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Completed

NCT Number: NCT05730231

Clinical Trials of Effects of Time Restricted Eating on Health Parameters in Adults

In a randomized controlled trial we will research the effect of calorie restriction with early and mid-day time-restricted eating (TRE) and daily calorie restriction on weight loss and human health parameters. Participants will be divided into three groups: early time-restriction group (8:00 AM to 4:00 PM), mid-day restriction group (1:00 PM to 9:00 PM) and daily calorie restriction group (8:00 AM to 9:00 PM). Participants will follow dietary strategy with three planned meals and calorie restriction. Anthropometrical and biochemical parameters will be measured at baseline, after one month, two months and at after three months of intervention. Resting metabolic rate, ultrasound scan of abdomen and ultrasound scan of carotid arteries will be measured at baseline and after three months of intervention. In addition, stool samples will be also taken at baseline and after three months of intervention.

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Key information

About this study

Obesity has become one of the world's most common diseases and is a major global public health challenge. Obesity contributes to an increased risk of developing various chronic diseases, such as diabetes, metabolic syndrome, hypertension, cardiovascular and kidney diseases and many others. Reducing excess body weight and improving eating habits decreases risk of disease and mortality. A lot of dietary strategies for weight loss are known and most of them are based on daily calorie restriction. Recently, an increasingly popular dietary strategy has been "time restricted eating (TRE)". In this strategy, all calorie intake is restricted within a consistent interval of less than 12 hours (4 - 10 hours). Eating window is limited to early part of the day - early TRE or mid-day TRE. Research shows that TRE has a number of beneficial effect on individuals, including weight loss, improvement of insulin sensitivity, hypercholesterolaemia, circadian rhythm of hormone secretion and other. Which TRE (early or mid-day TRE) has better health effects is still being investigated. It is also not clear how the timing, number and composition of individual meals affect on the health indicators, mentioned previously.

Therefore, the aim of our study is to evaluate and compare the effects of calorie restriction with early and mid-day time-restricted eating (TRE) and daily calorie restriction on weight loss and human health parameters in adults with at least two components of metabolic syndrome and yet not receiving any medication. The components of metabolic syndrome (lipid profile, blood pressure, anthropometry, inflammation status, glucose levels), antioxidative status, hormones (leptin, ghrelin, cortisol, insulin, adiponectin, cholecystokinin, melatonin, BDNF, IGF-1) will be measured. In addition changes in gene expression of different proteins will be examined. Moreover, stool samples will be also taken at baseline and after three months of intervention.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • BMI 25-35 kg/m2

+ one of the following criteria:

  • Increased waist circumference ≥ 94 cm in men and ≥ 80 cm in women
  • Fasting plasma glucose > 5,6 mmol/L
  • Elevated fasting plasma triglycerides 1,7 mmol/l
  • Reduced high-density lipoprotein (HDL)-cholesterol < 1,0 mmol/l for men, < 1,3 mmol/l for women
  • Elevated blood pressure, systolic blood pressure > 130 mm Hg and diastolic blood pressure > 85 mm Hg
  • Without medicals for hypertension and hypercholesterolemia
  • Morning or afternoon working time

Exclusion criteria

  • Pregnant or plan to be become pregnant
  • Lactating women
  • Active smoking
  • Diagnosis of diabetes
  • Eating disorders
  • Currently enrolled in a weight-management program
  • Uncontrolled medical condition due to gastrointestinal, psychiatric, rheumatologic, oncologic, hematologic or endocrine diseases
  • History of tumor
  • History of serious cardiovascular or cerebrovascular diseases
  • Taking medicines that may affect weight and appetite

Treatment and study plan

Effects of calorie restriction and time-restricted eating on human health

Other

Calorie restriction plan will be prepared for each participant. After nutritional data collection at baseline, all participant will attend educational sessions about healthy diet and beneficial effects of time-restricted eating. To estimate total energy needs, individuals' RMR will be measured from indirect calorimeter and multiplied by the appropriate factor of physical activity (from 1.3 to 1.6), and then a reduction of 200-500 kcal will be made. Macronutrient composition of the diet will be approximately 45-55% of carbohydrate, 30-35% of fat, and 15-20% of protein. 30% of daily energy intake will be consumed by breakfast, 40% by lunch and 30% by dinner. During posting participants will be allowed to consume only water and herbal infusions without added sugars or sweeteners. Dietary intake of participants will be followed during the study using a 24-h recall. Dietary data will be analysed using the Open Platform for Clinical Nutrition accessible through the website http://opkp.si/.

Primary outcomes

  1. Change in Body Weight

    Time frame: three months

    Changes in body weight (in kilograms) from baseline to week twelve measured with bioelectrical impedance analysis (BIA) Tanita MC-980MA

Secondary outcomes

  1. Change in Body Fat

    Time frame: three months

    Changes in percentage of body fat from baseline to week twelve measured with bioelectrical impedance analysis (BIA) Tanita MC-980MA

  2. Changes in Visceral Fat Rating

    Time frame: three months

    Changes in visceral fat rating (index) from baseline to week twelve measured with bioelectrical impedance analysis (BIA) Tanita MC-980MA. The range of the visceral fat rating (scale) is from 0 to 30. Higher scores indicate excess visceral fat (a worse outcome).

  3. Changes in Muscle mass

    Time frame: three months

    Changes in muscle mass (in kilograms) from baseline to week twelve measured with bioelectrical impedance analysis (BIA) Tanita MC-980MA

  4. LDL Cholesterol

    Time frame: three months

    Changes in LDL cholesterol measured by biochemical analyzer Cobass

  5. Inflammation

    Time frame: three months

    Changes in C-reactive protein levels measured by biochemical analyzer Cobass

  6. Glucose levels

    Time frame: three months

    Changes in glucose levels measured by biochemical analyzer Cobass

  7. Resting metabolic rate

    Time frame: three months

    Changes in resting metabolic rate measured by (MedGem® Microlife, Medical Home Solutions, Inc., Golden, CO)

  8. ultrasound scan of abdomen

    Time frame: three months

    ultrasound scan of abdomen measured by Resona 7 Mindray

  9. ultrasound scan of carotid arteries

    Time frame: three months

    ultrasound scan of carotid arteries measured by Resona 7 Mindray

  10. Antioxidative potential

    Time frame: three months

    Antioxidative potential will be determined with DPPH radical measurement.

  11. Blood Pressure

    Time frame: three months

    Changes in systolic blood pressure measured by blood pressure device (Omron M3)

Sponsors and collaborators

Lead sponsor

University of Primorska

Other

Registry information

Official study title

Comparison of Calorie Restriction With Early Time-restricted Eating and Calorie Restriction With Mid-day Time-restricted Eating and Daily Calorie Restriction

Acronym: TRE

Important dates

Study start
2023
Primary completion
2023
Study completion
2024
First posted
Feb 15, 2023
Registry last updated
Mar 5, 2025

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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