Clinical Trials in Brazil / NCT07820774
Starting soon Not applicable

Multimodal Intervention for Weight Management and Health in the Elderly Population

NCT07820774 · tracked via the Priya Life Science Brazil tracker
Sponsor
Universidade Cesumar (UNICESUMAR)
Phase
Not applicable
Started
2026-09-14
Last updated
2026-09-15

Condition(s) studied

Obesity & Overweight

Investigational drug(s) / intervention(s)

Nutritional guidance focused on adopting a high-protein diet.Group Cognitive Behavioral Therapy InterventionResistance Training Program

Nutritional guidance focused on adopting a high-protein diet.: The nutritional guidance will be delivered in a group setting by nutritionist(s), with 16 weekly sessions lasting 25-30 minutes over 16 weeks. The intervention will focus on the sustainable adoption of a high-protein diet based on commonly consumed foods, without providing protein supplements and considering participants' socioeconomic and cultural contexts. The protein target will be 1.2-1.6 g/kg/day, calculated using adjusted body weight and distributed evenly across main meals. Accessible, high-quality protein sources will be prioritized, supported by practical nutrition education strategies such as meal planning, portion guides, and food substitution lists. Adherence will be monitored using 3-day food diaries completed every three weeks. The program will be organized into four progressive modules, ranging from nutrition fundamentals in aging to the consolidation and maintenance of dietary changes.

Group Cognitive Behavioral Therapy Intervention: The Cognitive Behavioral Therapy (CBT) intervention will be delivered weekly in 25-30-minute group sessions, conducted by a trained psychologist for the GBI and GINT groups. The program will focus on promoting sustainable changes in thoughts, emotions, and behaviors related to excess weight. It will be structured into four progressive modules: Foundations and Self-Awareness; Cognitive and Behavioral Skills; Biopsychosocial Integration; and Consolidation and Maintenance. Strategies will include psychoeducation, self-monitoring, goal setting, stimulus control, cognitive restructuring, problem-solving, and relapse prevention. The intervention will specifically address emotional eating, eating disinhibition, and self-efficacy and will be integrated with nutritional guidance and resistance training. Homework assignments and adherence monitoring will be used throughout the intervention.

Resistance Training Program: The resistance training (RT) program will be conducted over 16 weeks, with three sessions per week on non-consecutive days, each lasting approximately 40 minutes and supervised by qualified Physical Education and Physiotherapy professionals. The protocol will include exercises targeting the upper limbs, lower limbs, and trunk, performed in two 1-minute sets, with 45-second rest intervals. Training intensity will be monitored using the OMNI Rating of Perceived Exertion Scale (OMNI-RPE) and progressively adjusted across six phases, starting from very light to light effort, progressing to hard to very hard effort, and ending with a recovery week. Before the intervention, participants will complete familiarization sessions covering the exercises, proper technique, and the perceived exertion scale to ensure safety and reliable monitoring of training intensity.

Study summary

Aging may be accompanied by changes in body composition, muscle strength, metabolic health, and well-being. In older adults with overweight or obesity, strategies that combine physical exercise, behavioral changes, and nutritional guidance may contribute to better health and the maintenance of healthier habits.

This study aims to investigate the effects of a 16-week intervention combining resistance training, group cognitive behavioral therapy, and nutritional guidance for a higher-protein diet. Changes in body composition, muscle strength and function, vascular and metabolic health, cognitive function, psychological outcomes, quality of life, autonomy, self-care, and motivation for exercise and changes in eating habits will be assessed.

The study will include adults aged 60 years or older who have low levels of physical activity and excess body fat. Participants will be randomly assigned to one of three groups. The first group will receive resistance training only; the second group will receive resistance training plus group cognitive behavioral therapy; and the third group will receive resistance training, group cognitive behavioral therapy, and nutritional guidance for a higher-protein diet. This comparison will help determine the effects of each additional component of the intervention.

Resistance training will be performed three times per week. Group cognitive behavioral therapy sessions will be held weekly and will address strategies to support sustainable behavioral changes, including self-awareness, goal setting, the relationship between thoughts, emotions, and behaviors, problem-solving, and maintenance of behavioral changes. Nutritional guidance will also be provided in weekly group sessions, focusing on the sustainable adoption of a higher-protein diet using commonly consumed foods while considering participants' individual circumstances and autonomy.

Assessments will be conducted before and after the 16-week intervention to evaluate potential changes associated with the interventions. Comparing the three groups will help determine whether adding psychological and nutritional strategies to resistance training provides additional benefits for the physical, metabolic, cognitive, and psychological health of older adults with overweight or obesity.

Eligibility

Sex
ALL
Min age
60 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 60 years; * Presence of excess adiposity/overweight or obesity, according to protocol criteria; * Medical clearance to perform supervised physical exercises and the tests; * No regular participation in structured resistance training over the past 5 months. Exclusion Criteria: * Contraindication to resistance training or physical testing; * Unstable or uncontrolled cardiovascular disease; * Recent (\< 6 months) coronary or cerebrovascular event; * Uncontrolled arterial hypertension; * Untreated secondary/endocrine causes of obesity; * Use of medications that significantly alter body mass or composition; * Current use of anti-obesity medication, including GLP-1 agonists; * History of bariatric surgery or scheduled procedure; * Active weight loss process or weight fluctuation \> 5% in the last 6 months.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
UniCesumar - Centro Universitário Cesumar, Maringá, Paraná 87050-900 Maringá Brazil

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07820774 on ClinicalTrials.gov ↗ ← All trials in Brazil