Skip to main content
OpenTrials
Completed

NCT Number: NCT07555847

Effect of Kinesiotaping on Tremor in People With Parkinson's Disease

The goal of this clinical trial is to learn whether adding kinesiotaping to a strengthening and stretching home-exercise program can reduce hand tremor and improve hand function in people with Parkinson's disease. The study will also examine how true kinesiotaping compares with sham (placebo) taping and with exercise alone in improving tremor frequency, grip strength, fine motor skills, motor symptoms, daily living activities, and quality of life.

Adults aged 18-80 with Parkinson's disease and hand tremor will be randomly assigned to one of three groups:

Kinesiotaping + Exercise Group: Participants will receive therapeutic kinesiotaping applied to the forearm extensor muscles and wrist for 4 weeks (twice weekly), in addition to a home program of strengthening and stretching exercises.

Sham Taping + Exercise Group: Participants will receive a placebo taping without tension that does not target specific muscles, along with the same exercise program.

Exercise-Only Group: Participants will complete the same home-exercise program without any taping.

Researchers will compare the three groups to see whether kinesiotaping provides additional benefits beyond exercise and whether it performs better than sham taping. Tremor frequency will be measured using an Apple Watch device, and hand strength, dexterity, motor symptoms, and quality of life will be assessed using validated clinical scales.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Health Sciences, Sultan 2. Abdulhamid Han Training and Research Hospital

Istanbul, Uskudar, 34668, Turkey (Türkiye)

About this study

Resting tremor is one of the main motor symptoms in Parkinson's disease and can significantly limit daily activities, fine motor skills, and upper-extremity function. This clinical trial is designed to evaluate whether adding therapeutic kinesiotaping to a home-based exercise program can reduce hand tremor and improve hand function. The study also aims to compare the effectiveness of true kinesiotaping with sham (placebo) taping and to determine whether either method provides additional benefit beyond exercise alone.

This randomized, controlled, three-arm clinical trial will include participants aged 18 to 80 years who have been diagnosed with Parkinson's disease and experience hand tremor. Participants will be randomly assigned to one of three groups: (1) Kinesiotaping + Exercise, (2) Sham Taping + Exercise, or (3) Exercise Only. All participants will receive a standardized home-exercise program that includes strengthening and stretching exercises targeting forearm muscles. The exercise program will be performed once daily for four weeks.

In the kinesiotaping group, therapeutic taping will be applied to the forearm extensor muscles and wrist using functional taping techniques with appropriate tension and directional application. This approach aims to enhance proprioceptive input, improve muscle activation, and reduce tremor amplitude. In the sham taping group, tape will be applied without therapeutic tension and without following muscle-fiber orientation, providing a placebo intervention. The control group will receive the exercise program only, without any taping.

Tremor severity and frequency will be assessed using accelerometer data from an Apple Watch worn on the affected wrist. Grip strength will be measured with a Jamar dynamometer, and hand dexterity will be evaluated using the Nine Hole Peg Test. Motor symptoms will be assessed with the MDS-UPDRS Part 3, and quality of life will be evaluated using the Parkinson's Disease Questionnaire (PDQ-39). Outcomes will be measured at baseline (T0), at the end of the 4-week intervention (T1), and two weeks after the end of treatment (T2).

The primary objective of this study is to determine whether kinesiotaping provides additional benefit in reducing hand tremor compared with exercise alone. Secondary objectives include evaluating improvements in hand function, changes in grip strength, changes in motor symptoms, and improvements in quality-of-life measures. Kinesiotaping is expected to support tremor control by enhancing proprioceptive feedback. The sham taping group is included to control for placebo effects and to distinguish the specific therapeutic contribution of true kinesiotaping.

