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CompletedNCT05136313Updated Oct 1, 2024

Healthy vs Unhealthy Obesity: Mehanistic Insights and Effects of Time-Restricted Eating

An interventional study of Time-restricted eating in Metabolically Healthy Obesity and Intermittent Fasting, sponsored by Instituto de Nutrición y Tecnología de los Alimentos. Completed at 1 site in Chile. Open to male participants aged 18 Years to 25 Years. Per ClinicalTrials.gov, last updated 2024-10-01.

Sponsored by Instituto de Nutrición y Tecnología de los Alimentos · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
53
Allocation
Non-randomized
Ages
18 Years to 25 Years
Sex
Male
01

Study summary

Obesity-related cardiometabolic diseases are now a leading cause of death worldwide. These diseases result from a dysfunctional adipose tissue (AT) that induces inflammation, insulin resistance and altered endocrine function. However, not all obese people develop metabolic complications, which has given rise to the concept of "metabolically healthy obesity" (MHO). Recent evidence suggests that intermittent fasting methods, in particular time-restricted eating (TRE) may be effective in improving cardiometabolic health, independently of weight loss, and this could be particularly effective in MUO subjects. The investigators hypothesize that in young male adults TRE is a more effective/beneficial approach in MUO than in MHO due to the weight loss-independent improvement in their inflammatory and metabolic derangements. To this aim, a 16-week 8h TRE intervention study will be performed in MHO and MUO subjects, assessing anthropometric, endocrine, and other outcomes.

Read the detailed description

Although clinical differences between metabolically healthy and unhealthy obesity (MHO and MUO, respectively) have been extensively described, cellular mechanisms involved in these different phenotypes are largely unknown. This evidence is crucial for proposing preventive and therapeutic approaches. Recently, intermittent fasting methods, in particular time-restricted eating (TRE, a self-selected daily limited eating window protocol), have shown to be effective in improving cardiometabolic health, independently of weight loss, which could be particularly relevant in MUO.

The investigators will recruit young (20-22y-old) males with obesity (Body Mass Index≥30) and classify them as MHO or MUO (≤1 or ≥3 metabolic syndrome risk factors, respectively). A 16-week, 8h TRE intervention will be conducted in MHO vs. MUO subgroups, to assess and compare the anthropometric, metabolic, endocrine, inflammatory and peripheral blood mononuclear cell (PBMC) mechanistic/signaling response.

The investigators expect to advance the understanding of cellular mechanisms implicated in MHO and MUO, including potential therapeutic targets. Ultimately, the investigators expect to find relevant opportunities for intervention to prevent the serious cardiometabolic consequences of obesity.

02

Conditions studied

  • Metabolically Healthy Obesity
  • Intermittent Fasting

Keywords

  • Time restricted eating
  • Metabolic health
  • PBMC
  • Adipokines
03

In context

Obesity

6,296 studies on the registry are indexed under Obesity; 1,692 are open to participants now.

This study's enrollment of 53 is below the median of 78 across 4,878 interventional studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

Instituto de Nutrición y Tecnología de los Alimentos is the lead sponsor of 3 studies on the registry; none are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 25 Years
Sexes eligible
Male
Accepts healthy volunteers
No

Inclusion criteria

  • Belong to the GOCS cohort at INTA
  • BMI≥30
  • Own and use a Smartphone with Apple iOS or Android OS
  • Baseline eating period ≥ 13 h per day.

Exclusion criteria

Exclusion Criteria:

  • Medications for any metabolic syndrome disorder
  • Shift workers
  • Known inflammatory and/or rheumatologic disease
  • History of cardiovascular event
  • Thyroid or adrenal disease, malignancy or diabetes
  • History of eating disorder.
  • Special diet (e.g., celiac disease),or any other disease or treatment that may interfere with the study.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
53 participants (actual)

Study arms

  • Experimental
    MHO

    metabolically healthy obese subjects undergoing TRE

    Behavioral: Time-restricted eating

  • Experimental
    MUO

    metabolically unhealthy obese subjects undergoing TRE

    Behavioral: Time-restricted eating

Interventions

  • BehavioralTime-restricted eating

    16 weeks of TRE consisting of an 8-hour eating window.

    Also known as: Time-restricted feeding, Intermittent fasting

06

What researchers measure

Primary outcomes

  1. TG

    Fasting triglycerides

    Time frame: 16 weeks

Secondary outcomes

  1. Waist circumference

    Time frame: 16 weeks

07

Study locations

1 site
  • INTA, Universidad de Chile
    Santiago, RM 7810000, Chile
08

References and documents

Individual participant data

Plan to share: Undecided

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 Oct 1, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05136313
Lead sponsor
Instituto de Nutrición y Tecnología de los Alimentos
Collaborators
Agencia Nacional de Investigación y Desarrollo, Universidad Católica del Maule
Responsible party
Mariana Cifuentes (Professor, Instituto de Nutrición y Tecnología de los Alimentos) — Principal investigator
First posted
Nov 29, 2021
Start date
Jun 24, 2022
Primary completion
Jan 4, 2024
Completion
Jan 4, 2024
Last update
Oct 1, 2024

Study contacts

Mariana Cifuentes, PhD
principal investigator · Universidad de Chile INTA

Oversight

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

Not currently enrolling

This study is completed, as verified in Sep 2024. You cannot join it, but the record below documents what was studied.

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