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Effect of HINEX Jelly on Nutritional Status in People With Possible Sarcopenia or Sarcopenia

Primary Purpose

Sarcopenia

Status
Active
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
HINEX Jelly ( jelly high protein supplement)
Sponsored by
Taipei Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sarcopenia

Eligibility Criteria

40 Years - 85 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: 40-85 years old, middle-aged and elderly subjects with possible sarcopenia or sarcopenia. According to AWGS 2019, possible sarcopenia is defined as (1) handgrip strength < 28 kg in men and < 18 kg in women or (2) 5-time chair stand test ≥ 12 seconds; sarcopenia is defined as meet (1) or (2) plus appendicular skeletal muscle mass index (ASMI) < 7.0 kg/m2 in men and < 5.7 kg/m2 in women. Exclusion Criteria: BMI>35 kg/m2, Taking any special diet (i.e. vegan), be allergic to ingredient (i.e. milk or soy bean) and any seriously acute or chronic lung, liver, kidney, gastrointestinal, cancers diseases history.

Sites / Locations

  • Taipei Medical University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

first intervention group (Supp-Con sequence)

post intervention group (Con-Supp sequence)

Arm Description

The first intervention group used HINEX Jelly as daily breakfast during the first to 8th weeks of the experiment, the 9th to 12th week is the wash out period, the 13th to the 20th week is the selfcontrol period.

the post-intervention group is in the first to the 8th week of self-control period,the 9th to 12th week is the wash out period, and the 13th to the 20th week is used HINEX Jelly as daily breakfast.

Outcomes

Primary Outcome Measures

muscle mass
the change of muscle mass and measured via bioelectrical impedance analysis(BIA)
hand grip strength
the change of hand grip strength as the marker of muscle strength.Measured via hand grip dynamometry.
5-time chair stand test
the change of 5-time chair stand test as the marker of physical performance.

Secondary Outcome Measures

short physical performance battery
the change of short physical performance battery as the marker of physical performance.
6-meter gait speed
the change of 6-meter gait speed as the marker of physical performance.
Mini nutritional assessment
the change of 6-meter gait speed as the marker of nutritional status.

Full Information

First Posted
June 19, 2023
Last Updated
June 28, 2023
Sponsor
Taipei Medical University
Collaborators
Taiwan Otsuka Pharm. Co., Ltd
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1. Study Identification

Unique Protocol Identification Number
NCT05926375
Brief Title
Effect of HINEX Jelly on Nutritional Status in People With Possible Sarcopenia or Sarcopenia
Official Title
Effect of HINEX Jelly on Nutritional Status in People With Possible Sarcopenia or Sarcopenia
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 5, 2022 (Actual)
Primary Completion Date
March 24, 2023 (Actual)
Study Completion Date
June 28, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Taipei Medical University
Collaborators
Taiwan Otsuka Pharm. Co., Ltd

