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Translation, Cultural Adaptation and Validation of Urdu Version of VISA-A Questionnaire

Sponsor
University of Lahore (Other)
Overall Status
Completed
CT.gov ID
NCT05125198
Collaborator
(none)
80
Enrollment
1
Location
6.4
Actual Duration (Months)
12.4
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This study is designed to translate and validate the VISA-A questionnaire to the Urdu language, to interpret its psychometric properties, and to determine the reliability of scores obtained from the population of Pakistan. The translated version of the gold standard tool will be used by the local population as well as Urdu-speaking immigrants across the globe to better understand and report the severity of their symptoms. Hence, to improve quality of life across cultures, there is a need of standard outcome measures in Urdu language.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    80 participants
    Observational Model:
    Other
    Time Perspective:
    Cross-Sectional
    Official Title:
    Translation, Cultural Adaptation, and Validation of Urdu Version of Victorian Institute of Sports Assessment - Achilles (VISA-A) Questionnaire for Athletes With Achilles Tendinopathy
    Actual Study Start Date :
    Jun 17, 2021
    Actual Primary Completion Date :
    Dec 15, 2021
    Actual Study Completion Date :
    Dec 30, 2021

    Outcome Measures

    Primary Outcome Measures

    1. Change being assessed in interpretation of Severity of Achilles tendinopathy.among participants using translated version of VISA-A questionnaire. [1 week]

      VISA-A is consisted of eight questions that measured the domains of pain, function in daily living, and sporting activity. Results range from 0 to 100, where 100 represents the perfect score

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:

    • Individuals aged over 18 years and both genders.

    • Athletic population with the diagnosis of unilateral mid-portion or insertional Achilles tendinopathy, paratendinosis, partial tendon rupture with or without retrocalcaneal bursitis.

    • With positive Painful arc sign and Royal London Hospital Test.

    • Healthy individuals.

    Exclusion Criteria:

    • Complete rupture of Achilles tendon,

    • Pregnant women and those with any history of radicular pain or lower extremity injury

    • Previous surgery

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The University of Lahore Lahore Punjab Pakistan 54000

    Sponsors and Collaborators

    • University of Lahore

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Sana Akram, Assistant Professor (University Institute of Physical Therapy), University of Lahore
    ClinicalTrials.gov Identifier:
    NCT05125198
    Other Study ID Numbers:
    • ULahore
    First Posted:
    Nov 18, 2021
    Last Update Posted:
    Jan 19, 2022
    Last Verified:
    Jan 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Sana Akram, Assistant Professor (University Institute of Physical Therapy), University of Lahore
    Achilles tendinopathy
    Validity
    Reliability
    Translation
    VISA-A
    Additional relevant MeSH terms:
    Tendinopathy

    Study Results

    No Results Posted as of Jan 19, 2022