Actively Recruiting
Time-restricted Eating and Cognition
Led by German Institute of Human Nutrition · Updated on 2024-07-18
35
Participants Needed
1
Research Sites
41 weeks
Total Duration
On this page
Sponsors
G
German Institute of Human Nutrition
Lead Sponsor
P
Prof. Dr. Olga Ramich (German Institute of Human Nutrition)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study aims to investigate how time-restricted eating (TRE), more specifically TRE at different times (early vs late in the day), influences brain activity, behavior, decision-making, food intake, physical activity, the gut microbiome and metabolic processes. The study intervention procedure is a replication of that described in Peters et al. (2021).
CONDITIONS
Official Title
Time-restricted Eating and Cognition
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Right-handed
- Legally competent
- Physically and mentally healthy
- Body Mass Index (BMI) between 19 and 35 kg/m²
- Fluent in reading and speaking German
You will not qualify if you...
- Weight change greater than 5% of body weight in the last 3 months
- Pregnancy or breastfeeding
- Allergies (inclusion possible after consultation with study doctor)
- History of cardiovascular disease (myocardial infarction, stroke, hypertension, hypotension) in the last year
- Severe psychiatric condition, including drug addiction and depression
- Impaired renal or liver function
- Dementia or other severely debilitating cognitive disease
- History of or current eating disorders (e.g., Bulimia nervosa, Anorexia nervosa, Orthorexia nervosa, Binge-Eating disorder)
- Chronic diseases (e.g., Morbus Crohn, Colitis Ulcerosa)
- Metabolic disorders (e.g., metabolic syndrome, diabetes type 1 or 2)
- Hormonal imbalances (e.g., thyroid gland diseases)
- Consuming diseases (e.g., cancer, cachexia) in the last 2 years
- Surgical removal (partial removal) of digestive organs or history of bariatric surgery
- Autoimmune conditions or current infection
- Blood clotting disorders (e.g., haemophilia)
- Severe anemia
- Severe claustrophobia
- Blood donation four weeks prior to study entry
- Use of oral glucocorticoid therapy
- Use of anticoagulant medication (inclusion possible if medication can be paused)
- Taking medications that require regular eating
- Any medications or supplements known to affect sleep, circadian rhythms, immune activity, or metabolism
- Taking weight loss, lipid, or glucose-lowering medications (e.g., metformin)
- Pacemaker or other electrical implant
- Vaccination during the study or in the two weeks prior
- Immunosuppressive premedication
- Currently on a diet or fasting regime (or within 1 month)
- Professional athletes
- Nicotine consumption
- Drug abuse
- Alcohol consumption exceeding 14 beers (0.3l), wine (0.125l), sparkling wine (0.1l), or schnaps (4cl) per week
- Shift work
- Poor sleep quality (PSQI score greater than 10 at medical screening)
- Travel across more than one time zone one month before or during the study
- Non-removable metallic implants
- Fear of blood draw
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
German Institute of Human Nutrition (DIfE)
Nuthetal, Germany
Actively Recruiting
Research Team
L
Lara Ryan
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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