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Monitoring During Different Intermittent Fasting Protocols in Non-Obese Adults

NCT04732130 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 76

Last updated 2023-10-06

No results posted yet for this study

Summary

LIMITFOOD is a randomized clinical intervention study that investigates the effects of two different intermittent fasting protocols compared to a control group on the health of normal- and overweight adults. A total of 72 participants will be randomized into three equally sized groups: an alternate day fasting, a time-restricted feeding and a control group.

Conditions

  • Intermittent Fasting
  • Overweight
  • Time Restricted Feeding

Interventions

BEHAVIORAL

Time-Restricted Feeding

Participants are instructed to limit food intake to maximum 8 hours per day.

BEHAVIORAL

Alternate Day Fasting

Participants are instructed to fast every other day.

Sponsors & Collaborators

  • Philipp Gerber

    lead OTHER

Principal Investigators

  • Philipp Gerber, MD · University of Zurich

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-03-10
Primary Completion
2023-07-01
Completion
2023-07-01

Countries

  • Switzerland

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04732130 on ClinicalTrials.gov