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Effect of Intermittent Fasting on Fat Mass

Not Applicable
Conditions
Obesity
Interventions
Behavioral: Fasting
Registration Number
NCT04245007
Lead Sponsor
Indonesia University
Brief Summary

This study is aimed to assess the different effect on fat mass between fasting (intervention) group and not fasting (control) group after 8 weeks 5:2 intermittent fasting (IF) among obese male student aged 18-25. Female students are excluded because if they do any restriction intake during their menstruation period which is a lot of blood lost, it will be a risk for them.

This study is designed as non-blinding randomized control trial. Subject who adhere with less than 85 percent fasting (14 out of 16) will be dropped out from this study. Total sample in this study is 62 students which are 31 students for each group.

Detailed Description

5:2 intermittent fasting (IF) is eating pattern in which no or few calories are consumed for 13 hours (for 5 am to 6 pm) done in two non-consecutive days days per week, followed by ad libitum intake on the remaining days, without any requirement of water restriction.

Subjects will be distributed to each group by using randomization block of four.

This study will use 8 forms consist of; informed consent, subject selection form, re-anthropometric measurement form, questionnaire, semi quantitative food frequency questionnaire (SQ-FFQ), international physical activity questionnaire (IPAQ), food record book, and control and evaluation form. While the tolls are consist of food photograph book (to help in filling the food record book), body height scale, and bio-electrical impedance analysis (BIA) Seca medical body composition analyzer (mBCA) 515/514 (to measure body composition).

Recruitment & Eligibility

Status
UNKNOWN
Sex
Male
Target Recruitment
62
Inclusion Criteria
  • obese male student age 18-25
  • do not have experience on amputation
  • willingness to participate in the whole study by signing informed consent
Exclusion Criteria
  • hypertrophy muscle students identified from body composition measurement
  • in a certain diet at the moment
  • consuming lipid-lowering drug at the moment
  • doing regular fasting (2 days a week) for 2 months before the study begin
  • suffer from chronic illness (confirmed by disease history form
  • using electronic implants, for example pacemaker or pane
  • using prostheses (artificial body part)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InterventionFastingSubject will ask to do 5:2 intermittent fasting (2 non-consecutive days a week) within 8 weeks
Primary Outcome Measures
NameTimeMethod
Fat mass8 weeks

reduction fat mass in the intervention group measured by bio-electrical impedance analysis

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Indonesia University

🇮🇩

Depok, West Java, Indonesia

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