- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04802499
Turkish Version of Telehealth Satisfaction Survey (TeSS)
December 2, 2023 updated by: Irem Hüzmeli, Mustafa Kemal University
Investigation of the Validity and Reliability of the Turkish Version of Telehealth Satisfaction Survey (TeSS)
The Turkish validity and reliability of the scale, which was created to evaluate the satisfaction of individuals, caregivers, and coordinator providing telerehabilitation services within the scope of telehealth, will be investigated.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
The telehealth satisfaction survey (TeSS) has been developed according to expectations, taking into account a device previously used in telehealth studies in Saskatchewan.
The scale was initially used as part of a national study to evaluate the use of telehealth practices in improving professional access by residents of isolated Northern First Nations communities.The scale designed for telehealth services has been developed in English.
Validity and reliability studies have been carried out by being translated into various languages.
The Turkish validity and reliability study of the scale, originally in English, has not been conducted before.
Study Type
Observational
Enrollment (Actual)
150
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
-
-
Merkez
-
Hatay, Merkez, Turkey, 31010
- Hatay Mustafa Kemal 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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
telehealth patients caregivers and health professionals who practice telehealth
Description
Inclusion Criteria:
- Men and woman who used telehealth
Exclusion Criteria:
- Individuals who have the poor cooperation Mini-Mental State Exam scores of under 23
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
persons who using telehealth (patients)
patients who have received telehealth
|
Translation and cultural adaptation of the scale will be designed according to the appropriate procedure.
Turkish data will be uploaded in the online online method.
The scale will be communicated online to those who have received telerehabilitation services, caregivers and healthcare professionals who have applied it.
The reliability of the questionnaire will be made by test-retest and internal consistency analysis.
Volunteers will be asked to answer the questionnaire online after 5 days.
After two weeks, the participants will be asked to answer the questionnaire again with the same method online with 5 days intervals.
After all data are collected, validity analysis will be performed
|
|
caregivers
family member of the patients who recieved telehealth
|
Translation and cultural adaptation of the scale will be designed according to the appropriate procedure.
Turkish data will be uploaded in the online online method.
The scale will be communicated online to those who have received telerehabilitation services, caregivers and healthcare professionals who have applied it.
The reliability of the questionnaire will be made by test-retest and internal consistency analysis.
Volunteers will be asked to answer the questionnaire online after 5 days.
After two weeks, the participants will be asked to answer the questionnaire again with the same method online with 5 days intervals.
After all data are collected, validity analysis will be performed
|
|
health professions
persons who use the telehealth.
|
Translation and cultural adaptation of the scale will be designed according to the appropriate procedure.
Turkish data will be uploaded in the online online method.
The scale will be communicated online to those who have received telerehabilitation services, caregivers and healthcare professionals who have applied it.
The reliability of the questionnaire will be made by test-retest and internal consistency analysis.
Volunteers will be asked to answer the questionnaire online after 5 days.
After two weeks, the participants will be asked to answer the questionnaire again with the same method online with 5 days intervals.
After all data are collected, validity analysis will be performed
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Turkish Reliability and Validity of TESS (telehealth Satisfaction Survey) for patients, caregivers and health professional who use telehealth
Time Frame: March 2021-April 2022
|
validation and reliability of survey in Turkish
|
March 2021-April 2022
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Irem Huzmeli, PhD, Mustafa Kemal 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)
March 12, 2021
Primary Completion (Actual)
May 12, 2022
Study Completion (Actual)
June 12, 2022
Study Registration Dates
First Submitted
March 14, 2021
First Submitted That Met QC Criteria
March 14, 2021
First Posted (Actual)
March 17, 2021
Study Record Updates
Last Update Posted (Actual)
December 5, 2023
Last Update Submitted That Met QC Criteria
December 2, 2023
Last Verified
December 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- HatayMKU
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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