Healthy Aging Clinical Trial
— SAGEOfficial title:
Effect of a Two-month Carbohydrate-restricted Diet on Energy Metabolism in a Seniors' Residence: The SAGE Study
Verified date | May 2024 |
Source | Université de Sherbrooke |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The present study will assess the effects on glucose, ketones and other blood biomarkers fuels, cognition, quality of life, physical activity and well-being of a reduced carbohydrate menu (R-CHO) for 2 months in a population living in a residence for the elderly. This intervention study, identified as the SAGE project (phase 2), follows on from the Ketohome project (phase 1) assessing the feasibility of such a project.
Status | Completed |
Enrollment | 24 |
Est. completion date | May 15, 2024 |
Est. primary completion date | December 15, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 60 Years and older |
Eligibility | Inclusion Criteria: - Senior men or women residing in VÜ resident home; - Understand, read and write French; - Possess sufficient visual and auditory acuity to pass the cognitive tests; - Available during the intervention period Exclusion Criteria: - Body mass index < 20; - T1 diabetic; - Insulin-dependent T2 diabetic; - Mini Mental State Exam (MMSE) < 20; - Weight loss >10% in the last 6 months, involuntary or voluntary; - Known and uncontrolled hypoglycaemia; - Moderate to severe digestive illnesses that may be aggravated by dietary changes; - Severe dysphagia; - Supplementation with medium chain triglycerides oil, ketone salts, ketone ester, adherence to the ketogenic diet, reduced carbohydrate diet, intermittent fasting, or other diet or supplements that may significantly increase ketones in the past month; - Participation in other intervention research projects on nutrition or aimed at metabolic change simultaneously. - Medical condition that could prevent the participant from completing the study according to the doctor's opinion |
Country | Name | City | State |
---|---|---|---|
Canada | Research Center on Aging | Sherbrooke | Quebec |
Lead Sponsor | Collaborator |
---|---|
Université de Sherbrooke |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in blood glucose levels | Blood glucose will be monitored continuously with a real-time continuous glucose monitor (CGM) for two 10-days periods; before/after intervention in people in a senior residence. | 2 months | |
Primary | Change in blood ketones levels | Blood ketones will be measured before/after the intervention in people in a senior residence via blood sampling. | 2 months | |
Primary | Change in blood insulin levels | Blood insulin will be measured before/after the intervention in people in a senior residence via blood sampling. | 2 months | |
Secondary | Change in blood triglycerides levels, | Blood triglycerides levels will be measured before/after the intervention in people in a senior residence via blood sampling. | 2 months | |
Secondary | Change in blood cholesterol levels | Blood cholesterol levels will be measured before/after the intervention in people in a senior residence via blood sampling. | 2 months | |
Secondary | Change in blood glycated hemoglobin levels | Blood glycated hemoglobin levels will be measured before/after the intervention in people in a senior residence via blood sampling. | 2 months |
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