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Nutritional intervention, based on the Brazilian Cardioprotective Diet, with a physical exercise program, both in online format, to control health parameters in people in the late postoperative period stomach reduction surgery

Online multicomponent intervention, based on the Brazilian Cardioprotective Diet and a resistance training program, to control metabolic parameters in late postoperative period of Bariatric Surgery: a randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-4pdv53d
Enrollment
Unknown
Registered
2023-12-08
Start date
2023-04-03
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

obesity and sarcopenia.

Interventions

Open-label, randomized, controlled clinical trial. A total of 125 people who meet the eligibility criteria will be randomly allocated into 2 distinct groups. Both researchers and participants will kno
2) What are ultra-processed foods and what are the reasons for avoiding them
3) Importance of eating carefully, in an appropriate environment and accompanied, when possible
4) Which foods should be avoided because they increase cardiovascular risk (cholesterol, saturated fat and sodium)
5) Importance of the presence of foods that contain cardioprotective nutrients (antioxidants and dietary fiber), with a focus on fruits, vegetables, legumes, milk and dairy products. The physical exer

Sponsors

Faculdade de Ciências da Saúde da Universidade de Brasília
Lead Sponsor
Faculdade de Ciências da Saúde da Universidade de Brasília
Collaborator

Eligibility

Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Adults who are physically inactive; age between 18 and 60 years; both sexes; submitted to bariatric surgery for more than 5 years, by the Unified Health System (SUS) or in private clinics; residents of the Federal District

Exclusion criteria

Exclusion criteria: Individuals who are physically active through the performance of any type of regular and/or programmed vigorous physical exercise; who presents any decompensated chronic illness or any evident illness that prevents from exercising; pregnant women; women who are breastfeeding; individuals who have psychiatric disorders in the use of psychotropic drugs; who use a pacemaker; in use of hormone therapy or on medication for weight loss; those who have any type of amputation; who do not have access to a cell phone or computer

Design outcomes

Primary

MeasureTime frame
To evaluate the effect of the multicomponent intervention on sarcopenic obesity markers evaluated according to the consensus on sarcopenic obesity developed by the European Society for Clinical Nutrition and Metabolism (ESPEN) and the European Association for the Study of Obesity (EASO). The markers will be the force of palmar pressure, through the dynamometer; a body composition, measured by the dual-energy x-ray absorptiometry technique; functionality and muscle strength through testicles such as sit and stand, timed up and go (TUG), and a five-minute walk. It is expected that after 12 weeks of multicomponent intervention, there will be a significant improvement (p<0.05) in muscle strength and function, verified through the improvement of performance in functional tests and body composition, with a reduction in body weight, an increase in the percentage of fat-free mass, and reduction of the percentage of adipose tissue

Secondary

MeasureTime frame
Evaluate the effect of the multicomponent intervention on the participant's global health. Global health will be assessed using office blood pressure, biochemical markers (plasma concentrations of glucose, insulin, glycated hemoglobin, blood count, lipogram), liver function (concentrations of oxaloacetate transaminase and glutamic pyruvic transaminase), markers of renal function (urea serum creatinine, glomerular filtration rate), sleep quality, using the Pittsburgh Sleep Quality Index, and resting energy expenditure, using indirect calorimetry. The usual food consumption will be evaluated, through the application of a 24-hour recall, and the quality of the diet, through the application of the ultra-processed food consumption tracking instrument, applied in the Risk and Protective Factors Surveillance System for Chronic Diseases by Telephone Inquiry (VIGITEL). Eating behavior and body image perception will be evaluated through the application of validated questionnaires, the Three Factor Eating Questionnaire (TFEQ), and the Body Appreciation Scale (BAS), respectively. It is expected that after 12 weeks of multicomponent intervention, there will be a significant improvement (p<0.05) in health markers, through the improvement of biochemical markers, and sleep quality; food consumption, by increasing the amount and frequency of in unprocessed and minimally processed foods with low caloric density, and reducing the consumption of ultra-processed foods with high caloric density; and improvement of eating behavior, by reducing scores related to emotional eating, dismayed eating, uncontrolled eating, and increased conscious eating and body appreciation

Countries

Brazil

Contacts

Public ContactKênia Mara De Carvalho

Universidade de Brasília

kenia@unb.br+55-61-31071747

Outcome results

None listed

Source: REBEC (via WHO ICTRP)