A Reliability and Validity Study of Urdu Version of Knee Outcome Survey-Activities of Daily Living Scale

NCT ID: NCT05221047

Last Updated: 2022-07-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

150 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-05-30

Study Completion Date

2022-02-28

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this study is to translate Knee Outcome Survey-Activities of Daily Living Scale into Urdu language and to check the reliability and validity of the Knee Outcome Survey-Activities of Daily Living Scale in Urdu language for the general population of Pakistan

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Approximately 150 participants will be included in the study on the basis of inclusion and exclusion criteria. The English version of the Knee Outcome Survey-Activities of Daily Living Scale will be translated and culturally adapted as per as previous recommendations. In the general population with knee pain,Urdu version of the Knee Outcome Survey-Activities of Daily Living Scale will be distributed among general participants by choosing convenience sampling technique based on predefined inclusion and exclusion criteria. To test inter and intra-observer reliability of the final Urdu version of Knee Outcome Survey-Activities of Daily Living Scale with Knee osteoarthritis outcome survey and Lysholm knee score will be filled within same day, by two observers and for the inter-observers assessment, with an interval of 30 minutes between the first and second application. Third assessment will carry out after 7 days by Observer-1(re-intra-observers assessment. Data will be entered and analyzed by Cronbach alpha value.Test-retest reliability will be assessed using interclass correlation coefficient.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Knee Pain

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

ECOLOGIC_OR_COMMUNITY

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Ability to walk without assistive device
* proficiency in the Urdu language
* pain level of at least 30% on the visual analog scale

Exclusion Criteria

* Other osteoarthropathies with a good history
* If you have a heart condition or are having trouble with your nerves
* A debilitating factor that lowers functional independence and activity levels
* A lower-extremity fracture within the previous six months of the research
* Other joint diseases include ligament, menisci, or patellofemoral issues, as well as severe non-osteoarthritic knee effusion or arthroplasty
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Riphah International University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Muhammad Kashif

Role: STUDY_CHAIR

Riphah International University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Ripah International University

Faisalabad, Punjab Province, Pakistan

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Pakistan

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

REC-FSD-00298

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.