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NCT05263128 Clinical Trial

Turkish Version of the Hand20 Questionnaire With Carpal Tunnel Syndrome

Carpal Tunnel Syndrome Clinical Trial

Official title:
Validity Study of the Turkish Version of the Hand20 Questionnaire With Carpal Tunnel Syndrome

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT05263128
Other study ID # Hasan Kalyoncu Universty
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date August 1, 2022
Est. completion date December 1, 2024

Study information
Verified date September 2023
Source Hasan Kalyoncu University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The questionnaire will be investigated by administering the Hand-20 questionnaire and the Boston Carpal Tunnel Syndrome Questionnaire to patients with carpal tunnel syndrome, one week apart.

Description:

Questionnaires, which are used to express the perception of difficulty and hand functionality during daily living activities of individuals with carpal tunnel syndrome, and most importantly, which are easy to administer, should be preferred in order to plan a patient-specific treatment program with these results. Self-administered questionnaires showing the physical dimension of recovery are effective and sensitive to change. Hand20 is a short, easy-to-understand and visual questionnaire used to evaluate disorders caused by upper extremity pathologies, developed by Suzuki et al. in 2010 and proven to be valid in upper extremity diseases by Töre et al. In this questionnaire consisting of 20 questions, the answer to each question is graded between 0 and 10 (0: No restrictions, 10: Impossible). The best score is 0, the worst score is 100. Boston carpal tunnel syndrome questionnaire (BKTSA) will be used to evaluate the functionality level and symptom severity of the patients. In this questionnaire, which consists of 2 parts: symptom severity and functional capacity, a separate average score will be calculated for each part by dividing the total score obtained by the number of questions. An increased score indicates decreased functional capacity and increased symptom severity.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date December 1, 2024
Est. primary completion date May 1, 2024
Accepts healthy volunteers
Gender All
Age group 25 Years to 60 Years
Eligibility Inclusion Criteria: - Patients aged 25-60 years - Patients diagnosed with carpal tunnel - Patients who volunteered for treatment Exclusion Criteria: - Patients who do not agree to volunteer - Patients who have undergone surgery from the wrist region

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Investigation of the validity of the Hand-20 Questionnaire in individuals with carpal tunnel syndrome
To investigate the validity and reliability of the Hand-20 questionnaire used in individuals with upper extremity disease by comparing it with the Boston carpal tunnel syndrome questionnaire in individuals with carpal tunnel syndrome in Turkey

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Hasan Kalyoncu University

Outcome
Type Measure Description Time frame Safety issue
Primary Investigation of the Validity of the Hand-20 Questionnaire in Individuals with Carpal Tunnel Syndrome 1 week apart
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