Obesity Clinical Trial
Official title:
Effects of Weight Loss Management on Cognitive Function in Elderly Obese Women
According to studies, the risk of cerebrovascular disease and cognitive decline are associated with age-related changes. In addition, there is data suggesting a relationship between the progression of this pathology and the presence of obesity and associated metabolic disorders. According to to some research, weight loss associated with cognitive function decline. In this regard, the development of effective, applicable in real clinical practice methods of non-drug treatment and prevention of cerebrovascular disorders and age-related cognitive decline in people with obesity and metabolic disorders, who are at high risk, seems to be extremely relevant. The main goal of the study is to compare the effectiveness of various weight loss approaches and to study their effects on the cognitive functions of elderly obesity women.
Status | Recruiting |
Enrollment | 200 |
Est. completion date | December 30, 2023 |
Est. primary completion date | June 30, 2023 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 60 Years to 75 Years |
Eligibility | Inclusion Criteria: 1. Female; 2. Age 60 and over; 3. BMI 30.0 kg/m2 or more. Exclusion Criteria: 1. Male; 2. age under 60; 3. BMI <30.0 kg/m2; 4. 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; 5. less than 6 months after suffering cardiovascular events, stroke, severe surgical interventions and injuries; 6. alcohol abuse (including chronic pancreatitis of alcoholic etiology) or drug addiction at present or within the last 5 years; 7. history of malignant diseases, regardless of the treatment during the last 5 years; 8. less than 4 weeks after suffering acute infectious and / or inflammatory diseases, after the onset of complete clinical and laboratory remission; 9. pregnancy and lactation; 10. history of allergic reactions to components of the study product and/or placebo or intolerance to components of the study product and/or placebo. |
Country | Name | City | State |
---|---|---|---|
Russian Federation | Nutrition Clinic of the Federal Research Centre of Nutrition, Biotechnology and Food Safety | Moscow |
Lead Sponsor | Collaborator |
---|---|
Federal State Budgetary Scientific Institution "Federal Research Centre of Nutrition, Biotechnology | Federal Stare Budgetary Scientific Institution, Mental Health Research Center |
Russian Federation,
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* Note: There are 17 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from baseline body weight at 12 weeks | The dynamics of body weight | Baseline (visit 1) and after 12 weeks (visit 2) | |
Primary | Change from baseline Montreal Cognitive Assessment (MoCa) test scores at 12 weeks | The changes in the cognitive testing results | Baseline (visit 1) and after 12 weeks (visit 2) | |
Primary | Change from baseline Trail Making Test (TMT) a&b test scores at 12 weeks | The changes in the cognitive testing results (normal range - less than 78 and 273 seconds (=scores)). | Baseline (visit 1) and after 12 weeks (visit 2) | |
Primary | Change from baseline Word recall test scores at 12 weeks | The changes in the cognitive testing results (normal range as 45 words (=scores) and more out of 5 repetitions). Minimal - 0 (worse result), maximal score - 50 (excellent result). | Baseline (visit 1) and after 12 weeks (visit 2) | |
Primary | Change from baseline Mean response time in the test "Schulte tables" at 12 weeks | The changes in the cognitive testing results | Baseline (visit 1) and after 12 weeks (visit 2) | |
Primary | Change from baseline The Stroop Color and Word Test results at 12 weeks | The changes in the cognitive testing results | Baseline (visit 1) and after 12 weeks (visit 2) | |
Primary | Change from baseline Verbal fluency test results at 12 weeks | The changes in the cognitive testing results | Baseline (visit 1) and after 12 weeks (visit 2) | |
Secondary | Change from baseline fat mass at 12 weeks | The changes in the fat mass according to the bioimpedance analysis | Baseline (visit 1) and after 12 weeks (visit 2) | |
Secondary | Change from baseline skeletal muscle mass at 12 weeks | The changes in the skeletal muscle mass according to the bioimpedance analysis | Baseline (visit 1) and after 12 weeks (visit 2) | |
Secondary | Change from baseline visceral fat at 12 weeks | The changes in visceral fat according to the bioimpedance analysis | Baseline (visit 1) and after 12 weeks (visit 2) | |
Secondary | Change from baseline total cholesterol serum levels at 12 weeks | The changes of total cholesterol serum levels | Baseline (visit 1) and after 12 weeks (visit 2) | |
Secondary | Change from baseline LDL-cholesterol serum levels at 12 weeks | The changes of LDL-cholesterol serum levels | Baseline (visit 1) and after 12 weeks (visit 2) | |
Secondary | Change from baseline HOMA-IR (homeostasis model assessment - insulin resistance) index at 12 weeks | The changes of HOMA-IR index | Baseline (visit 1) and after 12 weeks (visit 2) | |
Secondary | Change from baseline C-reactive protein (CRP) serum levels at 12 weeks | The changes of CRP serum levels | Baseline (visit 1) and after 12 weeks (visit 2) | |
Secondary | Change from baseline Tumor Necrosis Factor Alpha (TNFa) serum levels at 12 weeks | The changes of TNFa serum levels | Baseline (visit 1) and after 12 weeks (visit 2) | |
Secondary | Change from baseline systolic blood pressure (SBP) at 12 weeks | The changes of SBP | Baseline (visit 1) and after 12 weeks (visit 2) | |
Secondary | Change from baseline diastolic blood pressure (DBP) at 12 weeks | The changes of DBP | Baseline (visit 1) and after 12 weeks (visit 2) | |
Secondary | Change from baseline grip strength at 12 weeks | The changes of grip strength measured by grip dynamometer on the leading hand | Baseline (visit 1) and after 12 weeks (visit 2) | |
Secondary | Change from baseline Six Minute Walk Test distance at 12 weeks | The changes of Six Minute Walk Test results | Baseline (visit 1) and after 12 weeks (visit 2) | |
Secondary | Change from baseline Hamilton Anxiety Rating Scale at 12 weeks | The changes of Hamilton Anxiety Rating Scale results (normal range - 6 scores and less). | Baseline (visit 1) and after 12 weeks (visit 2) | |
Secondary | Change from baseline Hamilton Depression Rating Scale at 12 weeks | The changes of Hamilton Depression Rating Scale results (normal range - 7 scores and less). | Baseline (visit 1) and after 12 weeks (visit 2) |
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