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NCT Number: NCT06302803

Modified Intermittent Eating on Weight Loss (INTEREST-3 Trial)

Calorie restriction (CR) is the most important treatment for weighting loss. In recent years, two novel types of intermittent fasting recently have gained more attention: the 5:2 diet and time-restricted eating (TRE). TRE requires individuals to eat in a specified number of hours per day (typically 4 to 10 hours) without energy intake restriction. The 5:2 diet involves 5 feast days and 2 fast days per week; participants eat ad libitum without restriction on feast days while 25% of energy needs (approximately 500-800 kcal per day) are consumed on fast days. However, the effects of dietary strategy of intermittent fasting plus time-restricted eating (modified time-restricted eating: TRE 5 days and fasting 2days per week) on weight loss and cardiometabolic risk factors in obese adults have not been proved. This randomized controlled trial aimed to evaluate the effect of modified time-restricted eating (mTRE) and CR on weight loss and cardiometabolic risk factors in obese adults compared to usual health care over 12 months.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Nanfang Hospital of Southern Medical University

Guangzhou, Guangdong, 510515, China

Location status: Recruiting

Location contact

Huijie Zhang, MD,PhD

CONTACT

About this study

Obesity is becoming a major global public health issue. Calorie restriction (CR) is the most important treatment for weighting loss. In recent years, two novel types of intermittent fasting recently have gained more attention: the 5:2 diet and time-restricted eating (TRE). TRE requires individuals to eat in a specified number of hours per day (typically 4 to 10 hours) without energy intake restriction. The 5:2 diet involves 5 feast days and 2 fast days per week; participants eat ad libitum without restriction on feast days while 25% of energy needs (approximately 500-800 kcal per day) are consumed on fast days. However, the effects of dietary strategy of intermittent fasting plus time-restricted eating (modified time-restricted eating: TRE 5 days and fasting 2days per week) on weight loss and cardiometabolic risk factors in obese adults have not been proved. This randomized controlled trial aimed to evaluate the effect of modified time-restricted eating (mTRE) and CR on weight loss and cardiometabolic risk factors in obese adults compared to usual health care over 12 months.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Man or women aged 18-75 years;
  • Body mass index (BMI)of 28.0 to 45.0 kg/m2;

Exclusion criteria

  • History of HIV, hepatitis B or C (self-report) or active pulmonary tuberculosis;
  • Diagnosis of type 1 and type 2 diabetes;
  • History of malignant tumors;
  • Serious liver dysfunction or chronic kidney disease (AST or ALT > 3 times the upper limit of normal, or eGFR<30 ml/min/1.73 m2);
  • History of serious cardiovascular or cerebrovascular disease (angina, myocardial infarction or stroke) in the past 6 months;
  • History of severe gastrointestinal diseases or gastrointestinal surgery in the past 12 months;
  • History of Cushing's syndrome, hypothyroidism, acromegaly, hypothalamic obesity;
  • Being a smoker or having been a smoker in the 3 months prior to their screening visit;
  • Taking medications affecting weight or energy intake/energy expenditure in the last 6 months, including weight loss medications, antipsychotic drugs or other medications as determined by the study physician;
  • Currently participating in weight loss programs or weight change in the past 3 months (> 5% current body weight) ;
  • Women who are pregnant or plan to become pregnant;
  • Patients who cannot be followed for 24 months (due to a health situation or migration);
  • Patients who are unwilling or unable to give informed consent.

Treatment and study plan

Intermittent fasting plus time-restricted eating

Behavioral

Participants in the mTRE group will be instructed to eat during a window of 8 h (8 am to 4 pm) 5 days and fast (approximately 500-600 kcal per day) 2 days per week.

Other names: mTRE

Calorie Restriction

Behavioral

Participants will follow receive a diet of 1500-1800kcal/d for men and 1200-1500kcal/d for women, without restriction on eating time.

Other names: CR

Primary outcomes

  1. Change in body weight over 12 months

    Time frame: Baseline to months 12

    Change in body weight over 12 months

Secondary outcomes

  1. Change in body mass index (BMI)

    Time frame: Baseline to months 12

    body mass index : the weight in kilograms divided by the square of the height in meters.The higher scores mean a worse outcome.

  2. Change in waist circumference

    Time frame: Baseline to months 12

    Wrap a tape measure around the waist at the level of the navel.

  3. Change in body fat composition meassured by DEXA

    Time frame: Baseline to months 12

    Body composition is meassured by dual-energy X-ray absorptiometry scans

  4. Change in liver fat

    Time frame: Baseline to months 12

    Liver fat is assessed by liver Fibroscan

  5. Change in systolic blood pressure

    Time frame: Baseline to months 12

    blood pressure

  6. Change in diastolic blood pressure

    Time frame: Baseline to months 12

    blood pressure

  7. Change in concentration of serum triglyceride

    Time frame: Baseline to months 12

    the contents of serum triglyceride

  8. Change in concentration of serum total cholesterol

    Time frame: Baseline to months 12

    the contents of serum total cholesterol

  9. Change in concentration of serum LDL-c

    Time frame: Baseline to months 12

    the contents of Low Density Lipoprotein

  10. Change in concentration of HbA1c

    Time frame: Baseline to months 12

    the contents of Glycated hemoglobin

  11. Change in insulin sensitivity

    Time frame: Baseline to months 12

    Insulin sensitivity is assessed by HOMA-IR (Homeostatic Model Assessment for Insulin Resistance).

  12. Change in β cell function

    Time frame: Baseline to months 12

    β cell function is assessed by HOMA-B

  13. Change in arterial stiffness measured by pulse wave velocity

    Time frame: Baseline to months 12

    arterial stiffness is measured by pulse wave velocity (PWV)

  14. Change in depression score measured by the Patient Health Questionnaire-9

    Time frame: Baseline to months 12

    Depression is measured by the Patient Health Questionnaire-9 (PHQ-9). The maximum value is 27, and the minimum value is 0 . The higher scores mean a worse outcome.

  15. Change in quality of sleep score measured by the Pittsburgh sleep quality index

    Time frame: Baseline to months 12

    Quality of sleep is measured by the Pittsburgh sleep quality index (PSQI). The maximum value is 21, and the minimum value is 0 . The higher scores mean a worse outcome.

  16. Change in quality of life score measured by the 12-item Short-Form Health Survey Questionnaire

    Time frame: Baseline to months 12

    Quality of life is measured by the 12-item Short-Form Health Survey Questionnaire (SF-12). The maximum value is 100, and the minimum value is 0 . The higher scores mean a better outcome.

Study contacts

Contact information is provided by the study sponsor or research team.

Huijie Zhang, MD. PhD.

CONTACT

[email protected]

+86-020-61641635

Sponsors and collaborators

Lead sponsor

Nanfang Hospital, Southern Medical University

Other

Registry information

Official study title

Effects of Modified Intermittent Eating Strategy on Weight Loss and Cardiometabolic Risk Factors in Obese Adults: a Randomized Clinical Trial

Acronym: INTEREST-3

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Mar 12, 2024
Registry last updated
Jun 24, 2024

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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