- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07249177
Upper Extremity Functional Index in Carpal Tunnel Syndrome
November 24, 2025 updated by: UMUT ERASLAN, Pamukkale University
Validity and Reliability of the Upper Extremity Functional Index in Patients With Carpal Tunnel Syndrome
The aim of this study was to investigate the validity and reliability of the Upper Extremity Functional Index in patients with carpal tunnel syndrome.
This cross-sectional study included 101 patients diagnosed with carpal tunnel syndrome at a university hospital.
Patients were administered the Upper Extremity Functional Index, Michigan Hand Outcomes Questionnaire, and Boston Carpal Tunnel Questionnaire surveys.
Test-retest reliability, internal consistency, and construct validity of the Upper Extremity Fuctional Index were evaluated.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
101
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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Denizli, Turkey (Türkiye), 20170
- Pamukkale 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
Non-Probability Sample
Study Population
This study included patients aged 18-65 years who were diagnosed with carpal tunnel syndrome after visiting the neurology outpatient clinic of a university hospital, who volunteered, who had no history of other trauma, disease, or surgery in the affected limb, and who had no communication difficulties.
The patients were included before starting any conservative or surgical treatment programme.
Description
Inclusion Criteria:
- To be diagnosed with carpal tunnel syndrome, to be a volunteer, and to be between the ages of 18 and 65 years.
Exclusion Criteria:
- no history of other trauma, disease or surgery in the affected limb and difficulty communicating
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 |
|---|---|
|
Patients aged 18-65 years diagnosed with carpal tunnel syndrome.
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The Upper Extremity Functional Index (at the first session and after 2 weeks), the Michigan Hand Outcomes Questionnaire and the Boston Carpal Tunnel Questionnaire were administered to patients using a face-to-face assessment method.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Upper Extremity Functional Index
Time Frame: The questionnaire was administered at baseline (after diagnosis of carpal tunnel syndrome) and 15 days after the baseline assessment.
|
It is a 20-item scale scored using a 4-point Likert scale (0 = Extremely difficult/I cannot do it, 4 = I do not experience any difficulty).
The patient scores between 0 and 80, and it is recommended that the total score be used in studies.
A high score indicates that the patient has good upper extremity function.
|
The questionnaire was administered at baseline (after diagnosis of carpal tunnel syndrome) and 15 days after the baseline assessment.
|
|
Michigan Hand Outcomes Questionnaire
Time Frame: The questionnaire was administered at baseline (after diagnosis of carpal tunnel syndrome)
|
This questionnaire evaluates the functionality of the hand and consists of 63 questions in total.
Each question is scored between 1-5 and the score of each section varies between 0-100.
High total score indicates high satisfaction.
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The questionnaire was administered at baseline (after diagnosis of carpal tunnel syndrome)
|
|
Boston Carpal Tunnel Questionnaire
Time Frame: The questionnaire was administered at baseline (after diagnosis of carpal tunnel syndrome)
|
It has been developed to assess the severity of symptoms and functional status in patients with carpal tunnel syndrome.
The symptom severity scale consists of 11 questions, while the functional status scale consists of 8 questions.
Each question is scored between 1 and 5.
A higher symptom severity or functional status score indicates worse symptoms or functional impairment.
|
The questionnaire was administered at baseline (after diagnosis of carpal tunnel syndrome)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Aytar A, Yuruk ZO, Tuzun EH, Baltaci G, Karatas M, Eker L. The Upper Extremity Functional Index (UEFI): cross-cultural adaptation, reliability, and validity of the Turkish version. J Back Musculoskelet Rehabil. 2015;28(3):489-95. doi: 10.3233/BMR-140545.
- Sousa RL, Moraes VY, Zobiole AF, Nakachima LR, Belloti JC. Diagnostic criteria and outcome measures in randomized clinical trials on carpal tunnel syndrome: a systematic review. Sao Paulo Med J. 2023 Apr 17;141(6):e2022086. doi: 10.1590/1516-3180.2022.0086.07022023. eCollection 2023.
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)
June 28, 2021
Primary Completion (Actual)
November 18, 2022
Study Completion (Actual)
November 18, 2022
Study Registration Dates
First Submitted
November 17, 2025
First Submitted That Met QC Criteria
November 24, 2025
First Posted (Actual)
November 25, 2025
Study Record Updates
Last Update Posted (Actual)
November 25, 2025
Last Update Submitted That Met QC Criteria
November 24, 2025
Last Verified
November 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Nervous System Diseases
- Wounds and Injuries
- Neuromuscular Diseases
- Peripheral Nervous System Diseases
- Median Neuropathy
- Mononeuropathies
- Nerve Compression Syndromes
- Cumulative Trauma Disorders
- Sprains and Strains
- Carpal Tunnel Syndrome
- Health Care Quality, Access, and Evaluation
- Investigative Techniques
- Epidemiologic Methods
- Data Collection
- Health Care Evaluation Mechanisms
- Quality of Health Care
- Public Health
- Environment and Public Health
- Surveys and Questionnaires
Other Study ID Numbers
- E-60116787-020-28687
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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