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More info
You can access this
clinical trial
if you have
Weight Loss
and you are
between 18 and 30
years old
-
The phase for this study is not defined.
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The purpose

Participants will complete a one-month intervention where they are will restrict their daily food intake to an 8-hour time period, i.e., between 1200 to 2000 hours. During the remaining 16-hour intermittent fasting period (2000 to 1200 hours) participants will be allowed to drink zero calorie beverages (diet soda pop, black coffee, tea, water, etc) in order to maintain normal hydration. There will be no attempt to restrict food intake. Rather simply to restrict the time period each day when food is consumed. Participants' body mass, fat mass, and non-fat mass will be monitored non-invasively using a weigh scale and densitometry via air displacement (Bod Pod) at 0, 2 and 4 weeks following the dietary intervention. Also, participants will be interviewed following the final body composition measure to assess whether or not they continued to follow the intermittent fasting approach.

Provided treatments

  • Behavioral: Time restricted feeding

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT02629900. The sponsor of the trial is University of Western Ontario, Canada and it is looking for 16 volunteers for the current phase.
Official trial title:
The Effect of Time Restricted Feeding on Fat Mass in Overweight Women