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临床试验/NCT06118931
NCT06118931招募中不适用

The Impact of Time-restricted Eating, Window Timing, Type 2 Diabetes Status and Sex on Glycemic Control

University of Toronto1 个研究点 分布在 1 个国家目标入组 123 人开始时间: 2025年6月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
123
试验地点
1
主要终点
Average 24-hour glucose total area under the curve (AUC) over 7 days

研究概览

简要总结

This study will evaluate the effectiveness of time-restricted eating (TRE), which is a form of intermittent fasting. When performing TRE, individuals consume all of their calories within a specific time window and then only consume water or other no calorie drinks the rest of the day. TRE is performed each day. There is no restriction on the quality or amount of food that people can consume during their eating window (ad libitum eating) with TRE, which can last anywhere from 4 to 12 hours. We are comparing three different 9-hour eating windows to determine whether the start and stop time of the eating window impact blood sugar control in individuals with obesity who also have or are at risk for type 2 diabetes. We also aim to determine if there are differences in the effects of the timing of eating window between males and females.

详细描述

The overarching aim of this study is to evaluate the interactions between TRE window timing, type 2 diabetes status, and sex among individuals with obesity. The first objective is to compare the effects of three 9-h TRE window times (early: 7:00-16:00 h, mid: 9:30-18:30 h, delayed: 12:00-21:00 h) on real-time, free-living glycemic control. The second objective is to determine if type 2 diabetes status (type 2 diabetes versus prediabetes or moderate+ risk for type 2 diabetes aka at risk for type 2 diabetes) modifies the effect of eating window timing on glycemic control outcomes. The exploratory objectives include: 1) determine whether sex modifies TRE adherence or the effect of TRE on metabolic changes relative to control; and 2) to compare changes in dietary intake, body weight, and blood pressure within and between early, mid, and delayed TRE. We have the following hypotheses related to these objectives:

  1. The early TRE window will result in the most favourable glycemic control outcomes but also the lowest participant acceptability followed by mid and delayed TRE.
  2. There will be larger differences in glycemic control outcomes between the TRE window timings among those with type 2 diabetes compared to those at risk for type 2 diabetes.
  3. TRE adherence and changes in glycemic control, and weight loss with all TRE window times (relative to control) will be higher in men vs women.
  4. Energy, carbohydrate, and sugar intake, body weight, and blood pressure will decrease during TRE, but with no differences by window timing.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

年龄范围
40 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Aged 40 years or older
  • Body mass index <50 kg/m2
  • Have access to an Apple or Android cellphone with Bluetooth.
  • Have type 2 diabetes or be at risk for type 2 diabetes (defined as self-report of pre-diabetes, a recent (within 12 months) measure of HbA1c between 5.7 and 6.4%, waist circumference (WC) that is BMI specific; for women: BMI >= 18.5-24.9, WC >= 80cm; BMI >= 25-29.9, WC >= 90cm; BMI >= 30-34.9, WC >= 105cm; BMI >= 35+, WC >= 115cm; for men: BMI >= 18.5-24.9, WC >= 90cm; BMI >= 25-29.9, WC >= 100cm; BMI >= 30-34.9, WC >= 110cm; BMI >= 35+, WC >= 125cm.

排除标准

  • Individuals with type 2 diabetes will be excluded if: (1) currently on >2 monotherapies for diabetes, (2) have had diabetes therapy medication or dosage changes <3 months, (3) self-reported hemoglobin A1c >9.0%, (4) taking exogenous insulin, or (5) taking sulfonylureas
  • The following exclusion criteria applies to all potential participants:
  • History of or referral for bariatric surgery
  • Weight loss >3% in the last 3 months
  • Taking antiobesity (weight loss) medications
  • Body weight >390lbs
  • Diagnosed with severe cognitive disorder that precludes them from giving consent
  • Inability or unwillingness to change their eating window to follow those prescribed in the study
  • Currently consistently eating during <11.5 hour period .
  • Physician-diagnosed eating disorder
  • Having a pacemaker or receiving dialysis.
  • Not having access to a Lifelabs location.

研究组 & 干预措施

Early (7:00-16:00h) TRE

Experimental

Participants will be asked to eat ad libitum between the hours of 7:00 - 16:00 each day for seven days, and then only drink water or other no calorie beverages for the rest of the day. On the 8th day, they will consume one meal replacement beverage at 7:00 and be instructed to not consume anything else for two hours. After the two hours they will be instructed to return to their normal baseline eating habits.

干预措施: Early (7:00 - 16:00) TRE (Behavioral)

Mid (9:30-18:30h) TRE

Experimental

Participants will be asked to eat ad libitum between the hours of 9:30 - 18:30 each day for seven days, and then only drink water or other no calorie beverages for the rest of the day. On the 8th day, they will consume one meal replacement beverage at 9:30 and be instructed to not consume anything else for two hours. After the two hours they will be instructed to return to their normal baseline eating habits.

干预措施: Mid (9:30 - 18:30) TRE (Behavioral)

Late (12:00-21:00h) TRE

Experimental

Participants will be asked to eat ad libitum between the hours of 12:00 - 21:00 each day for seven days, and then only drink water or other no calorie beverages for the rest of the day. On the 8th day, they will consume one meal replacement beverage at 12:00 and be instructed to not consume anything else for two hours. After the two hours they will be instructed to return to their normal baseline eating habits.

干预措施: Late (12:00 - 21:00) TRE (Behavioral)

Control

No Intervention

During the first week of the study, participants will be asked to eat as they normally do, and to not make any changes regarding when they are stopping or starting eating.

结局指标

主要结局

Average 24-hour glucose total area under the curve (AUC) over 7 days

时间窗: 7 days

Assessed for 7 continuous days using a continuous glucose monitor.

次要结局

  • TRE fasting window adherence(7 days)
  • Average daily nocturnal glucose over 7 evenings(7 days)
  • Postprandial glucose(2 hours)
  • Glycemic viability(7 days)
  • Patient acceptability(7 days)
  • Average 24-hour glucose over 7 days(7 days)
  • Average daily time spent in hyperglycemia over 7 days(7 days)
  • TRE fasting duration adherence(7 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Amy Kirkham

Principal Investigator

University of Toronto

研究点 (1)

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