[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100644505":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":26,"locations":26,"responsibleParty":31,"collaborators":26,"id":35,"slug":36,"hasResults":37,"nctId":38,"briefTitle":39,"officialTitle":40,"acronym":41,"eligibilityCriteria":42,"healthyVolunteers":37,"sex":43,"minAge":44,"maxAge":45,"enrollmentInfo":46,"targetDuration":26,"studyType":49,"phases":50,"briefSummary":52,"conditions":53,"keywords":55,"overallStatus":60,"whyStopped":26,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":26},{"fullName":5,"class":6},"Imam Abdulrahman Al Faisal Hospital","OTHER_GOV",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Multisensory Re-education Group","EXPERIMENTAL","Participants will receive a structured multisensory re-education program targeting sensory deficits associated with diabetic peripheral neuropathy. The intervention will be delivered twice weekly for five weeks and will include tactile, thermal, vibration, proprioceptive, and sensory discrimination training.",[13],"Behavioral: Structured Multisensory Re-education Program",{"label":15,"type":16,"description":17,"interventionNames":18},"Sham Control Group","SHAM_COMPARATOR","Participants will receive sham sensory exposure sessions without active sensory retraining. The frequency and duration of sessions will match the experimental group.",[19],"Behavioral: Behavioral: Sham Sensory Exposure",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"BEHAVIORAL","Structured Multisensory Re-education Program","A structured multisensory re-education program targeting sensory deficits in individuals with diabetic peripheral neuropathy. The program includes tactile, thermal, vibration, proprioceptive, and sensory discrimination training delivered twice weekly for five weeks.",[9],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Behavioral: Sham Sensory Exposure","Participants in the sham control group will receive passive sensory exposure sessions without structured sensory re-education, active sensory discrimination training, feedback, or progression of sensory tasks. The duration and frequency of sessions will be matched to the experimental group.",[15],{"type":32,"investigatorFullName":33,"investigatorTitle":34,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"PRINCIPAL_INVESTIGATOR","Turki Abualait","Associate Professor, Department of Physical Therapy, Imam Abdulrahman Bin Faisal University","100644505","efficacy-of-a-structured-multisensory-re-education-program-on-sensory-function-and-upper-limb-sensorimotor-performance-in-individuals-with-diabetic-peripheral-neuropathy-100644505",false,"NCT07670598","Efficacy of a Structured Multisensory Re-education Program on Sensory Function and Upper Limb Sensorimotor Performance in Individuals With Diabetic Peripheral Neuropathy.","Efficacy of a Structured Multisensory Re-education Program on Sensory Function and Upper Limb Sensorimotor Performance in Individuals With Diabetic Peripheral Neuropathy: A Randomized Sham-Controlled Trial.","SENS-UL","InclusioInclusion Criteria:\n\nAdults aged 18 to 75 years. Clinically confirmed diabetic peripheral neuropathy (DPN). Stable medical condition and medication regimen for at least 3 months. Ability to understand study procedures and provide informed consent. Ability to participate in upper-limb sensory and sensorimotor assessments. Willingness to attend all intervention sessions and follow study instructions.\n\nExclusion Criteria:\n\nOther neurological disorders affecting sensory or motor function (e.g., stroke, multiple sclerosis, Parkinson's disease).\n\nSevere visual, auditory, or cognitive impairment interfering with participation.\n\nUpper-limb musculoskeletal conditions limiting hand function or assessment performance.\n\nActive foot ulcer, severe diabetic complications, or unstable medical condition.\n\nParticipation in another rehabilitation or clinical trial during the study period.\n\nPregnancy.\n\nInability to comply with study procedures or follow-up assessments.n Criteria:\n\nExclusion Criteria:\n\n\\-","ALL","18 Years","75 Years",{"count":47,"type":48},59,"ESTIMATED","INTERVENTIONAL",[51],"NA","Diabetic Peripheral Neuropathy (DPN) is a common complication of diabetes that can cause impairments in sensation, dexterity, and upper-limb function. Current treatment approaches mainly focus on symptom management and glycemic control, while interventions specifically targeting sensory recovery remain limited.\n\nThis randomized sham-controlled trial aims to evaluate the effectiveness of a Structured Multisensory Re-education Program (SENS-UL) in improving sensory function and upper-limb sensorimotor performance in adults with DPN. Participants will be randomly assigned to either an intervention group receiving structured multisensory sensory re-education or a sham-control group receiving passive sensory exposure without active sensory retraining.\n\nThe intervention will be delivered twice weekly for five weeks. Outcome measures will include sensory function, neuropathy severity, thermal and tactile sensation, vibration perception, proprioception, dexterity, and neuropathy-related quality of life. Assessments will be conducted before and after the intervention period.\n\nThe study is expected to provide evidence regarding the effectiveness of multisensory sensory rehabilitation for individuals with DPN and may contribute to the development of targeted rehabilitation strategies aimed at improving sensory recovery, hand function, and quality of life.",[54],"Diabetic Peripheral Neuropathy",[56,57,58,59],"Multisensory Rehabilitation","Sensorimotor Function","Upper Limb Function","Quality of Life","NOT_YET_RECRUITING","2026-06-25",{"date":63,"type":64},"2026-06-26","ACTUAL",{"date":66,"type":48},"2026-09-01",{"date":68,"type":48},"2028-09-30",{"name":5,"class":6}]