Insulin Resistance Syndrome Metabolic Syndrome Syndrome X
Conditions
Interventions
During the study, subjects will receive daily (in the morning) 5.7 g NWT*03 or
placebo powders for 36 weeks.
Sponsors
Universiteit Maastricht
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: - Men and women, aged between 60-75 years - Subjective cognitive decline (SCD) - BMI between 25-35 kg/m2 - Fasting plasma glucose
Exclusion criteria
Exclusion criteria: - Left-handedness - Current smoker, or smoking cessation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoints are the difference in brain vascular function and cognitive performance between interventions. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints are effects on insulin-sensitivity and peripheral vascular function. | — |
Countries
Netherlands
Outcome results
None listed