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Completed

NCT Number: NCT06022094

Effect of a Two-month Carbohydrate-restricted Diet on Energy Metabolism in a Seniors' Residence

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.

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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Research Center on Aging

Sherbrooke, Quebec, J1H 4C4, Canada

About this study

Finding an effective therapeutic strategy for Alzheimer's disease (AD) is a societal priority, but it also remains a major challenge. With one exception in 2021, no new pharmaceutical treatment for AD has been approved for over 20 years. However, several clinical trials demonstrate the potential of ketogenic interventions to restore brain energy and improve cognition in people with mild cognitive impairment and AD. Recently, the largest and longest clinical trial of its kind shows that compensating for energy deficit in the brain during aging improves brain metabolic and cognitive functioning in people with early AD and could potentially delay AD.

One of the main types of ketogenic intervention is the highly reduced carbohydrate (5-10% of daily energy value compared to a normal value of 50-65%) and very high fat ketogenic diet. Despite the now well-established safety of the ketogenic diet and its therapeutic value in the treatment of epilepsy and type 2 diabetes, the latter remains difficult to implement in because of the compliance challenge. A reduced glycemic load diet where intake of refined carbohydrates and added sugar is restricted is found to be much less restrictive than a ketogenic diet. Phase 1 of this project showed that decreased carbohydrate (sugar) intake may improve long-term glycemic control and compliance compared to more severe carbohydrate restriction. Having better blood glucose control may also be important in decreasing the risk of AD possibly by improving the metabolic profile and/or by promoting the production and use of ketones. However, its effectiveness in helping cognition in the elderly is still unknown and any changes in dietary habits can be addressed with some resistance.

The objective of this project is therefore to answer the following question: does a reduction in carbohydrates of 30 to 50% for 2 months reduce the risk of AD by improving the metabolic profile in people living in a senior residence?

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

2 months of reduced carb menus

Other

Participants will eat a reduced carb menu for 2 months

Other names: R-CHO

Primary outcomes

  1. Change in blood glucose levels

    Time frame: 2 months

    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. Change in blood ketones levels

    Time frame: 2 months

    Blood ketones will be measured before/after the intervention in people in a senior residence via blood sampling.

  3. Change in blood insulin levels

    Time frame: 2 months

    Blood insulin will be measured before/after the intervention in people in a senior residence via blood sampling.

Secondary outcomes

  1. Change in blood triglycerides levels,

    Time frame: 2 months

    Blood triglycerides levels will be measured before/after the intervention in people in a senior residence via blood sampling.

  2. Change in blood cholesterol levels

    Time frame: 2 months

    Blood cholesterol levels will be measured before/after the intervention in people in a senior residence via blood sampling.

  3. Change in blood glycated hemoglobin levels

    Time frame: 2 months

    Blood glycated hemoglobin levels will be measured before/after the intervention in people in a senior residence via blood sampling.

Sponsors and collaborators

Lead sponsor

Université de Sherbrooke

Other

Registry information

Official study title

Effect of a Two-month Carbohydrate-restricted Diet on Energy Metabolism in a Seniors' Residence: The SAGE Study

Acronym: SAGE

Important dates

Study start
2023
Primary completion
2023
Study completion
2024
First posted
Sep 1, 2023
Registry last updated
Jun 3, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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