CClinicalTrials.gg
Status unknownNCT05309057Updated Apr 4, 2022

Network Meta-analysis of Intermittent Fasting and Cardiometabolic Risk

An observational study in Obesity, PreDiabetes and Diabetes, sponsored by University of Toronto. Status unknown at 2 sites in Canada. Per ClinicalTrials.gov, last updated 2022-04-04.

Sponsored by University of Toronto · Observational

The sponsor has not verified this record recently (last verified Mar 2022), so the status shown — last known as Active, not recruiting — may be out of date.
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
25
Sex
All
01

Study summary

Intermittent fasting is a method of restricting calories over a defined period of time and includes regimens such as whole-day fasting, alternate-day fasting, and time-restricted feeding. There is emerging evidence that intermittent fasting or energy restriction might be more beneficial than continuous energy restriction for some risk factors. The effect of intermittent fasting on risk factors associated with obesity, diabetes, and cardiovascular disease, however, is not clear. The European Association for the Study of Diabetes (EASD) has yet to make any recommendations regarding the role of intermittent fasting in the management of diabetes. To inform the update of the EASD Clinical Practice Guidelines for Nutrition Therapy, tthe Diabetes and Nutrition Study Group (DNSG) of the EASD has commissioned a systematic review and network meta-analysis of randomized controlled trials of the effect of different intermittent fasting strategies on established cardiometabolic risk factors. The findings generated by this proposed knowledge synthesis will shape guide current guidelines and improve health outcomes by educating healthcare providers and patients, and by guiding future research design.

Read the detailed description

Background: 'Intermittent fasting' is currently the most popular trending diet, yet its clinical utility remains unclear. Previous systematic reviews and meta-analyses of intermittent fasting have been limited by a narrow focus on weight loss, one specific method of intermittent fasting, and/or a subset of participants who would be the least likely to benefit. Other issues have included unexplained heterogeneity, incorrect analyses and/or lack of assessment of the certainty of the evidence. There is emerging evidence that intermittent fasting may improve cardiometabolic risk markers independent of calories. However, there is a lack of certainty about the effectiveness of intermittent fasting on overall cardiometabolic risk across different health conditions, and the differences between the various methods of intermittent fasting. The European Association for the Study of Diabetes (EASD) has yet to make any recommendations regarding the role of intermittent fasting in the management of diabetes. To inform the update of the EASD Clinical Practice Guidelines for Nutrition Therapy, the Diabetes and Nutrition Study Group (DNSG) of the EASD has commissioned a systematic review and network meta-analysis (an approach which has the advantage over traditional pairwise meta-analyses of being able to assess simultaneously multiple interventions) to assess the effect of the different strategies of intermittent energy restriction (intermittent fasting) versus continuous energy restriction and ad libitum diets on cardiometabolic risk in randomized controlled trials and assess the certainty of evidence using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach.

Objective: To assess simultaneously the effect of the various strategies of intermittent energy restriction (intermittent fasting), continuous energy restriction, and ad libitum diets on body weight and other cardiometabolic risk factors in a systematic review and network meta-analysis of randomized trials using the GRADE approach.

Design: Each systematic review and meta-analysis will be conducted according to the Cochrane Handbook for Systematic Reviews of Interventions and reported according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for network meta-analyses (PRISMA-Network).

Data sources: MEDLINE, EMBASE, and The Cochrane Central Register of Controlled Trials (Clinical Trials; CENTRAL) will be searched using appropriate search terms. These searches will be supplemented by hand searches of references of included studies. Abstracts will be included and no language restrictions will be used.

Study selection: The investigators will include randomized controlled trials (RCTs) that are >=3-weeks duration investigating the effect of intermittent fasting, continuous caloric restriction and/or ad libitum diets on cardiometabolic risk factors in adults.

Data extraction: Two or more investigators will independently extract relevant data. Standard computations and imputations will be used to derive missing variance data. All disagreements will be resolved by consensus.

Risk of bias: Risk of bias will be assessed using the Cochrane Risk of Bias (RoB) Tool by the two or more investigators.

