Get-Ready App to Monitoring Obesity Patients Before and After Bariatric Surgery
Get-Ready: an App for Monitoring Patients With Obesity Before and After Bariatric Surgery. Benefits for Patients and Clinical Team
- Obesity
At a glance
- Phase
- Phase not stated
- Study type
- Interventional
- Sponsor
- Fondazione Policlinico Universitario Campus Bio-Medico
- Enrolment target
- 500
- Started
- 1 February 2026
- Main results due
- 1 September 2029
- Study sites
- 1
- Registry updated
- 24 September 2026
Can you take part?
- Ages 18 years to 65 years.
- Open to any sex.
- You need the condition being studied — healthy volunteers are not accepted.
These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.
Read the full eligibility criteria
Inclusion Criteria: * Patients affected by morbid obesity and eligible for bariatric surgery according to SICOB guidelines (aged between 18 and 65 years, inclusive; body mass index \> 35 kg/m² with obesity-related comorbidities or BMI \> 40 kg/m²) Exclusion Criteria: * Inability or difficulty in using smartphone or PC applications
What this study is about
In the sponsor’s own words, from the registry.
The study aims to evaluate whether the use of Get Ready improves remote patient monitoring, streamlines the different phases of the patient pathway, optimizes healthcare resources by reducing the number of outpatient visits and surgical procedures cancelled due to communication difficulties, and leads to an improvement in the quality of work of the healthcare staff involved
Study sites(1)
Fondazione Policlinico Universitario Campus Bio Medico di Roma
Rome, RM, Italy
Recruiting
Showing 1 of 1 sites. 1 of the 1 site on this study is recruiting right now — a site can stop enrolling while the study as a whole is still open.
Source: ClinicalTrials.gov record NCT07839624. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.
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