Protein Supplementation Intervention for Improving Muscle Mass and Physical Performance in Older People With Sarcopenia

Sarcopenia Clinical Trial

Official title:

Protein Supplementation Intervention for Improving Muscle Mass and Physical Performance in Older People With Sarcopenia: A Randomized, Double-blind, Placebo-controlled Trial

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04516421
• Other study ID #: JWang20-CF01
• Status: Active, not recruiting
• Phase: N/A
• Start date: August 24, 2020
• Est. completion date: June 30, 2022

Study information

• Verified date: February 2022
• Source: Asia University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Background: Declines in muscle mass and strength are expected with aging, but physical inactivity and low protein intake have been suggested as risk factors of sarcopenia. So far, lifestyle interventions, especially exercise and nutritional supplementation, prevail as mainstays of treatment for sarcopenia.

Objective: To explore the effect and benefits of protein supplementation on the improvement of muscle mass and physical performance in older people with sarcopenia.

Design: A randomized, double-blind, placebo-controlled clinical trial. Methods: Participants aged 65-95y who meet the following criteria will be invited: (1) muscle mass: bioimpedance, <7.0 kg/m² (male) and <5.7 kg/m² (female), (2) handgrip strength: <28 kg (male) and <18 kg (female), and (3) low physical performance: 6-m gait Speed <1.0 m/s. Study participants will be randomly assigned to two groups. The experimental group will receive a 12-week intervention with【protein (14g)+ BCAA(4.4g)】 drink per day, while the parallel control group will receive a placebo oat drink per day.

Participants in the control group will be asked to maintain participants' usual diet and physical activity. There are 3 time-points to measure outcomes and observe other required information, at week 0(baseline), 6 and 12.

Description:

Background: Sarcopenia is defined as an abnormal loss of muscle mass and strength. Declines in muscle mass and strength are expected with aging, but physical inactivity and low protein intake have been suggested as risk factors of sarcopenia. Recently, Taiwan is known as the fastest-aging nation in the world, and the prevalence of sarcopenia has been reported as 3.9-7.3%; even more 9-64% in Dr. Chen's study. So far, lifestyle interventions, especially exercise and nutritional supplementation, prevail as mainstays of treatment for sarcopenia.

Objective: To explore the effect and benefits of protein supplementation on the improvement of muscle mass and physical performance in older people with sarcopenia.

Study design: A randomized, double-blind, placebo-controlled clinical trial which will be conducted between September and November, 2020.

Participants: The study will be conducted in Keelung, Taiwan. A total of 9 day-care centers, including 180 over 65 years of residents, will be invited to participate the study via telephone calls.

Eligible participants will be invited to attend this randomized, double-blind, placebo-controlled, 2-parallel-groups trial, and will be randomly assigned to the experimental and control groups with 1:1 ratio.

Intervention: The intervention period will be 12 weeks. The control group will receive 150c.c placebo oat drink (1.5g protein, 0.5g fat, 0.1g carbohydrate each pack, Zhan Xuan Co. Ltd., Taiwan) per day, five days per week, while the experimental group will receive 150c.c protein supplementation drink (14g protein, 0.6g fat, 7g carbohydrate, 4.4 g BCAA , 2.4g glutamate, 0.5g arginine and 0.4g taurine each pack, Affix Health, Taiwan Branch) per day, five days per week.

Supplementation in the experimental group contains 90 kcal/d and the placebo oat drink contains 8.3kcal/d. Participants in the control group will be asked to maintain participants' usual diet and physical activity. There are 3 time-points to measure outcomes and observe other required information, at week 0(baseline), 6 and 12.

Sample size calculation: Referring to the setting in a published paper that gave a sample size of 30 participants/group, a sample size of 40 participants in each group is considered in the study, by considering potential dropouts.

