NCT06587308 Effects of Different Pressure Garments on Upper Extremity Sensorimotor Functions and Quality of Life After Stroke
| NCT ID | NCT06587308 |
| Status | Recruiting |
| Phase | — |
| Sponsor | National University of Malaysia |
| Condition | Cerebral Vascular Accident (CVA)/Stroke |
| Study Type | INTERVENTIONAL |
| Enrollment | 165 participants |
| Start Date | 2024-10-08 |
| Primary Completion | 2026-08 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 165 participants in total. It began in 2024-10-08 with a primary completion date of 2026-08.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The study aims to compare the effects of dorsal-double-layered 10% circumferential reduction (DD-10), single-layered 10% circumferential reduction (S-10), and single-layered no circumferential reduction (S-0) pressure garments on sensorimotor functions, including motor control, dexterity, muscle tone, pain, self-perceived upper extremity function, and quality of life among stroke patients during the 8 weeks of application (Time 1: Baseline, Time 2: Week 4, Time 3: Week 8).
Eligibility Criteria
Inclusion Criteria: * Between 18 and 80 years of age * Within 1-12 months of ischemic or hemorrhagic stroke * First onset resulting in hemiparesis of a limb with Burnnstrom stage of 3, 4 or 5 * Modified Ashworth Scale with scores of less than or equal 2 for elbow, wrist, and hand muscle tone in the affected upper extremity * Able to understand instruction Exclusion Criteria: * Serious cardiovascular or respiratory diseases * Skin lesions, infections or other skin problems * Serious circulatory problems such as deep vein thrombosis * Allergies or significant discomfort to pressure garment materials * Upper extremity fractures or severe joint problems * Severe cognitive impairment with Saint Louis University Mental Status (SLUMs) scores equal to or less than 27 (above high school level of education)/25 (below high school level of education)
Contact & Investigator
SIaw Chui Chai, PhD
PRINCIPAL INVESTIGATOR
Occupational Therapy Programme, Centre for Rehabilitation and Special Needs Studies (iCaRehab)
Frequently Asked Questions
Who can join the NCT06587308 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 80 Years, studying Cerebral Vascular Accident (CVA)/Stroke. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06587308 currently recruiting?
Yes, NCT06587308 is actively recruiting participants. Contact the research team at P126687@siswa.ukm.edu.my for enrollment information.
Where is the NCT06587308 trial being conducted?
This trial is being conducted at Weifang, China, Weifang, China, Weifang, China.
Who is sponsoring the NCT06587308 clinical trial?
NCT06587308 is sponsored by National University of Malaysia. The principal investigator is SIaw Chui Chai, PhD at Occupational Therapy Programme, Centre for Rehabilitation and Special Needs Studies (iCaRehab). The trial plans to enroll 165 participants.
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