NCT07414875

Brief Summary

Research on the benefits of apple cider vinegar has tended to focus on its hypoglycemic effects and lipid profile changes during long-term consumption, without exploring its acute effects on oxidative stress during short-term consumption. Therefore, this study aimed to determine whether apple cider vinegar consumption affects postprandial plasma MDA levels in obese adults. The hypothesis of this study is that apple cider vinegar consumption has an acute effect on changes in postprandial plasma MDA levels in obese adult subjects. Subject criteria are adults aged 19-59 years; obese nutritional status; based on a BMI of ≥ 25.0 kg/m² (according to the Asia-Pacific classification); in good general health. Exclusion criteria include pregnancy, breastfeeding, and menopause; consuming alcohol; intolerance to apple cider vinegar or fermented products. This preliminary study, a parallel, randomized, open-label, controlled clinical trial, compared two groups: a control group receiving a standard diet without apple cider vinegar, and an intervention group receiving a standard diet with a single dose of apple cider vinegar.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
46

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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 Start

First participant enrolled

February 4, 2026

Completed
7 days until next milestone

First Submitted

Initial submission to the registry

February 11, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

February 17, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 6, 2026

Completed
5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 11, 2026

Completed
Last Updated

June 9, 2026

Status Verified

June 1, 2026

Enrollment Period

3 months

First QC Date

February 11, 2026

Last Update Submit

June 6, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Change in Postprandial Plasma Malondialdehyde Levels

    Change in plasma malondialdehyde concentration from baseline (fasting) to the postprandial time point following acute administration of apple cider vinegar compared with control.

    Baseline (fasting) to 3 hours postprandial

Study Arms (2)

Apple Cider Vinegar Group

EXPERIMENTAL

Participants in this group received a single acute dose of apple cider vinegar administered before or with a standard test meal. Plasma malondialdehyde levels were measured before and after the meal.

Dietary Supplement: apple cider vinegar

Control Group

NO INTERVENTION

Participants in this group received a standard test meal without apple cider vinegar. Plasma malondialdehyde levels were measured before and after the meal.

Interventions

apple cider vinegarDIETARY_SUPPLEMENT

A single oral dose of apple cider vinegar was administered before a standard test meal to assess post-meal changes in plasma malondialdehyde levels.

Apple Cider Vinegar Group

Eligibility Criteria

Age19 Years - 59 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Adults aged 19-59 years.
  • Obese, based on a BMI of ≥ 25.0 kg/m² (according to the Asia-Pacific classification).
  • In good general health.
  • No diagnosed chronic diseases (e.g diabetes mellitus, heart disease, kidney disease, cancer, hepatitis, or chronic infections).
  • Willing to participate in the entire study and sign an informed consent form.

You may not qualify if:

  • Pregnant, breastfeeding, or menopausal women.
  • Alcohol consumption.
  • Intolerance to apple cider vinegar or fermented products.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ministry of Youth and Sports of the Republic of Indonesia (KEMENPORA RI)

Jakarta, Jakarta Special Capital Region, Indonesia

Location

MeSH Terms

Conditions

Obesity

Condition Hierarchy (Ancestors)

OverweightOvernutritionNutrition DisordersNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Ika Handayani, MD

    Faculty of Medicine, University of Indonesia

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Model Details: Participants are randomly assigned into two parallel groups: an apple cider vinegar intervention group and a control group. Each group receives a single acute intervention followed by postprandial assessment of plasma malondialdehyde levels.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

February 11, 2026

First Posted

February 17, 2026

Study Start

February 4, 2026

Primary Completion

May 6, 2026

Study Completion

May 11, 2026

Last Updated

June 9, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

Locations