4. Oversight

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

5. Study Description

Brief Summary
HINEX Jelly is a jelly high protein supplement. This report is to investigate whether jelly high protein supplement can achieve greater muscle mass, muscle strength, physical performance and nutritional status in sarcopenia or possible sarcopenia subjects. It is 20 weeks randomized, crossover, self-controlled trials. The screening, recruitment and trial period were carried out from Feb, 2022 to Mar, 2023. Patients were randomized to either a self-controlled phase,which intake 400~500 kcal breakfast, or a supplement phase consume one servings of jelly high protein supplement (303 kcal, 15 g protein and 2400 mg BCAA per serving) and 100~200 kcal food at breakfast per day, for 8 weeks. After a 4-week washout they cross over to the alternate treatment. The anthropometric measurements, sarcopenia parameters, nutritional assessment and hematology assessment data were measured at the week 0,8,12,20 and 24-hour dietary record were recorded at week 1,8,13,20.
Detailed Description
Parameters of sarcopenia, including the muscle mass assessment, handgrip strength and physical performance assessment.Muscle mass and body composition were measured by bioelectrical impedance analysis (BIA). A hand dynamometer was used to measure handgrip strength. Physical performance was measured by short physical performance battery (SPPB), 6-meter gait speed and 5-time chair stand test. Mini nutritional assessment (MNA) used to measure nutritional status. The hematology assessment including total protein, albumin, pre-albumin, transferrin, c-reactive protein (CRP), vitamin D, calcium, glucose, insulin, homeostasis model assessment-estimated insulin resistance (HOMA-IR), total cholesterol, triacylglycerol, creatinine, creatine-kinase, alkaline phosphatase, glutamic oxaloacetic transaminase (GOT), glutamic pyruvic transaminase (GPT) and complete blood count.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
The experiment lasted for 20 weeks, including 8 weeks self-controlled phase, 8 weeks supplement phase and 4 weeks washout period. In self-controlled phase would intake 400~500 kcal breakfast and in supplement phase consume one servings of jelly high protein supplement with 100~200 kcal food at breakfast. Subjects were randomly divided into "first intervention group" and "post intervention group". The first intervention group used HINEX Jelly as daily breakfast during the first to 8th weeks of the experiment, the 9th to 12th week is the wash out period, the 13th to the 20th week is the selfcontrol period; the post-intervention group is in the first to the 8th week of self-control period,the 9th to 12th week is the wash out period, and the 13th to the 20th week is used HINEX Jelly as daily breakfast, as well as maintained their regular diet and medication, but do exercise lifestyle modification during 20-week experimental period.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
first intervention group (Supp-Con sequence)
Arm Type
Experimental
Arm Description
The first intervention group used HINEX Jelly as daily breakfast during the first to 8th weeks of the experiment, the 9th to 12th week is the wash out period, the 13th to the 20th week is the selfcontrol period.
Arm Title
post intervention group (Con-Supp sequence)
Arm Type
Experimental
Arm Description
the post-intervention group is in the first to the 8th week of self-control period,the 9th to 12th week is the wash out period, and the 13th to the 20th week is used HINEX Jelly as daily breakfast.
Intervention Type
Dietary Supplement
Intervention Name(s)
HINEX Jelly ( jelly high protein supplement)
Intervention Description
In self-controlled phase,which intake 400~500 kcal breakfast, or in supplement phase consume one servings of jelly high protein supplement (303 kcal, 15 g protein and 2400 mg BCAA per serving) and 100~200 kcal food at breakfast per day, for 8 weeks.
Primary Outcome Measure Information:
Title
muscle mass
Description
the change of muscle mass and measured via bioelectrical impedance analysis(BIA)
Time Frame
week 0,8,12,20
Title
hand grip strength
Description
the change of hand grip strength as the marker of muscle strength.Measured via hand grip dynamometry.
Time Frame
week 0,8,12,20
Title
5-time chair stand test
Description
the change of 5-time chair stand test as the marker of physical performance.
Time Frame
week 0,8,12,20
Secondary Outcome Measure Information:
Title
short physical performance battery
Description
the change of short physical performance battery as the marker of physical performance.
Time Frame
week 0,8,12,20
Title
6-meter gait speed
Description
the change of 6-meter gait speed as the marker of physical performance.
Time Frame
week 0,8,12,20
Title
Mini nutritional assessment
Description
the change of 6-meter gait speed as the marker of nutritional status.
Time Frame
week 0,8,12,20
Other Pre-specified Outcome Measures:
Title
General clinical chemistry of blood lipid
Description
the change of lipid profile (total cholesterol and triglyceride) and measured via automated clinical chemistry analyzer
Time Frame
week 0,8,12,20
Title
General clinical chemistry of blood sugar
Description
the change of blood sugar (glucose, insulin) and measured via automated clinical chemistry analyzer. Use the glucose, insulin concentration to calculate homeostasis model assessment-estimated insulin resistance (HOMA-IR).
Time Frame
week 0,8,12,20
Title
General clinical chemistry of liver function
Description
the change of liver function function ( glutamic oxaloacetic transaminase (GOT), glutamic pyruvic transaminase (GPT)) and measured via automated clinical chemistry analyzer
Time Frame
week 0,8,12,20
Title
General clinical chemistry of kidney function
Description
the change of liver function and kidney function (creatinine) and measured via automated clinical chemistry analyzer
Time Frame
week 0,8,12,20
Title
General clinical chemistry of nutritional status
Description
the change of nutritional status (total protein in g/dL, albumin in g/dL, pre-albumin in mg/dL, transferrin in mg/dL) and measured via automated clinical chemistry analyzer
Time Frame
week 0,8,12,20
Title
General clinical chemistry of vitamin D status
Description
the change of vitamin D status and measured via automated clinical chemistry analyzer
Time Frame
week 0,8,12,20
Title
C-reactive protein (CRP)
Description
the change of inflammatory marker C-reactive protein (CRP) measured via automated clinical chemistry analyzer
Time Frame
week 0,8,12,20
Title
Tumor Necrosis Factor-α(TNF-α)
Description
the change of inflammatory marker Tumor Necrosis Factor-α(TNF-α) measured via commercial kit
Time Frame
week 0,8,12,20

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 40-85 years old, middle-aged and elderly subjects with possible sarcopenia or sarcopenia. According to AWGS 2019, possible sarcopenia is defined as (1) handgrip strength < 28 kg in men and < 18 kg in women or (2) 5-time chair stand test ≥ 12 seconds; sarcopenia is defined as meet (1) or (2) plus appendicular skeletal muscle mass index (ASMI) < 7.0 kg/m2 in men and < 5.7 kg/m2 in women. Exclusion Criteria: BMI>35 kg/m2, Taking any special diet (i.e. vegan), be allergic to ingredient (i.e. milk or soy bean) and any seriously acute or chronic lung, liver, kidney, gastrointestinal, cancers diseases history.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jane C-J Chao, Ph.D.
Organizational Affiliation
Taipei Medical University, Taiwan, R.O.C.
Official's Role
Study Chair
Facility Information:
Facility Name
Taipei Medical University
City
New Taipei City
State/Province
Zhonghe Dist.
ZIP/Postal Code
235
Country
Taiwan

12. IPD Sharing Statement

Plan to Share IPD
No

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Effect of HINEX Jelly on Nutritional Status in People With Possible Sarcopenia or Sarcopenia

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