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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05871710
Other study ID # TelePulm
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date August 1, 2023
Est. completion date March 1, 2024

Study information

Verified date May 2023
Source Uskudar State Hospital
Contact Mustafa H Temel, M.D.
Phone +905342714872
Email mhuseyintemel@gmail.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The objective of this research is to translate the Tele-Pulmonary Rehabilitation Acceptance Scale into Turkish and assess its reliability and accuracy.


Description:

The use of telehealth in pulmonary rehabilitation, also known as telerehabilitation, is a novel approach in healthcare practice. In order to effectively implement telerehabilitation programs, it is important to evaluate how potential users perceive and accept this new type of program. Thus, the aim of this research was to create a measuring tool that could assess the level of acceptance of telerehabilitation among healthcare providers and patients. A group of experts in pulmonary rehabilitation, telehealth, information technology, and scale development have reviewed and confirmed the content validity of the Tele-Pulmonary Rehabilitation Acceptance Scale. This scale is significant because it offers a consistent means of collecting data to measure the level of acceptance towards telerehabilitation among potential users. This study aims to translate and show the consistency and validity of the Tele-Pulmonary Rehabilitation Acceptance Scale in Turkish.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date March 1, 2024
Est. primary completion date December 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Being a patient in need of pulmonary rehabilitation or a healthcare professional working in the field of pulmonary rehabilitation. - Being a native Turkish speaker. - Giving consent to participate in the study. Exclusion Criteria: - Any disease or condition that prevents reading, understanding, or filling out forms. - Not giving consent to participate in the study.

Study Design


Intervention

Other:
Turkish version of the Tele-Pulmonary Rehabilitation Acceptance Scale
The Tele-Pulmonary Rehabilitation Acceptance Scale is a measuring tool that assesses the level of acceptance towards telerehabilitation programs among healthcare providers and patients in the field of pulmonary rehabilitation. It is used to evaluate the attitudes, beliefs, and perceptions of potential users towards telerehabilitation, which is a form of healthcare delivery that utilizes telecommunication technology to provide remote rehabilitation services to patients. The scale is intended to provide a standardized data collection tool that can be used to measure the level of acceptance of telerehabilitation programs among different groups of potential users. This scale will be translated into Turkish by a researcher who has an advanced level of knowledge in English and whose native language is Turkish.
Scale Evaluation Form
The healthcare providers and the patients will be asked about their opinions on the scale's construction, usefulness, and scope using a 100 mm visual analog scale.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Uskudar State Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Validity and reliability of the Turkish version of the Tele-Pulmonary Rehabilitation Acceptance Scale The primary outcome is the overall validity and reliability of the Turkish version of the Tele-Pulmonary Rehabilitation Acceptance Scale. This scale is a Likert scale with a total of 13 questions and the score for each question ranges from 1 to 4. The total score is 52 and higher scores indicate that the patient is more inclined to adopt telerehabilitation. This will involve analyzing the responses of participants to the questionnaire to determine if it accurately measures the intended construct. The study will also assess the internal consistency of the responses to determine if the scale produces consistent results when administered multiple times to the same group of patients. 1 day
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