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Effects of resistance training and animal protein intake on diet?induced weight loss in obese older women displaying metabolic abnormalities

Completed
Conditions
Obesity, menopause, metabolic syndrome, physical capacity.
Nutritional, Metabolic, Endocrine
Obesity
Registration Number
ISRCTN51723391
Lead Sponsor
niversity of Sherbrooke (Canada)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Female
Target Recruitment
100
Inclusion Criteria

1. Women will be included in the study if they had stopped menstruating for more than 1 yr, and if they have follicle stimulating hormone (FSH) levels > 30 U/L
2. Aged between 60 and 75 years old
3. Body mass index (BMI) between 27 and 40 kg/m2
4. Sedentary (< 2 times a week of exercise)
5. Non-smokers
6. Low to moderate alcohol consumers (< 2 drinks/week)
7. Displaying at least one of the following factor of the metabolic syndrome accordingly to the Adult Treatment Panel III (ATP III?s) definition [63] [triglycerides > 1.70 mmol/L; high density lipoprotein (HDL)-cholesterol < 1.29 mmol/L; resting blood pressure < 160/95 mmHg (treated or not); fasting plasma glucose > 6.1 mmol/L], 7) stable medication(s) for the metabolic syndrome since 6 weeks and
8. Glycated haemoglobin (HbA1c) < 8%

Exclusion Criteria

1. More than three medications for high blood pressure
2. Cardiovascular disease and peripheral vascular disease within 3 months
3. Stroke within 3 months and/or causing inability to complete the exercice program
4. Diabetes treated with insulin
5. Cancer within 5 years (excepted skin and thyroid cancer)
6. Severe hypertension (resting blood pressure > 160/95 mmHg under stable treatement)
7. Total cholesterol > 8 mmol/L
8. Triglycerides >10 mmol/L
9. Low density lipoprotein (LDL)-chol > 4 mmol/L
9. Body weight fluctuation > 3 kg in the previous six months
10. Pituitary disease
11. Renal insufficiency (creatine <45 ml/min)
12. Orthopaedic problems causing inability to complete the exercice program
13. Protein intake <0.8 g/kg or >1.2 g/kg body mass per day

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Dual energy X-ray absorptiometry (DXA) technology to measure total fat mass, bone mass and lean body mass as well as each tissue by region (trunk, legs and arms). <br>2. Other measures of body composition include weight, height, waist and hip circumferences. They are taken before, during and after the intervention (total of 3 times for DXA outcomes and 8 times for other body composition measurements).
Secondary Outcome Measures
NameTimeMethod
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