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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05428059
Other study ID # 5312256943
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date August 1, 2022
Est. completion date July 1, 2024

Study information

Verified date August 2023
Source Cukurova University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Obesity, which is the second leading cause of preventable death in the world, affects all the systems in the body and affects many physiological problems, as well as the mental state, body image and quality of life of the individual. For this reason, obese individuals try various treatment methods in order to get rid of obesity, and in cases where these methods fail, they often prefer bariatric surgery. It is very important that patients who will undergo bariatric surgery can adapt to the anatomical changes in their body and shape their lifestyle accordingly. Otherwise, it is inevitable for patients to face various complications after surgery. After bariatric surgery, a structured training program in the preoperative period is of great importance in order for the patient to adapt to the changes in his body, to prevent the development of possible complications, to be affected by the negativities that may occur due to the current change, and to prepare for the new lifestyle. In this context, the main subject of this research is to enable individuals to gain healthy lifestyle behaviors by providing mobile-based training and consultancy services that enable them to easily access the right information at the desired time and place.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 50
Est. completion date July 1, 2024
Est. primary completion date December 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Being literate, - Being able to understand, speak Turkish and not have a hearing impairment, - First time to undergo bariatric surgery, - Absence of any psychiatric disorder that will reduce the ability to comprehend and understand, - Ability to use Android-based smartphones, - Agreeing to participate in the research. Exclusion Criteria: - Patient's desire to quit the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
mobile education
The training content prepared by the researchers will be presented to the expert opinion. After the necessary arrangements, it will be installed on the mobile application. The mobile application will be downloaded to the patients' phones for one month. It will be in live consultation.

Locations

Country Name City State
Turkey Çukurova University Institute of Health Sciences Adana

Sponsors (1)

Lead Sponsor Collaborator
Cukurova University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary The Effect of Mobile Health-Education Application on Healthy Lifestyle Behaviors in Patients Planned for Bariatric Surgery Data will be evaluated using the Healthy Lifestyle Behaviors Scale-II. The minimum score that can be obtained from the 52-item scale is 52, and the maximum score is 208. A high score from the scale indicates that individuals have good HLPS levels, and low scores indicate bad HLBD. one months
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