- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04368754
Validity and Reliability the Turkish Version of the Oxford Participation and Activities Questionnaire in Older People
April 28, 2020 updated by: MERV KARAPINAR, Hacettepe University
Validity and Reliability the Turkish Version of the Oxford Participation and Activities Questionnaire (Ox-PAQ) in Older People
To evaluate the validity and reliability of Turkish version of the Oxford Participation and Activities Questionnaire (Ox-PAQ) for Turkish older population.
Following the translation protocol of the Ox-PAQ, Short Form-12, Katz Index of Independence in Activities of Daily Living Scale, The Five Times Sit to Stand Test were administered to 230 older people.
End of this study, occupational therapists, physiotherapists can use the it to assess activity and participation level of older people living in community
Study Overview
Study Type
Observational
Enrollment (Actual)
230
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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Isparta, Turkey
- Suleyman Demirel 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
65 years and older (OLDER_ADULT)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Older people (65 and older years)
Description
Inclusion Criteria:
- Aged 65 years or older
- Mini Mental State Examination score greater than 24,
- Able to mobilize independently.
Exclusion Criteria:
- Severe vision and hearing loss
- Having an orthopaedic, vestibular, neurological or mental problem
- Failure to cooperation
- Presence of an acute disease during recovery.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Ox-PAQ
Time Frame: One year
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It contains 23 items, each measured on a five-point Likert scale.
Each of the 23 items is scored in the same direction (0=Never, 1=Rarely, 2=Sometimes, 3=Often, 4=Always).
Also, Ox-PAQ consist of three domains, Routine Activities (14 items: nos.
1,2,3,4,5,6,7,8,9,10, 13,14,16,17), Social Engagement (4 items: nos.
11,12,15,18) and Emotional Well-Being (5 items: nos.
19,20,21,22,23).
Raw scores of Ox-PAQ are transformed to a range from 0 to 100.
The formula for scoring each dimension is as follows: sum of scores of each question in dimension/ ((4 x number of questions in dimension) x 100) (10).
Higher scores reflect greater problems with activity and participation.
|
One year
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: MERVE KARAPINAR, Suleyman Demirel University, Department of Physiotherapy and Rehabilitation
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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)
January 10, 2018
Primary Completion (ACTUAL)
June 10, 2019
Study Completion (ACTUAL)
June 20, 2019
Study Registration Dates
First Submitted
April 26, 2020
First Submitted That Met QC Criteria
April 28, 2020
First Posted (ACTUAL)
April 30, 2020
Study Record Updates
Last Update Posted (ACTUAL)
April 30, 2020
Last Update Submitted That Met QC Criteria
April 28, 2020
Last Verified
April 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- 191
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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