Body Fat Percentage Prediction Model After Basic Combat Training on Army Candidate in Indonesia

November 10, 2023 updated by: Dwi Monik Purnamasari, Indonesia University

Body Fat Percentage Prediction Model of the Basic Combat Training Effect on Army Candidate' Body Composition in Indonesia

This research is a quantitative study using the Pre-Experimental Model One-Group Pretest-Posttest Design with total sampling from the Republic of Indonesia Defense University batch 4 cadets that fullfiled criteria. The intervention is 12 weeks basic combat training (only one group), a compulsory program for cadets.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Completed

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Detailed Description

the purpose of this study is know the effect of basic combat training on the anthropometry and body fat percentage prediction model of army cadets after basic combat training in Indonesia

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment (Actual)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
258

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Indonesia
    • West Java
      • Bogor, West Java, Indonesia, 16810
        • Indonesia Defense University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Students as fourth batch in bachelor program in Indonesia Defense University
  • Aged 16-18 years

Exclusion Criteria:

  • Drop out or resign from Indonesia Defense University during research
  • Having emergency condition during examination

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Screening
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm

Participant Group / Arm

A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment, or no intervention, according to the trial's protocol.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
Other: basic combat training
Pre experimental design, only one group with intervention basic combat training
Other: basic combat training (investigator did not design the intervention)
12 weeks basic combat training is 12 weeks is a compulsory program for all cadets accepted in republic indonesia defense university

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Measure Description
Time Frame
Anthropometry after basic combat training in cadets of Indonesia
Time Frame: 12 weeks
Pre post data of z score BMI for age based on who anhtroplus in standar deviation. Weight measured by BIA omron HBF 375, height measured by Microtoise OneMed. Height only measured once before combat training
12 weeks
Anthropometry after basic combat training in cadets of Indonesia
Time Frame: 12 weeks
Pre post data of weight in measured by BIA omron HBF 375
12 weeks
Anthropometry after basic combat training in cadets of Indonesia
Time Frame: 12 weeks
Pre post data of waist circumference in cm measured by non-elastic measuring tape OneMed OD 235.
12 weeks
Anthropometry after basic combat training in cadets of Indonesia
Time Frame: 12 weeks
Pre post data of triceps skinfold, bicep skinfold, subscapular skinfold, suprailiac skinfold, and skinfold thickness (aggregate measurement of tricep, bicep, subscapular, and suprailiac skinfold) in mm measured by Harpenden Caliper
12 weeks
Body composition after basic combat training in cadets of Indonesia
Time Frame: 12 weeks
Pre post data of body fat percentage in %, Whole body subcutaneous fat in %, whole body skeletal muscle in %, measured by BIA Omron type HBF 375
12 weeks
Body Fat Percentage Prediction Model of the Basic Combat Training (BCT) Effect on Army Candidate'
Time Frame: 12 weeks
Total and delta predictive equation formula of body fat percentage after BCT based on variables delta and total value before bct of z score bmi for age, waist circumference, skinfold thickness, sleep quality measured by psqi, total daily carbohydrate, calorie, protein, fat intake based on semi quantitave food frequency questionnaires for macronutrient in bahasa Indonesia, and physical activity measured by IPAQ questionairres in bahasa indonesia. Variables body fat percentage before bct include as predictor in total body fat percentage prediction equation formula after BCT
12 weeks
Sleep quality after basic combat training in cadets of Indonesia
Time Frame: 12 weeks
Pre post data in sleep quality using Pittsburgh Sleep Quality Index (psqi) questionnairres consist of 7 component sleep quality. The total score range from 0-21 points
12 weeks
Macronutrient intake before and after basic combat training in cadets of Indonesia
Time Frame: 12 weeks
Pre post data in total daily intake of carbohydrate,fat, and protein in grams and calories in kilo calorie based on semi quantitave food frequency questionnaires for macronutrient in bahasa Indonesia
12 weeks
Physical activity before and after basic combat training in cadets of Indonesia
Time Frame: 12 weeks
Pre post data of physical activity in Mets measured by The International Physical Activity Questionnaire (IPAQ) questionairres in bahasa indonesia
12 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Indonesia University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
May 17, 2023

Primary Completion (Actual)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
September 1, 2023

Study Completion (Actual)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
September 1, 2023

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
November 4, 2023

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
November 10, 2023

First Posted (Estimated)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
November 16, 2023

Study Record Updates

Last Update Posted (Estimated)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
November 16, 2023

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
November 10, 2023

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
November 1, 2023

More Information

Terms related to this study

Keywords

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • Ket- 105/UN2.F10.D11/PPM.00.02

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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