Turkish Version of Telehealth Usability Questionnaire (TUQ)

NCT04802512 | Completed

• 1 other identifier: HatayMustafaKU
• Study Type: observational
• Target: 170
• Locations: 1 country
• Sites: 2

Brief Summary

The Telehealth Usability Questionnaire (TUQ) was developed to evaluate the usability of telehealth applications and services. The Turkish validity and reliability study of the scale, originally in English, has not been conducted before. The aim of this study is to develop the Turkish version of the Telehealth Usability Questionnaire (TUQ), which is a new stability tool, and to report its reliability assessment.

Conditions

Health Care Acceptor; Health Knowledge, Attitudes, Practice; Patient Participation

Outcome Measures

Primary Outcomes (1)

• Reliability and Validity of TUQ by Correlation Analysis.

  with telehealth will be researched

  12 month

Study Arms (2)

patients

patients who were used telehealth

Procedure: validity and reability study

health professional

health professional who were used telehealth.

Procedure: validity and reability study

Interventions

validity and reability study PROCEDURE

validity and reliability assessment of the Turkish version of the Telehealth Usability Questionnaire (TUQ)

health professional; patients

Eligibility Criteria

• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

The Turkish validity and reliability of the scale, which was created to evaluate the usability of the telehealth service for service users (patients) and providers (health professional), will be investigated.

You may qualify if:

• Participants will undergo screening to confirm eligibility, completion of initial screening form, and MMSE evaluation. Study subjects were enrolled with MMSE scores between 29-30, inclusive (healthy/control), 25-28, inclusive (mild cognitive impairment), and 10-24 (dementia).

You may not qualify if:

• Unable to complete computerized and standard pencil-and-paper based assessments

Sponsors & Collaborators

• Irem Hüzmeli: lead

Study Sites (2)

Hatay Mustafa Kemal University

Hatay, Merkez, 31010, Turkey (Türkiye)

Location

Online

Hatay, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Patient Acceptance of Health Care; Behavior; Patient Participation

Condition Hierarchy (Ancestors)

Treatment Adherence and Compliance; Health Behavior

Study Officials

• Irem Huzmeli, Phd

  Mustafa Kemal University

  STUDY DIRECTOR

• Esra Dogru Huzmeli, Assoc Prof.

  Mustafa Kemal University

  PRINCIPAL INVESTIGATOR

• Mehmet Karadağ, Asist. Prof.

  Mustafa Kemal University

  STUDY CHAIR

Study Design

• Study Type: observational
• Observational Model: CASE ONLY
• Time Perspective: CROSS SECTIONAL
• Target Duration: 15 Days
• Sponsor Type: OTHER
• Responsible Party: SPONSOR INVESTIGATOR
• PI Title: Phd lecturer

Study Record Dates

• First Submitted: March 14, 2021
• First Posted: March 17, 2021
• Study Start: March 12, 2021
• Primary Completion: June 12, 2022
• Study Completion: June 12, 2022
• Last Updated: December 5, 2023

Record last verified: 2023-12

Locations

TU (2)