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The Effect of Time Restricted Feeding on Fat Mass in Overweight Women

The Effect of Time Restricted Feeding on Fat Mass in Overweight Women

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02629900
Enrollment
16
Registered
2015-12-14
Start date
2016-01-31
Completion date
2016-04-30
Last updated
2016-01-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Weight Loss

Keywords

Weight Loss, Intermittent fasting

Brief summary

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.

Detailed description

Participants (16 overweight women, BMI (Body mass index) ˃25, ages 18- 30 y)will complete a one-month intervention where they 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' fat mass will be monitored non-invasively using densitometry (with a Bod Pod) prior to and following a 4 week intervention where the participants will eat their normal daily intake during an 8-hour period each day (1200 to 2000 hours). The Bod Pod measures body volume via air displacement and together with an accurate measure of body mass enables body density to be calculated (Density = mass/volume). Satisfaction, hunger, and fullness with the diet will be monitored on a weekly basis using a validated visual analog scale (Flit et al, 2000). Adherence to the diet will also be assessed on a weekly basis as the number of days the diet was followed. During the 16-hour fasting period participants will be able to drink as much of zero calorie beverages as they desire. On day 2, 7, 14, 21, & 28 participants will return to the lab at 8am (following a 12 hour fasting period) and both the acidity of their urine (using a urine dip stick) and their blood sugar (using a glucometer) will be tested. Following one month the participants will be allowed either to continue this eating pattern or revert to their prior 3 meal intake. After a month of self-regulation, the participants' fat mass will be measured again using the Bod Pod.

Interventions

BEHAVIORALTime restricted feeding

Participants will consume their daily calories only between 12:00 and 20:00 for 4 weeks

Sponsors

University of Western Ontario, Canada
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Asymptomatic participants between the ages of 18-30 years with body mass index ˃25 will be studied

Exclusion criteria

* Diabetic * Pregnant * Individuals with a history of fainting * Low blood sugar * Heart disease, migranes, or heart burn * Participants less then 18 of age * Anyone who for health or performance reasons should not skip breakfast will be excluded. These will be assessed by self report

Design outcomes

Primary

MeasureTime frameDescription
Fat mass change over 4 weeks period of intervention4 weeksBody fat mass change (%) will be measured using BodPod over the course of 4 weeks at 0, 2 and 4 weeks

Secondary

MeasureTime frameDescription
Urine acidity change over 4 weeks of intervention4 weeksUrine acidity will be measured following a 12 hours fasting at 0800 using a urine dip stick on days 2, 7, 14, 21, & 28
Blood sugar change over 4 weeks of intervention4 weeksFasted blood sugar will be measured following a 12 hours fasting at 0800 using a finger prick glucometer (Free Style Lite) on days 2, 7, 14, 21, & 28
Non-fat mass change over 4 weeks period of intervention4 weeksBody non-fat mass (lean mass) (%) will be measured using BodPod over the course of 4 weeks at 0, 2 and 4 weeks
Feeling of hunger change over 4 weeks of intervention4 weeksHunger will be monitored on a weekly basis using a validated visual analog scale (Flit et al, 2000)
Feeling of fullness change over 4 weeks of intervention4 weeksFeeling of fullness will be monitored on a weekly basis using a validated visual analog scale (Flit et al, 2000)
Diet satisfaction change over 4 weeks of intervention4 weeksDiet satisfaction will be monitored on a weekly basis using a validated visual analog scale (Flit et al, 2000)

Countries

Canada

Contacts

Primary ContactPeter Lemon, PhD
plemon@uwo.ca1 519 661 2111
Backup ContactSiobhan Smith, Bsc
ssmit422@uwo.ca

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026