A Prospective Randomnised Controlled Trial Comparing Overall Patient Compliance in a Bariatric Surgical Pathway Using the Standard Versus a More Intensified and Interactive Version of the "Get Ready" Smartphone Application.
NCT ID: NCT07297342
Last Updated: 2025-12-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
200 participants
INTERVENTIONAL
2025-04-02
2027-06-30
Brief Summary
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By examining the impact of an enhanced digital platform, we aim to address critical questions regarding the effectiveness of improved patient support in the digital domain. Moreover, given the increasing prevalence of bariatric surgery as a therapeutic option for obesity, it is of utmost importance to identify strategies to optimize patient education and support through digital tools. This study not only contributes to the scientific understanding of digital support in bariatric care but also has important implications for the further development of the "Get Ready" application, ensuring that it remains at the forefront of providing comprehensive and patient-centered support in the evolving landscape of bariatric surgery.
Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Standard GetReady application group
Standard GetReady application group
GetReady application
Postoperative application usage
Intensified GetReady application
Intensified GetReady application
Intensified GetReady application
Postoperative application usage
Interventions
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GetReady application
Postoperative application usage
Intensified GetReady application
Postoperative application usage
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
ALL
No
Sponsors
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Medtronic
INDUSTRY
Sint Dimpna Ziekenhuis Geel
NETWORK
Responsible Party
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Locations
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Sint Dimpna ziekenhuis
Geel, , Belgium
Countries
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Central Contacts
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Facility Contacts
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Ruben Vanlommel, Doctor
Role: primary
Other Identifiers
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ERP-2023-13530
Identifier Type: -
Identifier Source: org_study_id