- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04706351
Arabic Version of Identification of Functional Ankle Instability Questionnaire
January 26, 2021 updated by: Aya Abdelhamied Mohamed Khalil, Cairo University
The Arabic Version of Identification of Functional Ankle Instability Questionnaire(IdFAI-Ar)
Testing the validity and reliability of IdFAI
Study Overview
Detailed Description
reliability & validity of Identification Functional Ankle Instability Questionnaire (IdFAI) Arabic version were assessed in reference to Lower Extremity Functional Scale among repeated ankle sprains college students in Cairo.
These college students were randomly selected from different colleges in Cairo University
Study Type
Observational
Enrollment (Actual)
86
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
-
-
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Giza, Egypt, 1216
- Cairo university
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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
18 years to 24 years (Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
male and female college students
Description
Inclusion Criteria:
- eighty six male and female college students will voluntarily participate in the study
Exclusion Criteria:
- Previous ankle surgery.
- History of any ankle surgery.
- History of fracture within the last 6 months.
- Been involved in any previous strengthening or athletic training program.
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: Other
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Validity
Time Frame: 3 months
|
Correlation coefficient
|
3 months
|
|
Reliability
Time Frame: 3 months
|
Cronbach's Alpha
|
3 months
|
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)
March 10, 2018
Primary Completion (Actual)
January 22, 2020
Study Completion (Actual)
January 22, 2020
Study Registration Dates
First Submitted
January 10, 2021
First Submitted That Met QC Criteria
January 10, 2021
First Posted (Actual)
January 12, 2021
Study Record Updates
Last Update Posted (Actual)
January 27, 2021
Last Update Submitted That Met QC Criteria
January 26, 2021
Last Verified
January 1, 2021
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- P.T REC/012/001829
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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