Random assignment and blinding: An independent external researcher prepared a computer generated cluster random sampling. After random assignment, the external researcher newly assigned a subject ID to each participant. All other study personnel and participants remained blinded to the identity codes throughout the course of the study. When participants withdrew from or completed the study, researchers were provided with the participants' identities, and the participants were told what supplement participants had received.

Ethical approval: The study was approved by Taipei Hospital Human Trial Committee of the Ministry of Health and Welfare. All participants were assured that data collected from participants would be strictly confidential, and the physical condition and safety were given priority. Investigators conducted intervention only after obtaining participants ethical approval (registration number: TH-IRB-00190046). Anyone who feel uncomfortable during the study will be allowed to quit immediately with no any restriction.

Study measurement: Kihon Checklist, MNA, GDS-SF, SPPB, IADL, MMSE, handgrip, 6m gait speed, (SMI), SF-12 questionnaire and Tw-FROP-Com.

Statistical methods: Statistical analysis was conducted using the IBM SPSS software (version 22, IBM Corporation, New York, NY). An intention-to-treat analysis was performed. (1) Descriptive statistics: describe the distribution of category variables by number and percentage, and the mean and standard deviations describe the distribution of continuous variables. (2) Inference statistics: chi-square: to verify whether the pre-measured category variants between the experimental group and the control group are homogeneous. ANOVA: Check whether the continuous variables measured between the experimental group and the control group are homogeneous. Generalized estimating equations (GEE) with interactions of time and group in the models will be conducted to evaluate the intervention effect. A two-sided p-value < 0.05 is considered statistically significant.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 80
• Est. completion date: June 30, 2022
• Est. primary completion date: June 30, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 65 Years to 95 Years

Eligibility

Inclusion Criteria:

• 65-95 years old

• can communicate in Mandarin or Taiwanese language

• sacorpenia (basing on criteria of Asian Working Group for Sarcopenia )

Exclusion Criteria:

• with liver or kidney disease

• stent in body.

Related Conditions & MeSH terms

• Sarcopenia

Intervention

Dietary Supplement:
• Protein supplementation
The experimental group contained 14g protein, 0.6g fat, 7g carbohydrate, 4.4 g BCAA , 2.4g glutamate, 0.5g arginine and 0.4g taurine with 90 kcal/pack (Affix Health, Taiwan Branch).
• Placebo oat drink
placebo oat drink contained 1.5g protein, 0.5g fat, 0.1g carbohydrate with 8.3kcal/pack (Zhan Xuan, Co. Ltd., Taiwan).

Locations

Country	Name	City	State
Taiwan	Keelung First Daycare Center	Keelung
Taiwan	Keelung Hospital Daycare Center, Ministry of Health and Welfare	Keelung
Taiwan	Keelung Second Daycare Center	Keelung

Sponsors (1)

Lead Sponsor	Collaborator
Asia University

Country where clinical trial is conducted

Taiwan, 

References & Publications (1)

