NCT07408791

Brief Summary

Prediabetes is a metabolic condition associated with increased risk of type 2 diabetes and cardiovascular disease. Intermittent fasting (IF) has emerged as a potential dietary intervention to improve metabolic health, yet comparative evidence among different IF patterns remains limited. This randomized controlled trial aims to evaluate the effects of three intermittent fasting regimens-5:2 fasting, alternate-day fasting, and time-restricted feeding-compared with a control diet on metabolic parameters, inflammatory markers, body composition, and nutrigenomic profiles in adults with prediabetes.

Trial Health

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Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
1mo left

Started Feb 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress74%
Feb 2026Jun 2026

Study Start

First participant enrolled

February 1, 2026

Completed
5 days until next milestone

First Submitted

Initial submission to the registry

February 6, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 13, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 31, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2026

Last Updated

February 13, 2026

Status Verified

February 1, 2026

Enrollment Period

4 months

First QC Date

February 6, 2026

Last Update Submit

February 6, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Metabolic Profile

    Change in Fasting Plasma Glucose (mg/dL)

    Baseline, Week 3, and Week 6

Secondary Outcomes (4)

  • Lipid Profile

    Baseline and Week 6

  • Nutrigenomics

    Baseline

  • Body Composition

    Baseline, Week 3, and Week 6

  • Inflammation Profile

    Baseline and Week 6

Study Arms (3)

Intermittent Fasting (16:8)

EXPERIMENTAL
Behavioral: Diet

5:2 Diet

ACTIVE COMPARATOR
Behavioral: Diet

Non Fasting

NO INTERVENTION

Interventions

DietBEHAVIORAL

Intermittent Fasting

5:2 DietIntermittent Fasting (16:8)

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Patients with prediabetes, defined according to ADA criteria (fasting plasma glucose 100-125 mg/dL or 2-hour postprandial glucose 140-199 mg/dL).
  • Willing to follow the fasting/diet intervention protocol for 4-6 weeks (depending on the study duration).
  • Signing informed consent and willing to be randomized into one of 3 intervention groups (Monday-Thursday Fasting/5:2, Alternate-Day Fasting/ADF, or Time-Restricted Fasting/IF).

You may not qualify if:

  • Diagnosis of type 2 diabetes mellitus.
  • Currently undergoing antidiabetic drug therapy (e.g., metformin, sulfonylurea, insulin).
  • Has a severe chronic disease (kidney failure, liver failure, heart failure, or eating disorder).
  • Pregnancy or breastfeeding.
  • History of eating disorders (anorexia nervosa, bulimia nervosa, or binge eating disorder).
  • Taking medications that affect glucose metabolism (e.g., systemic steroids, atypical antipsychotics, etc.). Diagnosis of type 2 diabetes

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Internal Medicine - Endocrinology Division, Faculty of Medicine, Universitas Sumatera Utara / RSUP H. Adam Malik Medan

Medan, North Sumatera, Indonesia

Location

MeSH Terms

Conditions

Glucose Intolerance

Interventions

Diet

Condition Hierarchy (Ancestors)

HyperglycemiaGlucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic Diseases

Intervention Hierarchy (Ancestors)

Nutritional Physiological PhenomenaDiet, Food, and NutritionPhysiological Phenomena

Central Study Contacts

Muhammad Aron Pase, MD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Prof

Study Record Dates

First Submitted

February 6, 2026

First Posted

February 13, 2026

Study Start

February 1, 2026

Primary Completion (Estimated)

May 31, 2026

Study Completion (Estimated)

June 30, 2026

Last Updated

February 13, 2026

Record last verified: 2026-02

Locations