Evidence map›Paper›PMID 41135814›Full record

ArticleContemporary clinical trials2025

Rationale and protocol for a randomized parallel intervention trial of two intermittent fasting approaches in patients with type 2 diabetes.

Felicia L Steger, Joseph E Donnelly, Robert N Montgomery, Lauren Clark, Corby K Martin, John M Miles, Kristine Grdinovac, Annie E Henderson, John P Thyfault

Abstract readClinical Trial Protocol
In one paragraph

Article in Contemporary clinical trials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Felicia L StegerDivision of Endocrinology, Diabetes, and Clinical Pharmacology and KU Diabetes Institute; Department of Internal Medicine, University of Kansas Medical Center, Kansas City, KS, USA; Department of Dietetics and Nutrition, University of Kansas Medical Center, Kansas City, KS, USA; Kansas Center for Metabolism and Obesity Research, Kansas City, KS, USA. Electronic address: fsteger@kumc.edu.
Joseph E DonnellyKansas Center for Metabolism and Obesity Research, Kansas City, KS, USA; Division of Physical Activity and Weight Management, Department of Internal Medicine, University of Kansas Medical Center, Kansas City, KS, USA.
Robert N MontgomeryDepartment of Biostatistics and Data Science, University of Kansas Medical Center, Kansas City, KS, USA.
Lauren ClarkDepartment of Biostatistics and Data Science, University of Kansas Medical Center, Kansas City, KS, USA.
Corby K MartinIngestive Behavior Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA, USA.
John M MilesDivision of Endocrinology, Diabetes, and Clinical Pharmacology and KU Diabetes Institute; Department of Internal Medicine, University of Kansas Medical Center, Kansas City, KS, USA; Kansas Center for Metabolism and Obesity Research, Kansas City, KS, USA.
Kristine GrdinovacDivision of Endocrinology, Diabetes, and Clinical Pharmacology and KU Diabetes Institute; Department of Internal Medicine, University of Kansas Medical Center, Kansas City, KS, USA.
Annie E HendersonDivision of Endocrinology, Diabetes, and Clinical Pharmacology and KU Diabetes Institute; Department of Internal Medicine, University of Kansas Medical Center, Kansas City, KS, USA.
John P ThyfaultDivision of Endocrinology, Diabetes, and Clinical Pharmacology and KU Diabetes Institute; Department of Internal Medicine, University of Kansas Medical Center, Kansas City, KS, USA; Kansas Center for Metabolism and Obesity Research, Kansas City, KS, USA; Department of Cell Biology and Physiology, The University of Kansas Medical Center, Kansas City, KS, USA.

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2012 to 2026
$69.1M
RADx-UP: Improving the Response of Local Urban and Rural Communities to Disparities in Covid-19 TestingUL1TR002366 · NCATS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Mario Castro, JAMES STEVEN LEEDER · 2017 to 2026
$44.3M
Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI ROBERT A KESTERSON · 2005 to 2026
$26.5M
longitudinal assessment of stress and stress-related concepts across a behavioral weight loss interventionP20GM144269 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI John P Thyfault, STEVEN A WEINMAN · 2022 to 2026
$14.9M
NCATS NIH HHS UL1 TR002366NIDDK NIH HHS L30 DK137346NIDDK NIH HHS P30 DK072476NIGMS NIH HHS P20 GM144269NIGMS NIH HHS U54 GM104940
6 · The paper itself

Abstract

backgroundType 2 diabetes (T2D) is a progressive disease driven by insulin resistance and β-cell dysfunction, often exacerbated by excess body weight. Intermittent fasting (IF) approaches, including intermittent energy restriction (IER) and time-restricted eating (TRE), have shown promise for improving glycemic control and facilitating diabetes remission. However, the feasibility and effectiveness of these IF approaches in individuals with T2D remain underexplored.

objectiveThis study aims to compare the feasibility, acceptability, and metabolic effects of IER and TRE in a randomized parallel trial in adults with T2D.

methodsAdults with T2D (N = 56) and overweight/obesity will be randomized to one of two interventions: IER (550-800 kcal/day on 2-3 days/week) or TRE (caloric intake within an 8-h daily window). Both groups will receive a comprehensive, remotely delivered diabetes education and behavioral support program over 6 months, followed by a 6-month low-contact follow-up during which participants continued the intervention on their own. Primary outcomes include feasibility (recruitment, retention, adherence) and acceptability. Secondary outcomes include changes in HbA1c, insulin sensitivity, insulin response to a mixed-meal tolerance test, body composition, and diabetes remission. Continuous glucose monitoring, metabolic and behavioral phenotyping will inform predictors of response.

conclusionThis study is the first parallel trial to compare IER and TRE in patients with T2D and overweight/obesity. Results will provide critical data on the metabolic and behavioral responses to each IF approach, informing future strategies to personalize nutrition therapy in T2D.

Indexed as

Caloric RestrictionDiabetes Mellitus, Type 2Intermittent FastingAdultBlood GlucoseFeasibility StudiesFemaleGlycated HemoglobinHumansInsulinInsulin ResistanceMaleMiddle AgedObesityOverweightRandomized Controlled Trials as TopicBlood GlucoseGlycated Hemoglobinhemoglobin A1c protein, humanInsulinGlycemic controlIntermittent fastingObesityType 2 diabetesWeight loss

Identifiers

PMID41135814
PMCPMC13186290

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.