๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-06-26

Time-restricted Eating, Window Timing, Type 2 Diabetes Status and Sex on Glycemic Control (NCT06118931)

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

๐ŸŸข Recruiting Observational / Diagnostic ๐Ÿง  Behavioral & Psychological Program Sponsor: University of Toronto

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

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.

Who can join: Review the eligibility criteria below.

Location: Remote Ontario-wide โ€” Toronto, Ontario

Age range: 40 Years

๐Ÿงช Interventions in This Study

  • Early (7:00 - 16:00) TRE (BEHAVIORAL)
  • Mid (9:30 - 18:30) TRE (BEHAVIORAL)
  • Late (12:00 - 21:00) TRE (BEHAVIORAL)

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (1 Sites)

  • Remote Ontario-wide โ€” Toronto, Ontario

๐Ÿ“ž Contact the Study Coordinator

Phone: (416) 946-4069

Email: amy.kirkham@utoronto.ca

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—