Effects of Kinesio Taping in Subacute Stroke Patients

NCT ID: NCT07192484

Last Updated: 2025-09-25

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-09-15
• Study Completion Date: 2026-12-31

Brief Summary

A study was designed to investigate the effects of KT on gait ability, balance, and neuromuscular functions in subacute stroke patients with foot drop. The study aims to evaluate the immediate and short-term effects of KT on gait ability, balance, and neuromuscular function in subacute stroke patients with foot drop. A total of 60 participants will be recruited and randomly assigned to either a control group (conventional physical therapy) or an experimental group (receiving additional KT). Both groups will receive 30 minutes of daily physical therapy. The experimental group will undergo an initial assessment before KT application, which includes (1) activation of the dorsiflexor muscles, (2) reduction of plantar flexor spasticity, and (3) stabilization of the ankle in an everted position. After taping, a second assessment will be conducted immediately, and the tape will stay applied to patient's limb for two days, followed by a third assessment. The control group will be assessed only before the intervention and after two days. Primary outcome measures include gait ability (10-meter walk test, laboratory gait parameters, and joint angles and electromyographic activity during walking). Secondary outcomes include balance (Functional reach test, Timed Up and Go test, and Activities-specific Balance Confidence Scale) and neuromuscular function assessments (muscle strength, joint range of motion, spasticity, and proprioception). This project aims to establish and validate a clinically applicable and effective KT protocol as an adjunctive gait training method for subacute stroke patients with foot drop. By enhancing independent and safe walking, this intervention may facilitate the early return to normal daily activities for stroke survivors.

Conditions

Stroke Gait Rehabilitation

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

KT group

Receiving additional Kinesio taping

Group Type: EXPERIMENTAL

KT group

Intervention Type: BEHAVIORAL

Receiving additional KT

Control group

Conventional physical therapy

Group Type: OTHER

Conventional group

Intervention Type: BEHAVIORAL

Conventional physical therapy

Interventions

KT group

Receiving additional KT

Intervention Type: BEHAVIORAL

Conventional group

Conventional physical therapy

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• Age between 20 and 80 years;
• First unilateral stroke;
• Stroke onset between at least 1 week and 1 year;
• Ability to continuously walk 10 meters with or without assistive devices;
• Presence of foot drop on the affected side during the swing phase due to insufficient ankle dorsiflexion;
• Brunnstrom stage of the affected lower limb ≥ 3;
• Presence of mild spasticity in the affected ankle plantar flexors, with a Modified Ashworth Scale score ≤ 2;
• Ability to follow simple commands

Exclusion Criteria

• Other neurological disorders or unstable medical conditions;
• Skin allergies that interfere with the use of tape;
• Visual field defects;
• Cognitive impairment, defined as a Mini-Mental State Examination (MMSE) score < 24;
• Pusher syndrome;
• Ankle contracture;
• Hemispatial neglect;
• Poorly controlled hypertension or cardiovascular disease;
• Any other disease, apart from stroke, that may affect balance or gait.

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Fooyin University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Central Contacts

I-Hsuan Chen

Role: CONTACT

Y0894@fy.edu.tw

886-7-7811151 #7043

Other Identifiers

KSVGH25-CT6-22

Identifier Type: -

Identifier Source: org_study_id