Outcomes: There will be 10 outcome clusters. The primary outcome will be body weight. Secondary outcomes will be other markers of adiposity (BMI, body fat, waist circumference); glycemic control (glycated blood proteins [HbA1c, fasting blood glucose, postprandial blood glucose, fasting blood insulin, homeostasis model assessment of insulin resistance [HOMA-IR]); established therapeutic lipid targets (LDL-cholesterol, non-HDL-cholesterol, apolipoprotein B [apo B], HDL-cholesterol, triglycerides); blood pressure (systolic blood pressure and diastolic blood pressure); markers of NAFLD (intrahepatocellular lipids [IHCL], alanine aminotransferase [ALT], aspartate aminotransferase [AST]); uric acid; and markers of inflammation (CRP).

Data synthesis: The investigators will perform a network meta-analysis comparing all the interventions simultaneously. These interventions will include alternate day fasting, cyclical whole day fasting, time restricted feeding, continuous energy restriction, and ad libitum diet in a single analysis by combining both direct and indirect evidence across the selected network of studies. Separate pooled analyses will be conducted for each cardiometabolic risk factor using the random-effects network meta-analysis. Intrasitivity will be adjudged using incoherence. Global method of incoherence (design-by-treatment interaction) and inconsistency factors (disagreement between direct and indirect estimates) will be used to estimate incoherence. A-priori subgroup analyses (health status, age, control diet energy restriction, diet supervision, study design, follow-up, feeding control, randomization, energy balance, baseline body weight, funding source, and ROB) will be performed. Separate analysis will be performed in people with diabetes. Publication bias will be assessed if there are ≥10 comparisons. The overall certainty of the evidence for each outcome will be assessed with GRADE using the CINeMA approach.

Evidence Assessment: The certainty of the evidence for each outcome will be assessed using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach.

Knowledge translation plan: The results will be disseminated through interactive presentations at local, national, and international scientific meetings and publication in high impact factor journals. Target audiences will include the public health and scientific communities with interest in nutrition, diabetes, obesity and cardiovascular disease. Feedback will be incorporated and used to improve the public health message and key areas for future research will be defined. Applicant/Co-applicant decision makers will network among opinion leaders to increase awareness and participate directly as committee members in the development of future guidelines.

Significance: The proposed project will be the most comprehensive synthesis and evaluation of the totality of evidence on the role of intermittent fasting in cardiometabolic health. These findings will aid in strengthening current guidelines and improve health outcomes by informing shared clinical decision making between healthcare providers and patients and guiding future research.

02

Conditions studied

  • Obesity
  • PreDiabetes
  • Diabetes
  • Hypertension
  • NAFLD
  • Metabolic Syndrome
  • Dyslipidemias
  • Inflammation
  • Gout
  • Cardiometabolic Syndrome
  • Cardiovascular Diseases

Keywords

  • Intermittent fasting
  • Continuous energy restriction
  • Weight loss
  • Systematic review and meta-analysis
  • Network metanalysis
  • Randomized controlled trial
  • Clinical practice guideline
  • Adiposity
  • Glycemic control
  • Blood pressure
  • Blood lipids
  • NAFLD markers
  • Uric acid
  • inflammatory markers
  • Cardiometabolic risk factors
03

In context

Cardiovascular Diseases

4,904 studies on the registry are indexed under Cardiovascular Diseases; 920 are open to participants now.

This study's planned enrollment of 25 is below the median of 573 across 1,483 observational studies indexed under Cardiovascular Diseases.

Browse Cardiovascular Diseases studies →

Lead sponsor

University of Toronto is the lead sponsor of 397 studies on the registry; 59 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Adults of all health statuses.

Inclusion criteria

  • Randomized controlled trials in humans
  • Intermittent fasting intervention
  • Continuous energy restriction, ad libitum diet, or other intermittent fasting diet as comparators
  • Diet duration ≥1 weeks
  • Data for at least one prespecified outcome
  • Viable outcome data

Exclusion criteria

Exclusion Criteria:

  • Non-human studies
  • Observational studies
  • Children
  • Multi-modal interventions
  • Diet duration \< 1 weeks
  • No viable outcome data
  • Lack of suitable comparator
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
25 participants (estimated)
Patient registry
No

Groups and cohorts

  • Studies with intermittent fasting

    Studies with intermittent fasting strategies.

