Turkish Version of Mobile Device Proficiency Questionnaire

April 11, 2025 updated by: Selim Mahmut GÜNAY, Uludag University

Turkish Version of Mobile Device Proficiency Questionnaire, Validity and Reliability Study

The Mobile Device Proficiency Questionnaire (MDPQ) contains 46 questions with eight subscales, which are as follows: mobile device basics, communication, data and file storage, internet, calendar, entertainment, privacy, and troubleshooting and software management. Each question item is rated on a five-point scale based on the individual's subjective proficiency level. The scores ranged from 8 to 40 and were scored in a similar manner to in the original version. For each subscale of the MDPQ, responses for all questions were averaged. These averaged scores were then summed across subscales to come up with a total score of the MDPQ.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

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

Observational

Enrollment (Actual)

305

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

    • Nilüfer
      • Bursa, Nilüfer, Turkey, 16210
        • Uludag University

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

  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

Geriatric individuals between the ages of 65-80

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

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
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

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Selim Mahmut GÜNAY, Dr, Uludag University

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 27, 2025

Primary Completion (Actual)

March 14, 2025

Study Completion (Actual)

March 14, 2025

Study Registration Dates

First Submitted

January 20, 2025

First Submitted That Met QC Criteria

January 20, 2025

First Posted (Actual)

January 27, 2025

Study Record Updates

Last Update Posted (Actual)

April 16, 2025

Last Update Submitted That Met QC Criteria

April 11, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 2025/1-4

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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