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Carpal Tunnel Syndrome (CTS)NCT06758193

Validity and Reliability of the MAP-Hand Scale in Patients With Carpal Tunnel Syndrome

An observational study of Carpal Tunnel Syndrome (CTS), run by Kirsehir Ahi Evran Universitesi at 1 site in Turkey (Türkiye).

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Carpal Tunnel Syndrome (CTS)
How many people
180 participants
Where
1 siteTurkey (Türkiye)
Study dates
10 Dec 2024to 1 Aug 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

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.

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Turkey (Türkiye)1 site
  • Kirsehir Ahi Evran University

    Kırşehir, Merkez, 40100

Other trials in Turkey (Türkiye)

About this study

Official title: 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.

Being tested
No intervention was applied in this study.
Keywords
Carpal Tunnel Syndrome, Reliability, Validity
Medical subject headings
Carpal Tunnel Syndrome

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • No intervention was applied in this study.Other

    No intervention was applied in this study.

Study groups in NCT06758193
Study groupRoleWhat they receive
Study GroupNot described
Receives: Other: No intervention was applied in this study.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Hand Activity Performance

    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.

    Measured: 24 weeks

Secondary outcomes (5)
  1. Grip Strength

    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.

    Measured: 24 weeks

  2. Pain measurement

    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.

    Measured: 24 weeks

  3. Hand and Finger Skills

    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.

    Measured: 24 weeks

  4. Hand Health Status

    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.

    Measured: 24 weeks

  5. Carpal Tunnel Symptom Severity

    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.

    Measured: 24 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Jan 2025
  2. Study start10 Dec 2024
  3. Primary completion1 May 2026 (estimated)
  4. Study completion1 Aug 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
180 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06758193
Sponsor's protocol ID
KAEU-T.ATAHAN-006
Status last verified
Jun 2025
First submitted
26 Dec 2024
Last updated
22 Apr 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Carpal Tunnel Syndrome (CTS), run by Kirsehir Ahi Evran Universitesi at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 22 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Hand Activity Performance (time frame: 24 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Apr 2026.

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