- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06794437
Turkish Version of Mobile Device Proficiency Questionnaire
Turkish Version of Mobile Device Proficiency Questionnaire, Validity and Reliability Study
Study Overview
Detailed Description
Information and Communication Technologies (ICT) enable users to perform various tasks with minimal effort. Today, many elderly individuals also own their own mobile devices. Mobile devices are small, lightweight and portable information terminals, and are indispensable for ICT use in our daily lives with models such as smartphones and tablet computers. In addition, in the USA and Japan, 61% and 74.2% of individuals aged 65 and over use smartphones, respectively. Mobile devices are used for various functions in daily life such as making phone calls, messaging, checking programs, shopping, paying bills and accessing entertainment content, facilitating many tasks. However, some elderly individuals who own mobile devices do not sufficiently benefit from the advantages offered by ICT. There are significant differences in internet literacy among elderly individuals, and social and socioeconomic factors can affect the digital gap among elderly individuals. Due to these social factors, efforts to eliminate digital inequality need to be increased in the future.
This study aims to adapt the Mobile Device Proficiency Questionnaires (MDPQ) to Turkish. MDPQ can serve as a basic and quantitative indicator of ICT proficiency among the elderly population. In this context, the Turkish version of MDPQ, MDPQ-T, will be created and its reliability and validity will be verified. We expect this new assessment tool to have the same high reliability and validity as the original version in the Turkish population. We also predict that the duration or frequency of use of mobile devices will be positively correlated with mobile device proficiency measured by MDPQ-T. In addition, we expect not only the accessibility of mobile devices but also the subjective importance, performance and satisfaction level of mobile device use in daily life to be positively correlated with MDPQ-T.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Nilüfer
-
Bursa, Nilüfer, Turkey, 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 or writing problems,
- Having a mobile device such as a phone or tablet,
- 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
|
|
education level of the patients
Time Frame: 1 week
|
education level will be recorded
|
1 week
|
|
Mobile Device Proficiency Questionnaire
Time Frame: 1 week
|
Mobile Device Proficiency Questionnaire will be filled out under the supervision of a physiotherapist
|
1 week
|
|
system usability scale Questionnaire
Time Frame: 1 week
|
system usability scale Questionnaire will 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
- 2025/1-4
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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