A Reliability And Validity Study Of The Urdu Version Of Spine Functional Index.

Sponsor
Riphah International University (Other)
Overall Status
Completed
CT.gov ID
NCT05239962
Collaborator
(none)
220
1
9.2
24

Study Details

Study Description

Brief Summary

The Aim of the study is to translate Spine Functional Index scale into Urdu Language and to investigate the validity and reliability in Pakistan with the populace of Spinal disorders. Also checks its co-relation with Neck disability Index and Roland-Morris Disability Questionnaire.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    As per the previous recommendations, the Spine Functional Index will be interpreted in urdu language and adapted culturally. Participants will be selected by the convenience sampling technique based on pre-defined inclusion and exclusion criteria from a total of 220 participants with spinal Disorders. To test the reliability of Urdu Version Of Spine Functional Index, Neck Disability Index and Roland-Morris Disability Questionnaire in the inter and intra-observer environment, two observers and an interim interval of 45 minutes between the first and second application fill out a questionnaire on the same day for the inter-observer assessment. Observer-1 for the intra-observer evaluation will conduct a third evaluation after 7 days. Using Statistical Package of Social Sciences version 24, data is entered and analyzed. Cronbach Alpha Value is used to analyze center consistency. The intraclass correlation coefficient is used to assess the reliability of the test-retest. For content validity, criteria validity and responsiveness, the Urdu Version Of Spine Functional Index was assessed.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    220 participants
    Observational Model:
    Ecologic or Community
    Time Perspective:
    Cross-Sectional
    Official Title:
    Evaluation of Reliability and Validity of Urdu Version of Spine Functional Index
    Actual Study Start Date :
    May 30, 2021
    Actual Primary Completion Date :
    Mar 1, 2022
    Actual Study Completion Date :
    Mar 5, 2022

    Outcome Measures

    Primary Outcome Measures

    1. Spine Functional Index [1st day]

      Spine Functional Index is a single page of 25 items with a three-point respond option. The score of 25 items is summed and this score is then multiplied by four and deducted from 100 (0 % score = max disability or functional loss and 100 % score = no impairments or normal).

    2. Roland-Morris Questionnaire [1st day]

      Roland-Morris Questionnaire is a self-administered disability measure in which greater levels of disability are reflected by higher numbers on a 24-point scale.

    3. Neck Disability Index [1st day]

      Neck Disability Index contains total 50 scores. 5 marks for each statement. If the response is missing then the score will not be conducted or included in total marks.

    4. Oswestry Low Back Pain Index [1st day]

      Oswestry Low Back Pain Index is an extremely important tool that researchers and disability evaluators use to measure a patient's permanent functional disability. The test is considered the 'gold standard' of low back functional outcome tools. A score of 0-20 reflects minimal disability, 21-40 moderate disability, 41-60 severe disability, 61-80 crippled, and 81-100 bed-bound.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • The criteria for participation in this study were at least 18 years of age.

    • The patient must be diagnosed with musculoskeletal disorder of the spine.

    • The patient can be chronic and sub-acute and acute.

    • The patient can be referred by a physician or physical therapist.

    Exclusion Criteria:
    • Lack of reading Urdu or reply to the survey questions were the criteria for exclusion.

    • Infectious diseases and patient without spinal disorders were excluded.

    • The patients with late surgery or systemic sickness which effects spine was excluded

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Ripah International University Faisalabad Punjab Pakistan 38000

    Sponsors and Collaborators

    • Riphah International University

    Investigators

    • Study Chair: Muhammad Kashif, Riphah International University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Riphah International University
    ClinicalTrials.gov Identifier:
    NCT05239962
    Other Study ID Numbers:
    • REC/FSD/0289
    First Posted:
    Feb 15, 2022
    Last Update Posted:
    Apr 5, 2022
    Last Verified:
    Apr 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Riphah International University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 5, 2022