Effects of Weight Loss Management on Cognitive Function in Elderly Women With Obesity
Obesity, Cognitive Change
About this trial
This is an interventional other trial for Obesity focused on measuring Elderly, Obesity, Weight loss, Cognitive Change, Exogenous Ketones, Diet, Physical activity
Eligibility Criteria
Inclusion Criteria: Female; Age 60 and over; BMI 30.0 kg/m2 or more. Exclusion Criteria: Male; age under 60; BMI <30.0 kg/m2; patients unable or unwilling to comply with the requirements of the protocol, including the signing of informed consent (inability to give such consent due to mental deficiency or language barrier), as well as non-compliance with the schedule of visits, persons unable to independently make a decision and sign an informed consent; less than 6 months after suffering cardiovascular events, stroke, severe surgical interventions and injuries; alcohol abuse (including chronic pancreatitis of alcoholic etiology) or drug addiction at present or within the last 5 years; history of malignant diseases, regardless of the treatment during the last 5 years; less than 4 weeks after suffering acute infectious and / or inflammatory diseases, after the onset of complete clinical and laboratory remission; pregnancy and lactation; history of allergic reactions to components of the study product and/or placebo or intolerance to components of the study product and/or placebo.
Sites / Locations
- Nutrition Clinic of the Federal Research Centre of Nutrition, Biotechnology and Food SafetyRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Experimental
Active Comparator
Placebo Comparator
Active Comparator
No Intervention
The Product Group
The Combined Intervention Group
The Placebo Group
The Diet Group
The Control Group
The Product group is prescribed with the investigated product - exogeneous ketone bodies.
The Combined Intervention Group is prescribed with the investigated product -in combination with regular physical trainings.
The Placebo Group is prescribed with the Placebo.
The Diet Group is prescribed with the Diet designed with 500 kcal reduction from daily energy expenditure.
The Control Group is prescribed with standard recommendations for weight loss.