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Efficacy of Protein Supplemented Very Low Calorie Meals on Weight Loss

Primary Purpose

Obesity, Sarcopenic Obesity

Status
Unknown status
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Protein supplemented very low calorie diet program
Conventional low calorie diet program
Sponsored by
Seoul National University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Body Mass Index (BMI ) more than 25 kg/m2 or
  • Waist circumference more than 90 cm in men or 85 cm in women

Exclusion Criteria:

  • History of treatment with anti-obesity drugs or participation in another weight loss program in previous 6 months
  • Weight changes more than 3 kg during the 6 months before participation
  • Unstable cardiovascular events during the 6 months before participation
  • Uncontrolled mood disorder
  • History of eating disorder
  • History of alcohol use disorder
  • History of gallstone
  • Chronic renal failure (estimated glomerular filtration less than 30 ml/min)

Sites / Locations

  • Seoul National University Bundang Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Protein supplemented very low calorie diet program

Conventional low calorie diet program

Arm Description

The lifestyle intervention using protein supplemented very low calorie meals will be implemented with individual counseling sessions for 12 months. Initial intensive weight loss stage will be delivered during the first 4 month period with total meal replacement to partial meal replacement using protein supplemented very low calorie meals. During the weight loss maintenance stage, regular intermittent very low calorie meal replacement one week per month will be delivered for the entire period. Mobile counseling will be offered to help patients achieve weight loss as well as weight loss maintenance.

The conventional low calorie diet program will be offered to participants assigned to control group using educational material and individual counseling sessions for 12 months. Mobile counseling will be also offered for weight loss and weight loss maintenance.

Outcomes

Primary Outcome Measures

Changes in weight
Changes of weight loss from the baseline expressed as kg

Secondary Outcome Measures

Changes in body composition
Changes in muscle mass and fat mass from the baseline expressed as kg using bioelectrial impedance analysis (Inbody Co., Seoul, Korea)
Changes in systolic and diastolic blood pressure
Changes in systolic and diastolic blood pressure from the baseline expressed as mmHg
Changes in triglyceride
Changes in triglyceride from the baseline expressed as mg/dL
Changes in glucose
Changes in glucose from the baseline expressed as mg/dL
Changes in high density lipoprotein (HDL) Cholesterol
Changes in HDL cholesterol from the baseline expressed as mg/dL
Changes in low density lipoprotein (LDL) Cholesterol
Changes in LDL cholesterol from the baseline expressed as mg/dL
Changes in liver enzyme
Changes in aspartate and alanine aminotransferase, gamma glutamyltransferase (AST and ALT, GGT) from the baseline expressed as IU/L
Changes in insulin resistance
Changes in insulin resistance using the homeostatic model assessment for insulin resistance (HOMA-IR) as HOMA-IR =insulin(uIU/ml) * fasting glucose (mg/dL)*0.05551/22.5
Changes in obesity related quality of life
Changes in Korean version of obesity related quality of life scales (published in Korean Society for the Study of Obesity 2003;12(4):280-293 )

