- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06758193
Validity and Reliability of the MAP-Hand Scale in Patients With Carpal Tunnel Syndrome
April 17, 2026 updated by: Atahan TURHAN, Kirsehir Ahi Evran Universitesi
Validity and Reliability of the The Measure of Activity Performance of the Hand Scale in Patients With Carpal Tunnel Syndrome
The primary aim of the study was to determine the validity and reliability of the "MAP-Hand (Measure of Activity Performance of the Hand)" scale in patients with carpal tunnel syndrome.
The secondary aim of the study was to evaluate the hand activity performance in patients with carpal tunnel syndrome.
Study Overview
Status
Enrolling by invitation
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
180
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Merkez
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Kırşehir, Merkez, Turkey (Türkiye), 40100
- Kirsehir Ahi Evran University
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
Patients who apply to the Physical Medicine and Rehabilitation Polyclinic with complaints of hand-wrist pain will be examined by a physical therapist.
Patients who are diagnosed with Carpal Tunnel Syndrome through physical examination, meet the inclusion criteria, and agree to participate in the study will be included in the study.
Description
Inclusion Criteria:
- Age 18 and above and able to read and write
- Diagnosed with mild or moderate unilateral CTS according to electroneuromyography results at least 6 months ago
- Motor-sensory symptoms such as numbness and loss of strength in the hand for at least three months
- Volunteers with no history of diabetes, no medical treatment or injections, no surgery, and no cervical radiculopathy or polyneuropathy
Exclusion Criteria:
- Those with trauma, deformity, fracture, muscle contracture and atrophy in the shoulder, forearm and hand
- Those who have received corticosteroid injections into the carpal tunnel area within the last three months and have been included in a physiotherapy program
- Those who have cognitive problems
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Study Group
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No intervention was applied in this study.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hand Activity Performance
Time Frame: 24 weeks
|
The MAP-Hand (Measure of Activity Performance of the Hand) scale is a scale consisting of 18 items that evaluates the activity performance of the hand.
These items are scored between 1 and 4 and the total score ranges from 18 to 72.
Lower scores indicate better activity performance.
The participants' hand activity performance will be evaluated with the MAP-Hand scale.
The reliability and validity of the Turkish form of the MAP-Hand scale was conducted by Bayraktar and colleagues.
However, their work has not yet been published.
The necessary permissions have been obtained to use the scale.
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24 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Grip Strength
Time Frame: 24 weeks
|
Hand grip strength will be measured with a Camry brand digital dynamometer.
Participants will be assessed in an upright position on a chair with their feet on the floor, with their arm next to their body, elbow in 90-degree flexion, forearm in midrotation and wrist in neutral.
Participants were verbally encouraged during the test.
Measurements were repeated three times and the highest value will be recorded in kilograms.
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24 weeks
|
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Hand and Finger Skills
Time Frame: 24 weeks
|
The participants' hand and finger skills will be tested with the 9-Hole Peg Test (9-DÇT).
The 9-DÇT is a test that measures hand and finger skills in daily life.
A pegboard with 9 holes, 3.2 cm wide, each hole 1.3 cm deep, will be placed in front of the participants in a way that it will be in the midline of the body.
Participants will be asked to randomly place 9 wooden pins on the 9-hole pegboard as quickly as possible and then remove the pins from the pegboard one by one and put them in the box.
At the end of 3 trials, the times will be recorded in seconds with a stopwatch and the shortest time will be recorded.
A longer time to complete the test indicates inadequacy in hand-finger skills.
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24 weeks
|
|
Hand Health Status
Time Frame: 24 weeks
|
Hand health status will be assessed with the "Michigan Hand Outcome Questionnaire (MESA)".
MESA consists of 37 questions and is a questionnaire with 6 parameters that evaluate general hand function, daily living activities, pain, work, aesthetics and satisfaction.
Each question is evaluated with a 5-point Likert scale and a high score indicates a good status.
|
24 weeks
|
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Carpal Tunnel Symptom Severity
Time Frame: 24 weeks
|
The symptom severity and functional status of the participants will be evaluated with the "Boston Carpal Tunnel Syndrome Questionnaire (BCTQ)".
BCTQ consists of the symptom severity scale (SSS) and the functional status scale (FSS) that evaluate the patient in two categories.
While the SSS consists of 11 items, the FSS consists of 8 items.
The average score is calculated by the ratio of the total score obtained to the number of questions.
An increase in the average score indicates that the symptom is severe and functional limitation increases.
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24 weeks
|
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Pain measurement
Time Frame: 24 weeks
|
The participants' pain intensity during rest, activity and night will be measured with VAS.
According to VAS, pain intensity is evaluated on a 10 cm line between 0 (no pain) and 10 (most severe pain).
High scores indicate severe pain.
Participants will be asked to indicate the intensity of pain they feel on a 10 cm scale.
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24 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 10, 2024
Primary Completion (Estimated)
May 1, 2026
Study Completion (Estimated)
August 1, 2026
Study Registration Dates
First Submitted
December 26, 2024
First Submitted That Met QC Criteria
December 26, 2024
First Posted (Actual)
January 3, 2025
Study Record Updates
Last Update Posted (Actual)
April 22, 2026
Last Update Submitted That Met QC Criteria
April 17, 2026
Last Verified
June 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KAEU-T.ATAHAN-006
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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