Food Replacement on Weight Control in Overweight Volunteers

June 28, 2024 updated by: Pornanong Aramwit, Pharm.D., Ph.D, Chulalongkorn University

Efficacy and Safety of Food Replacement on Weight Control in Overweight Volunteers

Volunteers will be divided into two groups which are protein and oil supplement group and normal dietary group. For protein and oil supplement group, they will take 1 sachet of product replaced dinner every day for 8 weeks. For normal dietary group, they will take regular dinner every day for 8 weeks. Weight, body mass index, body composition, waist and hip circumference, skin fold thickness, and chemistry in blood will be evaluated.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Not yet recruiting

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.

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 (Estimated)

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.
60

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

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Age 18-60 years
  • Body mass index more than 23 kg/m2
  • No heart disease, diabetes mellitus, thyroid disease, cancer, liver and kidney diseases
  • Wiling to attend the study

Exclusion Criteria:

  • Allergic to protein, grains, guar gum
  • Take medicine, supplement, herbal substance for weight control within 1 month
  • During intermittent fasting
  • Take birth control pill, steroids, anti-depressant drugs, and anti-epilepsy drugs
  • Cushing syndrome's
  • Pregnancy and lactation

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: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

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.
Experimental: Protein and oil supplement
Take 1 sachet/day replaced dinner
Dietary supplement: Protein and oil supplement
Take 1 sachet/day replaced dinner
No Intervention: Normal dietary meal
Take normal dietary meal for dinner

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
Weight
Time Frame: 8 weeks
Weight of volunteers (kg)
8 weeks

Secondary Outcome Measures

Secondary Outcome Measures

In a clinical study's protocol, a planned outcome measure that is not as important as the primary outcome measure for evaluating the effect of an intervention but is still of interest. Most clinical studies have more than one secondary outcome measure.
Outcome Measure
Measure Description
Time Frame
Body mass index
Time Frame: 8 weeks
Body mass index of volunteers (kg/m2)
8 weeks
Percentage of body fat
Time Frame: 8 weeks
Percentage of body fat (%) using bioelectrical impedance analysis (BIA)
8 weeks
Percentage of visceral fat
Time Frame: 8 weeks
Percentage of visceral fat (%) using bioelectrical impedance analysis (BIA)
8 weeks
Percentage of subcutaneous fat
Time Frame: 8 weeks
Percentage of subcutaneous fat (%) using bioelectrical impedance analysis (BIA)
8 weeks
Percentage of muscle
Time Frame: 8 weeks
Percentage of muscle (%) using bioelectrical impedance analysis (BIA)
8 weeks
Waist Circumference
Time Frame: 8 weeks
Waist Circumference (cm)
8 weeks
Hip Circumference
Time Frame: 8 weeks
Hip Circumference (cm)
8 weeks
Skin fold thickness
Time Frame: 8 weeks
Skin fold thickness (mm) using Skinfold Caliper
8 weeks
Total cholesterol
Time Frame: 8 weeks
Blood total cholesterol (mg/dL)
8 weeks
Low density lipoprotein
Time Frame: 8 weeks
Low density lipoprotein (mg/dL) in blood
8 weeks
High density lipoprotein
Time Frame: 8 weeks
High density lipoprotein (mg/dL) in blood
8 weeks
Triglycerides
Time Frame: 8 weeks
Triglycerides (mg/dL) in blood
8 weeks
Fasting blood sugar
Time Frame: 8 weeks
Fasting blood sugar (mg/dL) in blood
8 weeks
Hemoglobin A1C
Time Frame: 8 weeks
Hemoglobin A1C (%) in blood
8 weeks
Total protein
Time Frame: 8 weeks
Total protein (g/dL) in blood
8 weeks
Hemoglobin
Time Frame: 8 weeks
Hemoglobin (g/dL) in blood
8 weeks
SIRT1 (NAD-dependent deacetylase sirtuin-1)
Time Frame: 8 weeks
SIRT1 (NAD-dependent deacetylase sirtuin-1) (%) in blood
8 weeks
8-hydroxy-2-deoxyguanosine
Time Frame: 8 weeks
8-hydroxy-2-deoxyguanosine (%) in blood
8 weeks
Blood urea nitrogen
Time Frame: 8 weeks
Blood urea nitrogen (mg/dL) in blood
8 weeks
Creatinine
Time Frame: 8 weeks
Creatinine (mg/dL) in blood
8 weeks
Aspartate transaminase
Time Frame: 8 weeks
Aspartate transaminase (U/L) in blood
8 weeks
Alanine aminotransferase
Time Frame: 8 weeks
Alanine aminotransferase (U/L) in blood
8 weeks
Alkaline phosphatase
Time Frame: 8 weeks
Alkaline phosphatase (U/L) in blood
8 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.
Chulalongkorn University

Collaborators

Collaborators

An organization other than the sponsor that provides support for a clinical study. This support may include activities related to funding, design, implementation, data analysis, or reporting.
Mae Fah Luang 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 (Estimated)

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.
July 15, 2024

Primary Completion (Estimated)

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.
April 30, 2025

Study Completion (Estimated)

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.
May 15, 2025

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).
June 28, 2024

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.
June 28, 2024

First Posted (Actual)

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.
July 5, 2024

Study Record Updates

Last Update Posted (Actual)

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.
July 5, 2024

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.
June 28, 2024

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.
June 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

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.
  • EC23238-20

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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