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NCT07725744Not yet recruiting

Interface Pressures, Safety, Adherence, and Tactile Outcomes of Different Pressure Garments After Stroke

Interface Pressures, Safety, Adherence, and Tactile Outcomes of Different Pressure Garments After Stroke: A Prospective, Participant-Blinded, Three-Arm, Parallel-Group Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 24 Jul 2026

Brief summary (registry, in English)

This study aims to investigate the interface pressure changes of single-layer with 10% circumferential reduction (S-10), single-layer with 15% circumferential reduction (S-15), and dorsal double-layered with 10% circumferential reduction (DD-10)pressure garments over time, their relationships with adherence and adverse events, and their effects on tactile gnosis. Participants will: 1. Wear S-10, S-15, or DD-10 for at least 12 hours daily for four weeks 2. Measure interface pressure at baseline and weekly 3. Assess tactile gnosis at baseline, Week 2, and Week 4 4. Record adherence and adverse events using a self-report logbook

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
33 (estimated)
First submitted
21 Jul 2026
Start date
20 Jul 2026
Primary completion date
31 Jan 2027
Lead sponsor
National University of Malaysia
Diseases
Stroke
NCT number
NCT07725744

What you commit to

  • Study type: Interventional
  • Planned participants: 33
  • From 20 Jul 2026 to the primary completion date, 31 Jan 2027
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • skin lesions, infections or other skin problems
  • serious circulatory problems such as deep vein thrombosis
  • behavioural disturbances or motor impairments caused by other orthopaedic or neurological conditions other than stroke

Other

  • hypersensitive to Lycra materials

Who the study is looking for

  • adults aged between 21 years to 60 years old
  • a history of stroke (no restrictions on the stroke type)
  • Modified Ashworth Scale of 1, 1+ or 2 when hand performing flexion and extension
  • no cognitive impairment (Montreal Cognitive Assessment (MoCA ⩾ 21)

Age in the registry: 21 years to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.