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Recruiting NCT07297342

NCT07297342 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.

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Clinical Trial Summary
NCT ID NCT07297342
Status Recruiting
Phase
Sponsor Sint Dimpna Ziekenhuis Geel
Condition Obesity &Amp; Overweight
Study Type INTERVENTIONAL
Enrollment 200 participants
Start Date 2025-04-02
Primary Completion 2026-01-30

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type INTERVENTIONAL
Interventions
GetReady applicationIntensified GetReady application

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 200 participants in total. It began in 2025-04-02 with a primary completion date of 2026-01-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The aim of this study is to assess the impact of a newly intensified digital platform following bariatric surgery. This will be measured using several questionnaires. The following objectives will be evaluated: the exact amount of weight loss achieved preoperatively with the preparatory diet; the occurrence of dumping symptoms; the assessment of quality of life (QOL); and compliance with supplement intake. 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.

Eligibility Criteria

Inclusion Criteria: * Patients undergoing bariatric surgery Exclusion Criteria: * Previous bariatric surgery

Contact & Investigator

Central Contact

Ruben Vanlommel, Doctor

✉ ruben.vanlommel@ziekenhuisgeel.be

📞 014577777

Frequently Asked Questions

Who can join the NCT07297342 clinical trial?

This trial is open to participants of all sexes, studying Obesity &Amp; Overweight. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07297342 currently recruiting?

Yes, NCT07297342 is actively recruiting participants. Contact the research team at ruben.vanlommel@ziekenhuisgeel.be for enrollment information.

Where is the NCT07297342 trial being conducted?

This trial is being conducted at Geel, Belgium.

Who is sponsoring the NCT07297342 clinical trial?

NCT07297342 is sponsored by Sint Dimpna Ziekenhuis Geel. The trial plans to enroll 200 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology