Multimodal METformin and FINGER Lifestyle Intervention to Prevent Cognitive Impairment and Disability in Older Adults at Risk for Dementia: a Phase IIb Multi-national Randomised, Controlled Trial

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Other, Combination product
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Dementia is the main cause of disability in older adults, currently affecting about 50 million people world-wide with this number estimated to triple in the next 30 years. In MET-FINGER, we aim to understand whether the FINGER 2.0 multidomain intervention, combining healthy lifestyle changes and a drug for diabetes (metformin), may help reduce the risk of dementia and improve health and independence among older adults. The study primary objective is to test the effect of the intervention, compared to healthy lifestyle advice, on the change in cognition, measured as a composite score including 14 of neuropsychological/cognitive tests. The secondary objective is to test the intervention effect on change in individual cognitive domains, functioning level, and risk factors for dementia (e.g., lifestyle, medical, and psychosocial). To this aim, a range of personal/health-related data and blood samples, will be collected. Potential interactions between metformin and lifestyle changes; potential disease-modifying effects; and feasibility of the metformin + lifestyle combination will be explored. 600 older people with risk factors for dementia, but without dementia/substantial cognitive impairment, will be recruited in the United Kingdom, Finland, and Sweden (at least 50% with higher genetic risk of Alzheimer's Disease/dementia based on the Apolipoprotein E (APOE) gene). Participants will be randomly assigned 1:1 to either a self-guided multidomain lifestyle intervention or to the FINGER 2.0 multidomain lifestyle-based intervention. Outcome assessors will be blinded to group allocation. Within the FINGER 2.0 intervention group, participants at increased risk of diabetes, will be randomly assigned 1:1:1 to either the metformin 2000mg/day, metformin 1000mg/day, or placebo group (double blinded). The intervention duration is 24 months. The lifestyle intervention includes four main components: physical exercise, diet, brain training and health checks. In the self-guided group, participants will create their own program, based on health advice and recommendations which will be provided during the study. In the FINGER 2.0 intervention group, participants will receive intensive lifestyle guidance, and participate in structured activities, which will be as tailored as possible on each person's daily habits and needs. Over the 2-year study period, all participants will attend four assessment visits: baseline, 6-, 12-, and 24-months.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 60
Maximum Age: 79
Healthy Volunteers: t
View:

• Main inclusion criteria (all participants)

‣ Age 60-79 years.

⁃ Cardiovascular Risk Factors, Aging and Dementia (CAIDE) Risk Score ≥6 points.

⁃ Cognitive performance at the mean level or slightly lower than expected for age according to local population norms based on the Montreal Cognitive Assessment (MoCA) test and the Consortium to Establish a Registry for Alzheimer's Disease (CERAD) verbal learning test.

⁃ Proficiency in the local language (English, Finnish or Swedish)

• Inclusion criteria for metformin/placebo treatment (only for participants in the FINGER 2.0 multimodal lifestyle-based intervention arm)

‣ No diagnosed diabetes or known contraindications to metformin treatment.

⁃ Elevated adiposity (BMI≥25 kg/m2 OR waist circumference \> 102 cm in men and \> 88 cm in women) OR mildly impaired fasting glucose (6.1-6.9 mmol/l).

Locations
Other Locations
Finland
Finnish Institute of Health and Welfare - THL
RECRUITING
Helsinki
Sweden
Karolinska Institutet
RECRUITING
Solna
United Kingdom
Ageing Epidemiology Research Unit, Imperial College London
RECRUITING
London
Contact Information
Primary
Miia Kivipelto, MD, PhD
miia.kivipelto@ki.se
+46(0)739940922
Backup
Alina Solomon, MD, PhD
alina.solomon@uef.fi
+358(0)403552015
Time Frame
Start Date: 2023-01-25
Estimated Completion Date: 2027-06-28
Participants
Target number of participants: 600
Treatments
Sham_comparator: Self-guided multidomain lifestyle intervention
In this group, participants will build their own healthy lifestyle program based on standard healthy lifestyle advice that they will receive at individual consultations with the study physician/nurse as part of the study visits, covering four main components (diet, physical activity, cognitive training, and cardiovascular/metabolic risk monitoring). The intervention duration is 2 years.
Active_comparator: FINGER 2.0 multidomain lifestyle-based intervention
Within this group, participants will receive a structured intensive lifestyle intervention through individual consultations and group meeting sessions. Four main lifestyle components will be included (diet, physical activity, cognitive training, and cardiovascular/metabolic risk monitoring) as well as social interaction through the group meetings/sessions.~In this group, participants eligible for metformin treatment will be further randomised to either:~* 2000mg/day~* 1000mg/day~* placebo.~Metformin and placebo will be dispensed every 3 months, both administered orally. The intervention duration is 2 years
Related Therapeutic Areas
Sponsors
Collaborators: Alzheimer's Association, Karolinska Institutet, Alzheimerfonden, Fingers Brain Health Institute, Karolinska University Hospital, Finnish Institute for Health and Welfare, Region Stockholm, Merck KGaA, Darmstadt, Germany, Alzheimer's Drug Discovery Foundation
Leads: Imperial College London

This content was sourced from clinicaltrials.gov