Actively Recruiting

Phase Not Applicable
Age: 60Years +
All Genders
ID05525039

Dissecting the Therapeutic Mechanism of a Combined Vibration Treatment and HMB Supplement to Combat Sarcopenia

Led by Chinese University of Hong Kong · Updated on 2025-02-13

200

Participants Needed

3

Research Sites

N/A

Total Duration

On this page

Sponsors

C

Chinese University of Hong Kong

Lead Sponsor

A

Abbott

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the combined effect of vibration treatment (VT) and -hydroxy -methylbutyrate (HMB) supplementation on sarcopenia, a condition characterized by muscle loss and weakness in older adults. A previous animal study showed that this combination reduced fat infiltration, increased lean muscle mass, and improved muscle strength. This study aims to confirm these benefits in people aged 60 and above who show signs of sarcopenia, with the goal to slow its progression by improving muscle mass, strength, and performance. Participants will be randomly assigned to one of four groups: control (protein supplement only), HMB supplement only, VT only, or both HMB and VT together. VT involves using a device delivering low-magnitude, high-frequency vibrations (0.3g, 35Hz) for 20 minutes per day at least three times a week, while HMB is taken as a daily 3g oral supplement. All groups receive daily protein supplements for six months. Outcomes will be measured at the start, midpoint, and end of the six-month treatment period. During the study, participants will undergo assessments including handgrip strength, gait speed, muscle mass by DXA, balance tests, and quality of life surveys. These evaluations will occur at baseline, 3 months, and 6 months to monitor changes. The primary focus is on muscle strength and physical performance. The study is single-blinded and conducted by the Chinese University of Hong Kong, with careful monitoring throughout the six-month duration.

CONDITIONS

Brief Title

RCT of Combination Effect of Vibration Treatment and HMB Supplementation on Myosteatosis and NMJ Degeneration

Who Can Participate

Age: 60Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Subjects aged 60 years or above
  • Subjects who have sarcopenia based on AWGS algorithm including low skeletal muscle mass by bioelectrical impedance, low handgrip strength, and/or slow gait speed
Not Eligible

You will not qualify if you...

  • Subjects with pathological bone diseases
  • Subjects with chronic inflammatory conditions such as rheumatoid arthritis
  • Subjects with neurological problems affecting gait
  • Subjects receiving regular supervised exercise more than 3 times per week
  • Subjects who are chair-bound or bed-bound
  • Subjects with malignancy
  • Subjects with cardiovascular concerns such as having a pacemaker
  • Subjects with acute fractures or severe osteoarthritis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Participants are screened by SARC-F, handgrip, gait speed, and bioelectric impedance assessments based on the AWGS definition.

Treatment

Duration - 6 months

Participants receive assigned interventions including vibration treatment, HMB supplement, and daily protein supplement according to their group assignment.

Visits at baseline, 3 months, and 6 months post-treatment at the investigators' institute for outcome assessments.

Trial Site Locations

Total: 3 locations

1

Evangelical Luthera Church Social Service - Hong Kong

Hong Kong, Hong Kong

Active, Not Recruiting

2

The Chinese University of Hong Kong Jockey Club Centre for Osteoporosis Care and Control

Hong Kong, Hong Kong

Actively Recruiting

3

The Chinese University of Hong Kong, Department of Orthopaedics and Traumatology, 1/F Li Ka Shing Outpatient Clinic (North), PWH

Hong Kong, Hong Kong

Actively Recruiting

Loading map...

Research Team

W

Wing Hoi Cheung, PhD

M

Meng Chen Michelle Li, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

4

Similar Trials

A Multicenter, Randomized, Double-Blind, Placebo-controlled ...

Sarcopenia in Elderly

Actively Recruiting

4 locations

Study of Silkworm Pupa Powder to Improve Nutritional Status ...

AD - Alzheimer's Disease

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

Published Research Related To This Trial

Effects of 18-month low-magnitude high-frequency vibration on fall rate and fracture risks in 710 community elderly--a cluster-randomized controlled trial.

K S Leung, C Y Li, Y K Tse...

https://pubmed.ncbi.nlm.nih.gov/24676848

Vibration and β-hydroxy-β-methylbutyrate treatment suppresses intramuscular fat infiltration and adipogenic differentiation in sarcopenic mice.

Jinyu Wang, Can Cui, Yu Ning Chim...

https://pubmed.ncbi.nlm.nih.gov/31994349

Effect of β-hydroxy-β-methylbutyrate (HMB) on lean body mass during 10 days of bed rest in older adults.

Nicolaas E P Deutz, Suzette L Pereira, Nicholas P Hays...

https://pubmed.ncbi.nlm.nih.gov/23514626

Effects of exercise and nutrition supplementation in community-dwelling older Chinese people with sarcopenia: a randomized controlled trial.

Liu-Ying Zhu, Ruth Chan, Timothy Kwok...

https://pubmed.ncbi.nlm.nih.gov/30462162

Biophysical and nutritional combination treatment for myosteatosis in patients with sarcopenia: a study protocol for single-blinded randomised controlled trial.

Meng Chen Michelle Li, Yu Kin Cheng, Can Cui...

https://pubmed.ncbi.nlm.nih.gov/38176874