- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05207579
Urdu Version of Lower Extremity Functional Scale: Reliability and Validity Study
May 18, 2022 updated by: Riphah International University
Psychometric Analysis of Urdu Version of Shoulder Pain and Disability Index: A Reliability and Validity Study
The objective of the research is to translate and to culturally familiarize the Lower extremity functional scale into the Urdu language along the investigation if the Lower Extremity Functional Scale is reliable and validate in the Pakistani population with Lower extremity musculoskeletal disorders and to check the correlation with Short Form - 36.
Study Overview
Status
Completed
Conditions
Detailed Description
The questionnaire will be translated into Urdu and cross-culturally modified.
Internal consistency, test-retest reliability, conceptual validity, discriminative validity, responsiveness, and concurrent validity will be examined in 150 participants seeking treatment for lower extremity dysfunction using the Urdu version of the Lower Extremity Functional Scale.
Study Type
Observational
Enrollment (Actual)
150
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
-
-
Punjab
-
Faisalabad, Punjab, Pakistan, 38000
- Ripah International university
-
-
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
16 years to 60 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Pakistani population with Lower extremity musculoskeletal disorders was included in the study.
Description
Inclusion Criteria:
- From16 years Old to 60 Years Old
- Presence of an Lower extremity musculoskeletal disorders like soft tissue injuries, joints and muscles injuries
- No intervention between the test-retest assessments
Exclusion Criteria:
- To complete the forms because of a psychological Impairment.
- Illiteracy or lack of understanding of Urdu Language
- The presence of any kind of bone fracture
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
- Observational Models: Ecologic or Community
- Time Perspectives: Cross-Sectional
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lower Extremity Functional Scale
Time Frame: 1st day
|
Lower Extremity Functional Scale is a valid and reliable instrument to determine the functional status for acute and chronic lower extremity musculoskeletal dysfunction due to the importance of evidence-based health care
|
1st day
|
|
Short Form-36
Time Frame: 1st day
|
Short Form-36 is one of the most widely used and evaluated generic health-related quality of life questionnaires.
|
1st day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
May 30, 2021
Primary Completion (Actual)
April 25, 2022
Study Completion (Actual)
April 28, 2022
Study Registration Dates
First Submitted
January 24, 2022
First Submitted That Met QC Criteria
January 24, 2022
First Posted (Actual)
January 26, 2022
Study Record Updates
Last Update Posted (Actual)
May 19, 2022
Last Update Submitted That Met QC Criteria
May 18, 2022
Last Verified
May 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/FSD/0294
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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