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LevantAE! APP: reducing sedentary lifestyle in obese patients before bariatric surgery

Reducing sedentary time in Obese individuals pre-bariatric surgery at a teaching hospital: using the “Levantae! App”

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-10zh7737
Enrollment
Unknown
Registered
2024-09-17
Start date
2024-09-20
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

sedentary behavior

Interventions

This is a randomized controlled clinical trial involving 90 patients who are candidates for bariatric surgery, who will be randomly assigned to three groups, all with similar characteristics, such as

Sponsors

Centro de Ciências da Saúde
Lead Sponsor
Hospital das Clínicas da Universidade Federal de Pernambuco
Collaborator

Eligibility

Age
18 Years to 59 Years

Inclusion criteria

Inclusion criteria: Men and women; aged 18 years or older up to 59 years old; body mass index = 30kg/m2; not participating in any physical exercise program; being properly monitored at the general surgery outpatient clinic of the Hospital das Clínicas of the Federal University of Pernambuco; being able to understand and use the application; having their own smartphone with a data package capable of installing the application; residing in the metropolitan region of Recife

Exclusion criteria

Exclusion criteria: Have contraindications for practicing physical activities; patients with severe arthritis, fibromyalgia or any other type of disease that prevents them from performing any type of physical activity; do not use the application for at least 70% of the stipulated period

Design outcomes

Primary

MeasureTime frame
Effectiveness of the application in reducing time spent in sedentary behavior in individuals with morbid obesity

Secondary

MeasureTime frame
The reduction in daily sedentary time, measured in minutes, over three months, comparing the three groups (intervention, placebo and control)

Countries

Brazil

Contacts

Public ContactAndre Costa

Universidade Federal de Pernambuco

andre.santoscosta@ufpe.br+55 (81) 2126.8000

Outcome results

None listed

Source: REBEC (via WHO ICTRP)