MedPath

Effect of Kinesiotaping and Night Splinting in Patients With Carpal Tunnel Syndome

Not Applicable
Completed
Conditions
Carpal Tunnel Syndrome
Interventions
Other: Night Splinting
Other: Kinesiotaping
Other: Control Group
Registration Number
NCT04993703
Lead Sponsor
Hacettepe University
Brief Summary

Carpal tunnel syndrome (CTS) which is defined as a symptomatic compression neuropathy of the median nerve at the level of the wrist.

Different types of splints are used for improving the function and decreasing the pain intensity and symptoms in the rehabilitation of patients with CTS.

However effectiveness of treatment by taping has never been investigated in physiotherapy and rehabilitation.

The aim of this study was to compare the short-term effect of conventional physiotherapy only, and also kinesio taping and night splinting in patients with CTS.

Detailed Description

Carpal tunnel syndrome (CTS) which is defined as a symptomatic compression neuropathy of the median nerve at the level of the wrist.It is considered as the most common disabling neuromuscular condition of the upper extremities.

Night splints are used in conjunction with the conservative intervention to improve the function and decrease the pain intensity and paresthesia in the rehabilitation of patients with carpal tunnel syndrome. However effectiveness of treatment by kinesiotaping has never been investigated.

The aim of this study was to compare the short-term effect of conventional physiotherapy only, and also kinesio taping and night splinting in addition to conventional physiotherapy in the rehabilitation of patients with CTS.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
45
Inclusion Criteria
  • This study included patients with moderate CTS, confirmed by electroneurographic examination.
  • did not recruit any treatment (including physiotherapy or surgical release)
Read More
Exclusion Criteria
  • Patients suffer from the thenar muscle atrophy.
  • Patients with mild CTS.
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Night splintingNight SplintingA total of 20 sessions physiotherapy sessions including hot pack, ultrasound and exercise program (tendon and nerve gliding exercises=2 times per day 3sets of ten repetitions) will be applied. Additionally, night splinting will be advised. Patients will request to keep their splints at nights throughout the study.
KinesiotapingKinesiotapingA total of 20 sessions physiotherapy sessions including hot pack, ultrasound and exercise program (tendon and nerve gliding exercises=2 times per day 3sets of ten repetitions) will be applied. Additionally for this group, kinesiotaping will be applied by using carpal tunnel technique including button hole and I band technique of space correction; and with 25-50% tension in center of tape over dorsal carpal tunnel at the end of the each session. Patients will request to keep kinesiotaping at nights throughout the study.
Control groupControl GroupA total of 20 sessions physiotherapy sessions including hot pack, ultrasound and exercise program (tendon and nerve gliding exercises=2 times per day 3sets of ten repetitions) will be applied.
Primary Outcome Measures
NameTimeMethod
functional impairmentfunctional impairment will be recorded at baseline and 4-week follow-up

functional impairment will be assessed by using Boston Carpal Tunnel Questionnaire. The score consisted of two sub-scales; The Symptom Severity Scale including 11 questions and The Functional Capacity Scale including 8 questions. Each scale score is calculated by the average values of the questions. The scores vary between "1-point" to "5-point". High score indicates severe symptoms and impaired functional capacity.

Secondary Outcome Measures
NameTimeMethod
paresthesiachange from baseline to 4-week follow-up will be recorded

Paresthesia will be assessed by using Visual Analog Scale at rest, activity and at night.

All patients were asked to mark their paresthesia level that corresponds to their paresthesia intensity on the line between "0=no paresthesia" and "100=the worst paresthesia imaginable".

pain intensitychange from baseline to 4-week follow-up will be recorded

pain intensity will be assessed by using Visual Analog Scale at rest, activity and at night.

All patients were asked to mark their pain level that corresponds to their pain intensity on the line between "0=no pain" and "100=the worst pain imaginable".

Trial Locations

Locations (1)

Hacettepe University, Faculty of Physical Therapy and Rehabilitation

🇹🇷

Ankara, Turkey

© Copyright 2025. All Rights Reserved by MedPath