Cohort study2018Open access

Intermittent Fasting (Alternate Day Fasting) in Healthy, Non-obese Adults: Protocol for a Cohort Trial with an Embedded Randomized Controlled Pilot Trial

Tripolt NJ, Stekovic S, Aberer F, Url J, Pferschy PN, Schröder S, Verheyen N, Schmidt A, Kolesnik E, Narath SH, Riedl R, Obermayer-Pietsch B, Pieber TR, Madeo F, Sourij H

Advances in therapy · 20 citations

How it was studied

Design
Cohort study (indexed by PubMed)
Studied in
People
Main outcome
Health markers and function

Who paid for it

Funding
Independent funding
Government
Austrian Science Fund
University or hospital
BioTechMed-Graz
Government
Austrian Science Fund FWF
Grants
Austrian Science Fund (P 27893); Austrian Science Fund (P29203); Austrian Science Fund (P 29262)

Based on 3 listed funder(s) and full-text disclosure statement.

Publication

Published
2018-07-25 · Adv Ther · vol. 35 · issue 8 · pp. 1265–1283
Publisher
Adis, Springer Healthcare
Cited
23 citations · more than 86% of similar papers · 1.9× the field average
References
63 works
Access
Open access (hybrid journal) · CC-BY-NC
Research areas
Dietary Effects on Health · Diet and metabolism studies · Genetics, Aging, and Longevity in Model Organisms
Keywords
Medicine, Randomized controlled trial, Intermittent fasting, Cohort, Calorie, Weight loss, Internal medicine, Blood pressure, Physical therapy, Obesity
MeSH
humans, hypertension, obesity, blood glucose, clinical protocols, caloric restriction, fasting, cohort studies, prospective studies, pilot projects, energy intake, adult, female, male, randomized controlled trials as topic

15 authors

From AT

  • Norbert Joachim TripoltMedical University of Graz
  • Slaven StekovicUniversity of Graz
  • Felix AbererMedical University of Graz
  • Jasmin UrlMedical University of Graz; Center For Biomarker Research In Medicine
  • Peter N. PferschyMedical University of Graz; Center For Biomarker Research In Medicine
  • Sabrina S. SchröderUniversity of Graz

Abstract

Background/objectives

Alternate day fasting (ADF) is a subtype of intermittent fasting and is defined as a continuous sequence of a fast day (100% energy restriction, zero calories) and a feed day (ad libitum food consumption), resulting in roughly 36-h fasting periods. Previous studies demonstrated weight reductions and improvements of cardiovascular risk factors with ADF in obese subjects. However, rigorous data on potential endocrine, metabolic and cardiovascular effects, besides weight loss, are lacking. Therefore we aim to investigate the short- and mid- to long-term clinical and molecular effects of ADF in healthy non-obese subjects.

Methods

We will perform a prospective cohort study with an embedded randomized controlled trial (RCT) including 90 healthy subjects. Thirty of them will have performed ADF for at least 6 months (mid-term group). Sixty healthy subjects without a particular diet before enrolment will serve as the control group. These subjects will be 1:1 randomized to either continuing their current diet or performing ADF for 4 weeks. All subjects will undergo study procedures that will be repeated in RCT participants after 4 weeks. These procedures will include assessment of outcome parameters, dual-energy X-ray absorptiometry, measurement of endothelial function, an oral glucose tolerance test, 24-h blood pressure measurement, retinal vessel analysis, echocardiography and physical activity measurement by an accelerometer. Blood, sputum, buccal mucosa and faeces will be collected for laboratory analyses. Participants in the RCT will wear a continuous glucose monitor to verify adherence to the study intervention.

Planned outcomes

The aim of this project is to investigate the effects of ADF on human physiology and molecular cellular processes. This investigation should gain in-depth mechanistic insights into the concept of ADF and form the basis for larger subsequent cohort recruitment and consecutive intervention studies.

Trial registration

NCT02673515; registered 24 November 2015. Current protocol date/version: 7 February 2017/version 1.8.

Abstract via Europe PMC. Copyright remains with the authors or publisher (CC BY-NC).

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