Chen LK, Woo J, Assantachai P, Auyeung TW, Chou MY, Iijima K, Jang HC, Kang L, Kim M, Kim S, Kojima T, Kuzuya M, Lee JSW, Lee SY, Lee WJ, Lee Y, Liang CK, Lim JY, Lim WS, Peng LN, Sugimoto K, Tanaka T, Won CW, Yamada M, Zhang T, Akishita M, Arai H. Asian — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Short Physical Performance Battery ("change" is being assessed)	The SPPB includes usual walking speed 4 m, five chair-stands test, and balance test. A score (scale: 0-4) is assigned to performance on time to rise five times from a seated position, standing balance, and 4-m walking velocity. participants receive a score of 0 for unable to complete each task. Summing the three individual categorical scores, a summary performance score is created for each participant (range: 0-12), with higher scores indicating better body function. In the walking test, the participants could use a cane, a walker, or other walking aid but the aid of another person. The cut-off value is ?9 according to the AWGS 2019.	The change is assessed from week 0 (baseline) to week 12
Other	Instrumental Activities of Daily Living ("change" is being assessed)	There are eight domains of function measured with the Lawton IADL scale. Women are scored on all 8 areas of function; historically, for men, the areas of food preparation, housekeeping, laundering are excluded. A summary score ranges from 0 (low function, dependent) to 8 (high function, independent) for women, and 0 through 5 for men. There are 3 of 5 ( Shopping,Mode of Transportation, Food Preparation,Laundry and Housekeeping) in need of assistance is mild inability.	The change is assessed from week 0 (baseline) to week 12
Other	Mini-Mental State Examination ("change" is being assessed)	The MMSE scores may be used to classify the severity of cognitive impairment or to document serial change in dementia participants. A full score of 30 indicates that the higher score means better cognitive function. The following four cut-off levels should be employed to classify the severity of cognitive impairment: no cognitive impairment 24-30; mild cognitive impairment 19-23; moderate cognitive impairment 10-18; and severe cognitive impairment =9.	The change is assessed from week 0 (baseline) to week 12
Other	Falls Risk for Older People Community setting-Taiwan Version ("change" is being assessed)	The tool consists of 13 factors being rated, most on a graded 0-3 scale, and thus ranges from 0 to 60. A higher score indicates a higher risk. The fall risk score can be divided into 3 levels: high(19- 60), medium(12- 18) and light( 0 - 11).	The change is assessed from week 0 (baseline) to week 12
Other	Medical Outcome Study Short Form-12 ("change" is being assessed)	The SF-12 which provides information on mental and physical health status is a shortened version of the SF-36. The SF-12 uses the same eight domains as the SF-36. The total score is from 0 to 8. The higher the score, the better quality of life.	The change is assessed from week 0 (baseline) to week 12
Other	Geriatric depression scale-short form ("change" is being assessed)	GDS-SF is a measure designed to explore depression associated with the elderly. There are a total of 15 self-made scales of questions, each of which respondents only have to answer yes or no.The total score is 15 , the cutoff values is 5, more than 5 means depression symptoms, the higher score , the higher degree of depression.	The change is assessed from week 0 (baseline) to week 12
Other	Kihon Checklist-Chinese ("change" is being assessed)	A tool for measuring the degree of frailty of the elderly, There were 25 test assessments in the scale, and if there were more than five, the weaker the participantes were.	The change is assessed from week 0 (baseline) to week 12
Other	Taiwan-Mini Nutritional Assessment ("change" is being assessed)	It is a nutritional assessment scale suitable for Taiwan's elderly over 65years old with severe malnutrition. The total score is 14. The higher score means more better. The score of 12-14 means normality, 8-11 means malnutrition-risk, and less and equal 7 means malnutrition.	The change is assessed from week 0 (baseline) to week 12
Primary	Skeletal muscle mass index ("change" is being assessed)	Bioimpedance is adopted to assess sarcopenia. Therefore, Skeletal muscle mass index is measured by bioimpedance( using the In body instrument Model 230) and means ASM/H²((sum of lean muscle mass in upper and lower limb divided by square of body height). Skeletal muscle mass index is used with a cut-off value of 7 kg/m² in men, and 5.4 kg/m² in women according to the AWGS 2020.	The change is assessed from week 0 (baseline) to week 12
Secondary	Hand-grip strength ("change" is being assessed)	The maximal hand grip strength is measured using a Camry (Model:EH101) hand dynamometer. The investigator will demonstrate how to use the dynamometer, then participants will be asked to press for 3 to 5 seconds on the grip using the greatest possible force. The measurement is repeated after a 30-second rest. Both hands will be measured separately and the highest score is registered. The cut-off value of hand-grip is <28 kg for men and <18 kg for women according to the AWGS 2019..	The change is assessed from week 0 (baseline) to week 12
Secondary	Gait speed ("change" is being assessed)	Gait speed means measurement of 6 meters walking speed. The cut-off value of gait speed is <1.0 m/s according to the AWGS 2019.	The change is assessed from week 0 (baseline) to week 12