Full Information

First Posted
September 3, 2020
Last Updated
October 15, 2020
Sponsor
Seoul National University Hospital
Collaborators
Seoul National University Bundang Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04597788
Brief Title
Efficacy of Protein Supplemented Very Low Calorie Meals on Weight Loss
Official Title
The Role of Protein Supplemented Very Low Calorie Medical Meals on Weight and Metabolic Changes Among People With Obesity: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Unknown status
Study Start Date
November 16, 2020 (Anticipated)
Primary Completion Date
December 1, 2022 (Anticipated)
Study Completion Date
January 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Seoul National University Hospital
Collaborators
Seoul National University Bundang Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This randomized clinical trial will evaluate the efficacy and safety of protein supplemented very low calorie meals on weight loss and weight loss maintenance among people with obesity.
Detailed Description
Approximately 30% of the Korean population has obesity or abdominal obesity and is often accompanied by obesity related complications such as cardiovascular disease, diabetes, osteoarthritis and even some types of cancer. However, there are not many lifestyle modification treatments available that have long-term effects other than drugs and surgical treatments in the management of obesity. Preserving muscle mass should also be considered in weight loss especially for elderly adults with obesity, because decreased muscle mass and strength can negatively affect morbidity and mortality in the elderly. Therefore, the investigators want to evaluate the effectiveness and safety of the protein supplemented very low calorie meals on weight loss, body composition as well as metabolic changes compared with traditional low calorie low fat diet in people with obesity.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Sarcopenic Obesity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
104 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Protein supplemented very low calorie diet program
Arm Type
Experimental
Arm Description
The lifestyle intervention using protein supplemented very low calorie meals will be implemented with individual counseling sessions for 12 months. Initial intensive weight loss stage will be delivered during the first 4 month period with total meal replacement to partial meal replacement using protein supplemented very low calorie meals. During the weight loss maintenance stage, regular intermittent very low calorie meal replacement one week per month will be delivered for the entire period. Mobile counseling will be offered to help patients achieve weight loss as well as weight loss maintenance.
Arm Title
Conventional low calorie diet program
Arm Type
Active Comparator
Arm Description
The conventional low calorie diet program will be offered to participants assigned to control group using educational material and individual counseling sessions for 12 months. Mobile counseling will be also offered for weight loss and weight loss maintenance.
Intervention Type
Other
Intervention Name(s)
Protein supplemented very low calorie diet program
Intervention Description
Protein supplemented very low calorie meal is a shake-type meal replacement with total calories of 600 to 800 calories per day and proteins provided at 1.2g of ideal body weight per day. The four-month, very low calorie diet program schedule will be as follows. In the first two weeks, all three meals are replaced, followed by two meals replaced and one meal in food in the next six weeks, and one meal replacement is recommended for the next eight weeks. For the next eight months, the intermittent very low calorie meal replacements will be provided regularly for one week a month. If a subject gains weight more than 2kg, he or she will have an additional 1 week of two meal replacements, and if a subject gains weight more than 4kg, he or she should have an additional 2 weeks of replacement. Individual sessions will be held 11 times during the study. Mobile counseling with dietitians or nurses will be offered to help subjects lose weight and maintain weight loss.
Intervention Type
Other
Intervention Name(s)
Conventional low calorie diet program
Intervention Description
Low calorie diet consists of 1200 to 1500 calories will be educated and lifestyle modification will be encouraged for participants in control group. Educational materials as well as recipes for low calorie diet will be provided in individual sessions. Mobile counseling will also be offered for sticking to the diet program.
Primary Outcome Measure Information:
Title
Changes in weight
Description
Changes of weight loss from the baseline expressed as kg
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Changes in body composition
Description
Changes in muscle mass and fat mass from the baseline expressed as kg using bioelectrial impedance analysis (Inbody Co., Seoul, Korea)
Time Frame
12 months
Title
Changes in systolic and diastolic blood pressure
Description
Changes in systolic and diastolic blood pressure from the baseline expressed as mmHg
Time Frame
12 months
Title
Changes in triglyceride
Description
Changes in triglyceride from the baseline expressed as mg/dL
Time Frame
12 months
Title
Changes in glucose
Description
Changes in glucose from the baseline expressed as mg/dL
Time Frame
12 months
Title
Changes in high density lipoprotein (HDL) Cholesterol
Description
Changes in HDL cholesterol from the baseline expressed as mg/dL
Time Frame
12 months
Title
Changes in low density lipoprotein (LDL) Cholesterol
Description
Changes in LDL cholesterol from the baseline expressed as mg/dL
Time Frame
12 months
Title
Changes in liver enzyme
Description
Changes in aspartate and alanine aminotransferase, gamma glutamyltransferase (AST and ALT, GGT) from the baseline expressed as IU/L
Time Frame
12 months
Title
Changes in insulin resistance
Description
Changes in insulin resistance using the homeostatic model assessment for insulin resistance (HOMA-IR) as HOMA-IR =insulin(uIU/ml) * fasting glucose (mg/dL)*0.05551/22.5
Time Frame
12 months
Title
Changes in obesity related quality of life
Description
Changes in Korean version of obesity related quality of life scales (published in Korean Society for the Study of Obesity 2003;12(4):280-293 )
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Body Mass Index (BMI ) more than 25 kg/m2 or Waist circumference more than 90 cm in men or 85 cm in women Exclusion Criteria: History of treatment with anti-obesity drugs or participation in another weight loss program in previous 6 months Weight changes more than 3 kg during the 6 months before participation Unstable cardiovascular events during the 6 months before participation Uncontrolled mood disorder History of eating disorder History of alcohol use disorder History of gallstone Chronic renal failure (estimated glomerular filtration less than 30 ml/min)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ju Young Kim, MD, PhD
Phone
(82)1036964218
Email
kkamduri@snubh.org
Facility Information:
Facility Name
Seoul National University Bundang Hospital
City
Seongnam-si
State/Province
Gyeonggi-do
ZIP/Postal Code
463-707
Country
Korea, Republic of

12. IPD Sharing Statement

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Efficacy of Protein Supplemented Very Low Calorie Meals on Weight Loss

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