Skip to content

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.

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.

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07297342
Enrollment
200
Registered
2025-12-22
Start date
2025-04-02
Completion date
2027-06-30
Last updated
2025-12-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus ( Type 1 and Type 2), Hypertension, Obesity &Amp; Overweight, Obstructive Sleep Apnea (OSAS)

Keywords

Get Ready, application, bariatric, compliance

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.

Interventions

OTHERGetReady application

Postoperative application usage

OTHERIntensified GetReady application

Postoperative application usage

Sponsors

Medtronic
CollaboratorINDUSTRY
Sint Dimpna Ziekenhuis Geel
Lead SponsorNETWORK

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients undergoing bariatric surgery

Exclusion criteria

* Previous bariatric surgery

Design outcomes

Primary

MeasureTime frameDescription
Weight3monts, 6 months, 12 monthsOverall weight, in kg's
Rand-36 Health Survey12monthsHealth survey, score 0-100 with higher score indicating better health.
Bloodwork6 months and 12 monthsDeficiencys in blood results
Sigstad score3months, 6 months and 122 monthsclassifying dumping symptoms, score \>7 sugests dumping, score \<-4 suggests other disease.

Secondary

MeasureTime frameDescription
N° of unplanned clinical visits12monthsN° of unplanned clinical visits

Countries

Belgium

Contacts

Primary ContactRuben Vanlommel, Doctor
ruben.vanlommel@ziekenhuisgeel.be014577777

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026