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Intermittent Fasting on Body Fat and Quality of Life

The Effect of Intermittent Fasting on Body Fat and Quality of Life

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06307275
Enrollment
70
Registered
2024-03-12
Start date
2024-03-11
Completion date
2026-12-01
Last updated
2026-05-06

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

Conditions

Healthy

Brief summary

The purpose of this investigator-initiated study to check the feasibility that intermittent fasting has on body fat loss and quality of life.

Detailed description

Start of study: Informed Consent, Body Fat Analysis, Questionnaires on quality of life, sleep, and stress. For the next four weeks, participants will eat their normal food intake with no restrictions on when to eat. Participants will keep their normal weekly exercise routine. Midway of study: Body Fat Analysis, Questionnaires on quality of life, sleep, and stress. For the next four weeks, participants will do the intermittent fasting program. This program has participants fasting 16 hours from their last meal of the previous evening's meal to the first meal of their next day. Then for 8 hours, participants are able to eat. During the fasting, participants are allowed to consume water and black coffee/tea. Participants will also keep their normal weekly exercise routine. End of study: Body Fat Analysis, Questionnaires on quality of life, sleep, and stress.

Interventions

OTHERFasting

Fasting for 16 hours from participant last meal of the previous evening's meal to the first meal of the next day. Then for 8 hours, participant is able to eat. During the fasting, participants are allowed to consume water and black coffee/tea. Participants will also keep their normal weekly exercise routine.

Participants will not be fasting during these four weeks. They will eat their normal food intake and keep their normal physical activity levels.

Sponsors

Loma Linda University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

• In good health

Exclusion criteria

• Diabetes or Metabolic Syndrome

Design outcomes

Primary

MeasureTime frameDescription
Body fat percentagechange between baseline and eight weeksBody composition will give the following measurement: body fat percentage
Visceral fatchange between baseline and eight weeksIn addition, body composition will also give us visceral fat measurement

Countries

United States

Contacts

CONTACTGurinder Bains, PhD
gbains@llu.edu909-558-4000
PRINCIPAL_INVESTIGATORGurinder Bains, PhD

Loma Linda University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 7, 2026