This study aims to provide clinical evidence on the usefulness of kinesiotaping as an adjunct to exercise for managing tremor in individuals with Parkinson's disease. The three-arm design will allow clear comparison between true taping, sham taping, and exercise alone, helping to identify the unique effects of kinesiotaping.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of idiopathic Parkinson's disease
  • Hoehn and Yahr stage 1-4
  • Presence of hand tremor
  • Mini-Mental State Examination (MMSE) score ≥ 23
  • Stable medical treatment for at least 3 months prior to enrollment and no planned changes during the study period
  • Age between 18 and 80 years
  • Ability to understand and provide written informed consent

Exclusion criteria

  • Diagnosis of essential tremor or tremor due to causes other than Parkinson's disease
  • Advanced motor impairment (severe bradykinesia or dyskinesia)
  • History of allergic reaction to kinesiotaping materials
  • Presence of other neurological disorders causing tremor (e.g., ALS, multiple sclerosis, cerebellar disorders)
  • Severe psychiatric disorders (e.g., major depression, psychosis, severe anxiety)

Treatment and study plan

Therapeutic Kinesiotaping

Other

Kinesiotaping applied to forearm extensor muscles with therapeutic tension and direction, twice weekly for 4 weeks

Sham Taping

Other

Placebo taping applied without therapeutic tension and without muscle alignment, twice weekly for 4 weeks

Home Exercise Program

Behavioral

Daily strengthening and stretching exercises targeting forearm muscles, performed for 4 weeks.

Primary outcomes

  1. Tremor Frequency (Hz)

    Time frame: Baseline (Day 0), End of treatment (Week 4), and Follow-up (Week 8; 4 weeks after treatment completion)

    Change in dominant tremor frequency measured using Apple Watch sensors (accelerometer and gyroscope) during a standardized 60-second recording period. Lower frequency values indicate improvement in tremor severity.

Secondary outcomes

  1. Hand Grip Strength (kg)

    Time frame: Time Frame: Baseline (Day 0), End of treatment (Week 4), and Follow-up (Week 8; 4 weeks after treatment completion)

    Measured using a Jamar hand dynamometer. Higher values indicate better muscle strength.

  2. Pinch Strength (kg)

    Time frame: Time Frame: Baseline (Day 0), End of treatment (Week 4), and Follow-up (Week 8; 4 weeks after treatment completion)

    Measured using a Jamar pinch meter. Higher values indicate better finger strength.

  3. Fahn-Tolosa-Marin Tremor Rating Scale Score

    Time frame: Time Frame: Baseline (Day 0), End of treatment (Week 4), and Follow-up (Week 8; 4 weeks after treatment completion)

    Clinician-rated scale assessing tremor severity. Scores range from 0 to 144, with higher scores indicating more severe tremor.

  4. Nine-Hole Peg Test

    Time frame: Time Frame: Baseline (Day 0), End of treatment (Week 4), and Follow-up (Week 8; 4 weeks after treatment completion)

    Measures fine motor dexterity and hand coordination. Shorter completion time indicates better performance.

  5. MDS-UPDRS Part III Score

    Time frame: Time Frame: Baseline (Day 0), End of treatment (Week 4), and Follow-up (Week 8; 4 weeks after treatment completion)

    Clinician-rated motor examination assessing severity of Parkinsonian motor symptoms. Scores range from 0 to 132, with higher scores indicating worse motor impairment.

  6. Parkinson's Disease Questionnaire-39 (PDQ-39) Score

    Time frame: Time Frame: Baseline (Day 0), End of treatment (Week 4), and Follow-up (Week 8; 4 weeks after treatment completion)

    Patient-reported quality of life measure. Scores range from 0 to 100, with higher scores indicating worse quality of life.

  7. Barthel Index Score

    Time frame: Time Frame: Baseline (Day 0), End of treatment (Week 4), and Follow-up (Week 8; 4 weeks after treatment completion)

    Measures independence in activities of daily living. Scores range from 0 to 100, with higher scores indicating greater independence.

Sponsors and collaborators

Lead sponsor

Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey

Other

Registry information

Official study title

Effect of Kinesiotaping on Hand Tremor in Patients With Parkinson's Disease: A Randomized Controlled Trial

Important dates

Study start
2025
Primary completion
2025
Study completion
2026
First posted
Apr 29, 2026
Registry last updated
Apr 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.