- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06191705
Urdu Translation, Validity and Reliability of Quick Disabilities of Arm, Shoulder & Hand (QuickDASH)
December 20, 2023 updated by: Foundation University Islamabad
The purpose of this study is to translate Quick Disabilities of Arm, Shoulder & Hand (QuickDASH) into Urdu and determine the validity and reliability of the Urdu version of QuickDASH.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
50
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Muhammad Osama
- Phone Number: +923325540436
- Email: osamadpt@gmail.com
Study Locations
-
-
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Islamabad, Pakistan, 66000
- Foundation University Islamabad
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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
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
Individuals with for shoulder, arm/wrist, or hand musculoskeletal injury/pain/symptoms.
Description
Inclusion Criteria:
Individuals with for shoulder, arm/wrist, or hand musculoskeletal injury/pain/symptoms. Capable of understanding and completing the self-reported questionnaires. The exclusion criteria were the -
Exclusion Criteria:
Presence of any systemic disease or any neurological disorder. The upper limb involvement is due to any recent surgery in less than 6 weeks.
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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 |
|---|---|
|
Individuals with Arm, Shoulder or Hand pain /symptoms.
|
Participants will be administered Urdu version of QuickDASH to collect data regarding Disabilities of Arm, Shoulder & Hand twice with a time interval of 72 hours to determine validity and reliability.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
QuickDASH
Time Frame: 72 hours
|
Quick Disabilities of Arm, Shoulder & Hand (QuickDASH) is used to determine the Disabilities of Arm, Shoulder and Hand.
A higher score signifies poor outcome.
|
72 hours
|
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 (Estimated)
April 1, 2024
Primary Completion (Estimated)
December 1, 2024
Study Completion (Estimated)
December 1, 2024
Study Registration Dates
First Submitted
December 20, 2023
First Submitted That Met QC Criteria
December 20, 2023
First Posted (Actual)
January 5, 2024
Study Record Updates
Last Update Posted (Actual)
January 5, 2024
Last Update Submitted That Met QC Criteria
December 20, 2023
Last Verified
December 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- FUI/CTR/2023/26
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
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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