Kinesio Taping for Upper Extremity Motor Function in Acute Stroke Patients
KT-AcuteStroke
The Effects of Kinesio Taping on the Upper Extremity Motor Function, Pain, General Health and Depression in Acute Stroke Patients: A Randomized Controlled Trial
1 other identifier
interventional
26
1 country
1
Brief Summary
This randomized, controlled clinical trial was conducted to evaluate the effects of kinesio taping on upper extremity motor recovery in patients with acute ischemic stroke who presented with flaccid muscle tone. Twenty-six adults were randomly assigned to either a kinesio taping group or a sham taping group, in addition to receiving standard rehabilitation. Participants were evaluated at baseline, at the end of the 3-week taping period, and at 6 weeks using validated measures of motor function, pain, general health, and depression. The study aimed to determine whether kinesio taping provides additional benefits beyond conventional rehabilitation in improving motor performance of the wrist and hand, reducing pain, and supporting overall functional and emotional well-being in the early phase of stroke recovery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jun 2018
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
November 10, 2018
CompletedFirst Submitted
Initial submission to the registry
November 30, 2025
CompletedFirst Posted
Study publicly available on registry
December 24, 2025
CompletedDecember 24, 2025
November 1, 2025
3 months
November 30, 2025
December 17, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Fugl-Meyer Wrist, Sitting Position Upper Extremity and Hand Scores
Fugl Meyer Rating Scale (FMRS) was used to evaluate motor function. This scale was developed to evaluate the patient's sensorimotor recovery after stroke by the Brunnstrom motor healing stages. The scale covers the upper extremity in 3 parts: the shoulder-elbow-forearm, the sitting position in the wrist, the hand; and allows the evaluation of reflex activity, synergy patterns and voluntary movements. It is a reliable method for assessing the severity of post-stroke sensorimotor impairment. The maximum total score for the upper extremity in FMRS is 66.
Baseline, Week 3, Week 6
Secondary Outcomes (4)
Change in Brunnstrom Staging (Upper Extremity and Hand)
Baseline, Week 3, Week 6
Change in Visual Analog Scale (VAS) for Hand Pain
Baseline, Week 3, Week 6
Change in Health Assessment Questionnaire (HAQ) Disability Index
Baseline, Week 3, Week 6
Change in Beck Depression Inventory (BDI) Score
Baseline, Week 3, Week 6
Study Arms (2)
Kinesio Taping
EXPERIMENTALParticipants received kinesio taping applied to the dorsum of the hand and forearm using standard facilitation techniques with approximately 25% tension, in addition to conventional rehabilitation.
Sham Taping
SHAM COMPARATORParticipants received sham taping without tension and without crossing joints, mimicking the appearance of kinesio taping but without therapeutic effect, in addition to conventional rehabilitation.
Interventions
Kinesio tape was applied to the dorsum of the hand with five 1-cm I-strips and one 5-cm I-strip extending toward the forearm, with \~25% stretch. Three applications over approximately 3 weeks.
Sham taping was performed using Y- and I-strips without stretch and without crossing joints. Three applications over approximately 3 weeks.
Eligibility Criteria
You may qualify if:
- Adults aged 50-80 years
- Diagnosis of acute ischemic stroke confirmed by CT or MRI
- Within first 6 months after stroke onset
- Brunnstrom Stage 1 for upper extremity and hand (flaccid muscle tone)
- Sufficient cognitive ability to follow instructions
- Participation in inpatient or outpatient stroke rehabilitation
- Ability to provide informed consent
You may not qualify if:
- Hemorrhagic stroke etiology
- Prior upper extremity surgery, fracture, contracture, or heterotopic ossification
- Brachial plexus injury or peripheral nerve lesions
- Additional neurological disorders (e.g., Parkinson's disease, spinal cord injury, polyneuropathy)
- Severe shoulder pain (VAS ≥ 5) that could interfere with assessments
- Significant musculoskeletal disorders affecting the hemiplegic upper extremity
- Uncontrolled comorbidities that prevent participation in rehabilitation
- Inability to complete follow-up assessments
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Koç Universitylead
Study Sites (1)
SB Istanbul Education and Research Hospital
Istanbul, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Havvanur Albayrak
Koç University School of Medicine
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Masking Details
- Participants and outcome assessors were blinded to group allocation
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Specialist Physician, Department of Physical Medicine and Rehabilitation
Study Record Dates
First Submitted
November 30, 2025
First Posted
December 24, 2025
Study Start
June 1, 2018
Primary Completion
September 1, 2018
Study Completion
November 10, 2018
Last Updated
December 24, 2025
Record last verified: 2025-11
Data Sharing
- IPD Sharing
- Will not share