- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06794463
Turkish Version of Computer Usage Proficiency Questionnaire
Turkish Version of Computer Usage Proficiency Questionnaire, Validity and Reliability Study
Study Overview
Status
Conditions
Detailed Description
The adaptation of the elderly population to technology has increased rapidly with demographic changes and developments in the field of Gerontechnology, which supports successful aging by integrating technology into the daily lives of older individuals. Gerontechnology focuses on the development and application of communication and information technologies in order to increase the independence and social participation of older individuals.
Digital competence requires cognitive and technical skills that include processes such as finding, understanding, evaluating, creating and communicating digital information; it is of fundamental importance for the digital society. The Computer Use Competence Survey stands out as an assessment tool that measures the competence of older individuals in using computers and information technologies. This survey supports digital inclusion by contributing to the development of training programs tailored to individual needs. In addition, the Computer Use Competence Survey can be used as a continuous assessment tool to measure the progress of individuals participating in digital inclusion programs over time. Another strength of the Computer Use Competence Survey is that it can identify specific barriers that older individuals encounter when using digital technology and allows for special measures to be taken to overcome these barriers.
The aim of this study is to provide a reliable tool for assessing the digital competence of the elderly population in Turkey by performing the cross-cultural adaptation and content validation of the Computer Use Proficiency Questionnaire in Turkish.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
nilüfer
-
Bursa, nilüfer, Turkey (Türkiye), 16210
- Uludag University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Being a native Turkish speaker,
- Having no reading and writing problems,
- Having a desktop or laptop computer,
- Agreeing to participate in the study
Exclusion Criteria:
-Individuals with neurological diseases such as cognitive impairment, Alzheimer's, dementia, etc. will be excluded from the study.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Age of the patients
Time Frame: 1 week
|
Age will be recorded.
|
1 week
|
|
Gender of the patients
Time Frame: 1 week
|
Gender will be recorded.
|
1 week
|
|
Computer Usage Proficiency Questionnaire
Time Frame: 1 week
|
Computer Usage Proficiency Questionnaire will be filled out under the supervision of a physiotherapist
|
1 week
|
|
System Usability Scale
Time Frame: 1 week
|
System Usability Scalewill be filled out under the supervision of a physiotherapist
|
1 week
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Selim Mahmut GÜNAY, Dr, Uludag University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2025/1-5
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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