509":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":25,"centralContacts":29,"locations":35,"responsibleParty":56,"collaborators":60,"id":63,"slug":64,"hasResults":65,"nctId":66,"briefTitle":67,"officialTitle":68,"acronym":69,"eligibilityCriteria":70,"healthyVolunteers":65,"sex":71,"minAge":72,"maxAge":25,"enrollmentInfo":73,"targetDuration":25,"studyType":76,"phases":77,"briefSummary":79,"conditions":80,"keywords":82,"overallStatus":86,"whyStopped":25,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":96},{"fullName":5,"class":6},"University of Delaware","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Strong but Comfortable TENS","EXPERIMENTAL","Participants in this group will received 'strong but comfortable' intensity transcutaneous electrical stimulation (TENS) for up to 10 treatment sessions over 2 weeks.",[13],"Device: Strong But Comfortable TENS",{"label":15,"type":10,"description":16,"interventionNames":17},"Just Perceptible TENS","Participants in this group will receive 'just perceptible' intensity transcutaneous electrical stimulation (TENS) for up to 10 treatment sessions over 2 weeks.",[18],"Device: Just Perceptible TENS",[20,26],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"DEVICE","Strong But Comfortable TENS","All pads of the electrical stimulation suit will be turned on to an intensity that is perceived as 'strong but comfortable', but without a muscle contraction. Transcutaneous electrical stimulation (TENS) intensities will be recorded each visit and determined at each treatment session, without referencing prior stimulation intensities. TENS will be applied for 40 minutes.",[9],null,{"type":21,"name":15,"description":27,"armGroupLabels":28,"otherNames":25},"All pads of the electrical stimulation suit will be turned on to a 'just perceptible' intensity. Transcutaneous electrical stimulation (TENS) intensities will be recorded each visit and determined at each treatment session, without referencing prior stimulation intensities. TENS will be applied for 40 minutes.",[15],[30],{"name":31,"role":32,"phone":33,"phoneExt":25,"email":34},"J. Megan Sions, PT, DPT, PhD","CONTACT","302-831-7231","megsions@udel.edu",[36],{"facility":37,"status":25,"city":38,"state":39,"zip":40,"country":41,"countryCode":42,"cosmosGeoPoint":43,"geoPoint":48,"contacts":49},"International Institute of Orthotics and Prosthetics","Tampa","Florida","33634","United States","US",{"type":44,"coordinates":45},"Point",[46,47],-82.45843,27.94752,{"lat":47,"lon":46},[50,53],{"name":51,"role":32,"phone":52,"phoneExt":25,"email":25},"Arlene Gillis","813-517-1740",{"name":54,"role":55,"phone":25,"phoneExt":25,"email":25},"Michael Hoggatt, PT, DPT, MSPO","SUB_INVESTIGATOR",{"type":57,"investigatorFullName":58,"investigatorTitle":59,"investigatorAffiliation":5,"oldNameTitle":25,"oldOrganization":25},"PRINCIPAL_INVESTIGATOR","Jaclyn Sions","Associate Professor",[61],{"name":37,"class":62},"UNKNOWN","100651509","stimulation-for-amputation-pain-management-100651509",false,"NCT07759219","Stimulation for Amputation Pain Management","STAMP Study: Stimulation for Amputation Pain Management","STAMP","Inclusion Criteria:\n\n* English-speaking and reading to enable informed consent and participation\n* Report of pain in 2\u002Fmore body regions for at least 3 months duration per site • Report of at least moderate intensity pain over the past 7 days\n\nExclusion Criteria:\n\n* An amputation of the contralateral lower-limb \\> toe-level\n* Do not currently use a prosthesis to ambulate\n* Diagnosed cognitive impairment (e.g., dementia, traumatic brain injury)\n* Severe vision (e.g., blind) or hearing loss (e.g., deaf)\n* Are currently pregnant\n* Active cancer\u002Fmalignancy\n* Open wound in any area that is covered by the suit\n* An acute infection or injury (e.g., fracture)\n* Deep vein thrombosis\n* Bowel and\u002For bladder incontinence","ALL","18 Years",{"count":74,"type":75},40,"ESTIMATED","INTERVENTIONAL",[78],"NA","The goal of this clinical trial is to see if electrical stimulation applied through the application of a wearable suit improves pain and function among adults with lower-limb amputation who report pain in two or more body regions. The main questions this study seeks to answer are:\n\n* Does the suit provide a viable treatment option for pain management?\n* Does the intensity of electrical stimulation matter? Researchers will compare two different intensities of electrical stimulation applied through application of a wearable suit to see the immediate, sustained and cumulative effects on pain and function among adults with lower-limb amputation.\n\nParticipants will:\n\n* Fill out questionnaires online.\n* Undergo two onsite clinical examinations.\n* Complete 10 treatment sessions over 2-3 weeks.",[81],"Amputation Pain",[83,84,85],"pain","amputation","electrical stimulation","NOT_YET_RECRUITING","2026-08-06",{"date":89,"type":90},"2026-08-12","ACTUAL",{"date":92,"type":75},"2026-09-01",{"date":94,"type":75},"2028-08",{"name":5,"class":6},1]