Intensified Digital Platform for Enhanced Bariatric Surgery Support
This study aims to provide enhanced supportive care through an intensified digital platform for individuals undergoing bariatric surgery.
GetReady application
+ Intensified GetReady application
Treatment Adherence and Compliance+26
+ Apnea
+ Behavior
Supportive Care Study
Summary
Study start date: April 2, 2025
Actual date on which the first participant was enrolled.This study focuses on individuals who have undergone bariatric surgery, a procedure to help with weight loss. The research aims to understand the effects of a newly enhanced digital platform, designed to support patients after their surgery. The goal is to improve patient education and support through digital tools, which is increasingly important as bariatric surgery becomes a more common treatment for obesity. This study could pave the way for better patient-centered support in the field of bariatric care, potentially improving the quality of life for those who have had this surgery. Participants in this study will use an intensified version of the 'Get Ready' smartphone application, designed to provide more interactive support. The study will measure several aspects, including the amount of weight lost before surgery due to a preparatory diet, the occurrence of dumping symptoms, which is a common side effect of bariatric surgery, and the quality of life. Additionally, the study will assess how well participants follow the recommended supplement intake. The results could help in further developing the 'Get Ready' application, ensuring it provides the best possible support for patients in their post-surgery journey.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.200 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria: * Patients undergoing bariatric surgery Exclusion Criteria: * Previous bariatric surgery
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
50% chance of being blinded to the placebo group
Treatment Groups
Group I
PlaceboGroup II
Active ComparatorStudy Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location