Randomized controlled trial2025

Alternate-day fasting elicits larger changes in fat mass than time-restricted eating in adults without obesity - A randomized clinical trial

Derron N, Güntner AT, Weber IC, Braun J, Koska İÖ, Othman A, Mönch L, von Eckardstein A, Puhan MA, Beuschlein F, Hochuli M, Zamboni N, Guggenberger R, Gerber PA

Clinical nutrition (Edinburgh, Scotland) · 3 citations

Review labels

Funding not disclosed

Neutral facts our review recorded about how this study was done. They describe method, never whether we like the result.

How it was studied

Design
Randomized controlled trial (indexed by PubMed)
Studied in
People
Main outcome
Health markers and function

Who paid for it

Funding
Funding not disclosed

Publication

Published
2025-09-03 · Clin Nutr · vol. 53 · pp. 212–221
Publisher
Elsevier BV
Cited
4 citations · more than 88% of similar papers · 2.2× the field average
References
65 works
Access
Open access (hybrid journal) · CC-BY
Research areas
Dietary Effects on Health · Diet and metabolism studies · Enhanced Recovery After Surgery
Keywords
Medicine, Obesity, Fat mass, Randomized controlled trial, Intermittent fasting, Internal medicine, Clinical trial, Endocrinology
MeSH
adipose tissue, humans, weight loss, body mass index, fasting, body composition, energy metabolism, energy intake, time factors, quality of life, adolescent, adult, female, male, overweight, young adult

14 authors

From CH, DE

  • Nina DerronUniversity Hospital Zurich
  • Andreas Thomas GüntnerUniversity Hospital Zurich
  • Ines C. WeberUniversity of Zurich; University Hospital Zurich
  • Julia BraunUniversity of Zurich
  • İlker Ö KoskaUniversity Hospital Zurich
  • Alaa OthmanETH Zurich

Abstract

Background & aims

Intermittent fasting (IF) is a popular nutritional strategy for weight control and improved metabolic health, however it is unclear which type of intermittent fasting is most effective. This randomized trial directly compared short-term alternate-day fasting (ADF) and time-restricted eating (TRE) with controls in adults with overweight or a high normal weight. The aim was to compare the effects of ADF and TRE versus controls regarding whole-body fat mass loss, weight control and cardiometabolic health.

Methods

In this 4-week, parallel-arm, randomized clinical trial (February 2021-May 2022), participants aged 18-40 years with a body mass index between 23 and 30 kg/m2 were assigned to ADF (alternating fasting and ad libitum eating days), to TRE (eating only between 12:00-20:00), or control (no change in eating times). The primary outcome was change in total fat volume (assessed by whole-body magnetic resonance imaging). Secondary outcomes were subcutaneous and visceral fat mass, body weight, resting metabolic rate, biochemical markers, energy intake, activity energy expenditure and health-related quality of life.

Results

Seventy-six participants (mean [standard deviation (SD)] age, 29.6 [5.6] years; body mass index, 25.8 [2.2] kg/m2; 34 [44 %] female) were randomized to ADF (n = 26), TRE (n = 26), or control (n = 24). Seventy-five participants completed the trial (25 in ADF, 26 in TRE, 24 in control). ADF led to a greater reduction in total fat volume than control (mean difference -1059.8 cm3, 95 % CI: -1380.0 cm3 to -739.6 cm3, p 3, 95 % CI: -1013.9 to -377.6 cm3, p 3, 95 % CI: -621.3 cm3 to -106.7 cm3, p = 0.007). Energy intake was reduced by 34 % [18 %] in ADF, 15 % [21 %] in TRE and 3 % [22 %] in control. ADF, but not TRE, reduced visceral fat mass, resting metabolic rate, triiodothyronine and non-HDL cholesterol compared to controls. Only ADF increased activity energy expenditure and health-related quality of life. No serious adverse events occurred.

Conclusions

In this randomized clinical trial, ADF was more effective in reducing energy intake than TRE which has subsequent effects on fat mass and body weight. Only ADF improved several cardiometabolic risk factors.

Registration

https://clinicaltrials.gov/study/NCT04732130; Unique identifier: NCT04732130.

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

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