Obesity
Conditions
Interventions
This is a randomized controlled clinical trial with two parallel arms, 1:1 allocation, non-blinded, lasting 12 weeks, designed to evaluate the effect of a structured home-based exercise program in wom
Sponsors
Escola bahiana de medicina e saúde pública - FBDC
Escola bahiana de medicina e saúde pública - FBDC
Eligibility
Sex/Gender
Female
Age
40 Years to 59 Years
Inclusion criteria
Inclusion criteria: Women aged between 40 and 59 years; with a Body Mass Index (BMI) = 30 kg/m²
Exclusion criteria
Exclusion criteria: Use of medications for the treatment of obesity; Medical conditions that prevent the safe performance of physical exercise; Women who are already enrolled in training programs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| A reduction in body weight is expected after 12 weeks of intervention, verified by weighing on a standardized digital scale, considering a minimum decrease of 5% of the initial weight between the pre- and post-intervention assessments as a clinically relevant change. | — |
Secondary
| Measure | Time frame |
|---|---|
| The primary outcome of the study will be the absolute change in body weight (kg) from baseline to 12 weeks of intervention. Secondary outcomes will include changes in Body Mass Index (kg/m²), body fat percentage assessed by bioimpedance, and quality of life score measured by a validated instrument, all analyzed from baseline to 12 weeks of follow-up | — |
Countries
Brazil
Contacts
Public ContactComitê em Pesquisa
Escola bahiana de medicina e saúde pública - FBDC
Outcome results
None listed