    Dietary Supplement: Intermittent Fasting

Interventions

  • Dietary supplementIntermittent Fasting

    Methods of intermittent fasting strategies, continuous energy restriction, and ad libitum diet.

06

What researchers measure

Primary outcomes

  1. Body weight

    Body weight in kg

    Time frame: Through study completion, up to 20 years

Secondary outcomes

  1. Adiposity - BMI

    Body mass index (BMI) in kg/m2

    Time frame: Through study completion, up to 20 years

  2. Adiposity - Waist circumference

    Waist circumference in cm

    Time frame: Through study completion, up to 20 years

  3. Adiposity - Body fat

    Body fat in % (relative units)

    Time frame: Through study completion, up to 20 years

  4. Glycemic control - HbA1c

    Glycemic control - HbA1c

    Time frame: Through study completion, up to 20 years

  5. Glycemic control - fasting plasma glucose (FPG)

    Fasting plasma glucose (FPG) in mmol/L

    Time frame: Through study completion, up to 20 years

  6. Glycemic control - 2h plasma glucose (2h-PG)

    2h plasma glucose (2h-PG) during a 75g oral glucose tolerance test (OGTT) in mmol/L

    Time frame: Through study completion, up to 20 years

  7. Glycemic control - fasting plasma insulin (FPI)

    Fasting plasma insulin (FPI) in pmol/L

    Time frame: Through study completion, up to 20 years

  8. Glycemic control - homeostasis model assessment of insulin resistance (HOMA-IR)

    Homeostasis model assessment of insulin resistance (HOMA-IR)

    Time frame: Through study completion, up to 20 years

  9. Established blood lipid targets - LDL-cholesterol (LDL-C)

    LDL-cholesterol (LDL-C) in mmol/L

    Time frame: Through study completion, up to 20 years

  10. Established blood lipid targets - non-HDL-cholesterol (non-HDL-C)

    non-HDL-cholesterol (non-HDL-C) in mmol/L

    Time frame: Through study completion, up to 20 years

  11. Established blood lipid targets - apolipoprotein B (apo B)

    Apolipoprotein B (apo B) in g/L

    Time frame: Through study completion, up to 20 years

  12. Established blood lipid targets - triglycerides

    Triglycerides in mmol/L

    Time frame: Through study completion, up to 20 years

  13. Established blood lipid targets - HDL-cholesterol (HDL-C)

    HDL-cholesterol (HDL-C) in mmol/L

    Time frame: Through study completion, up to 20 years

  14. Blood pressure - Systolic blood pressure (SBP)

    Systolic blood pressure (SBP) in mmHg

    Time frame: Through study completion

  15. Blood pressure - diastolic blood pressure (DBP)

    Diastolic blood pressure (DBP) in mmHg

    Time frame: Through study completion, up to 20 years

  16. Markers of non-alcoholic fatty liver disease (NAFLD) - Intrahepatocellular lipids (IHCL)

    Intrahepatocellular lipids (IHCL) in % (relative units)

    Time frame: Through study completion, up to 20 years

  17. Markers of non-alcoholic fatty liver disease (NAFLD) - alanine transaminase (ALT)

    Alanine transaminase (ALT) in U/L

    Time frame: Through study completion, up to 20 years

  18. Uric acid

    Uric acid in mmol/L

    Time frame: Through study completion, up to 20 years

  19. Markers of inflammation - CRP

    CRP in mg/dL

    Time frame: Through study completion, up to 20 years

07

Study locations

2 sites
  • Clinical Nutrition and Risk Factor Modification Centre, St. Michael's Hospital
    Toronto, Ontario M5C 2T2, Canada
  • Faculty of Medicine
    Toronto, Ontario, Canada
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 4, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05309057
Lead sponsor
University of Toronto
Responsible party
John Sievenpiper (Professor, University of Toronto) — Principal investigator
First posted
Apr 4, 2022
Start date
Nov 1, 2020
Primary completion
Jun 2022 (estimated)
Completion
Aug 2022 (estimated)
Last update
Apr 4, 2022

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Mar 2022. You cannot join it, but the record below documents what was studied.

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