Actively Recruiting
Time-restricted Eating Study (TRES): Impacts on Anthropometric, Cardiometabolic and Cardiovascular Health
Led by Universiti Teknologi Mara · Updated on 2024-07-18
48
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
Sponsors
U
Universiti Teknologi Mara
Lead Sponsor
M
Ministry of Higher Education, Malaysia
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn about the effects of time-restricted eating in patients with history of acute coronary syndrome. The main questions it aims to answer are: 1) Is 10-hr TRE safe and feasible for patients with ACS; 2)What are the impacts of 10-hr TRE on anthropometric measurements, cardiometabolic health and cardiovascular health compared to ad libitum eating in patients with ACS?. Participants will be asked to limit eating duration to 10 hours daily.
CONDITIONS
Official Title
Time-restricted Eating Study (TRES): Impacts on Anthropometric, Cardiometabolic and Cardiovascular Health
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 to 65 years
- History of acute coronary syndrome (ACS)
- Clinically stable condition
- Self-reported daily eating window of at least 12 hours
You will not qualify if you...
- Severe obesity (BMI ≥ 40 kg/m²)
- Unstable weight in past 3 months (gain or loss over 4 kg)
- Unstable cardiovascular, renal, cardiac, liver, lung, adrenal, or nervous system disease
- Use of medications or supplements affecting sleep, circadian rhythms, or metabolism
- Pregnant or lactating women
- Working overnight shifts more than one day per week
- Regular fasting over 15 hours/day or recent frequent 24-hour fasts
- Active tobacco or illicit drug use or history of alcohol abuse treatment
- Type I diabetes or insulin-treated diabetes
- Use of anti-obesity or weight-affecting drugs
- Enrollment in weight loss or management programs including surgery
- Severe kidney failure (GFR <30 mL/min)
- Eating disorder or uncontrolled psychiatric illness
- Active malignancy treatment
- History of gastrointestinal surgery or impaired nutrient absorption
- Recent or planned travel crossing more than two time zones
- Participation in other interventional studies
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Pusat Perkhidmatan Klinikal (CTC) UiTM
Kuala Selangor, Malaysia
Actively Recruiting
Research Team
M
Mazuin Kamarul Zaman, MMed Sc
CONTACT
N
Nur Islami Mohd Fahmi Teng, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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