Dissecting the Therapeutic Mechanism of an Effective Combination Treatment Targeting Neuromuscular Junction Dengeneration and Myosteatosis to Combat Sarcopenia

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Device, Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The investigators' pre-clinical study confirms the positive effects of combined treatment (VT + HMB) on reducing fat-to-lean tissue ratio, intramuscular fat infiltration and increasing muscle strength in sarcopenia animal model. The results showed that fat mass could be decreased by \ 32%, while histology Oil Red O staining indicated a decrease of fat by almost 60%; in contrast, lean muscle mass increased by \ 14%. On muscle strength, combined treatment increased twitch force, tetanic force and grip strength by \ 30-66%. These in vivo results are very encouraging and the investigators should explore its potential in clinical translation. As VT and HMB supplement have been commercially available and their compliance rates are satisfactory, they can be translated to clinical application easily. The investigators' next step is to confirm its clinical efficacy, so that sarcopenia becomes a new indication of VT and HMB. The hypothesis is that combined treatment of VT and HMB can retard the progression of sarcopenia in human, in terms of muscle mass, muscle strength and performance.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 60
Healthy Volunteers: f
View:

• Subjects aged 60 years or above

• Subjects failed in AWGS algorithm

‣ skeletal muscle mass by BIA (male at \<7.0 kg/m\^2, female at \<5.7 kg/m\^2), and

⁃ handgrip strength (male at \<28 kg, female at \<18kg), and/or

⁃ gait speed test (\>1m/s)

Locations
Other Locations
Hong Kong Special Administrative Region
Evangelical Luthera Church Social Service - Hong Kong
ACTIVE_NOT_RECRUITING
Hong Kong
The Chinese University of Hong Kong Jockey Club Centre for Osteoporosis Care and Control
RECRUITING
Hong Kong
The Chinese University of Hong Kong, Department of Orthopaedics and Traumatology, 1/F Li Ka Shing Outpatient Clinic (North), PWH
RECRUITING
Hong Kong
Contact Information
Primary
Wing Hoi Cheung, PhD
louischeung@cuhk.edu.hk
35052715
Backup
Meng Chen Michelle Li, PhD
michellemcli@cuhk.edu.hk
35053312
Time Frame
Start Date: 2023-01-12
Estimated Completion Date: 2025-09
Participants
Target number of participants: 200
Treatments
Placebo_comparator: Control Group
Subjects assigned to Contro Group will not receive VT or HMB. They will receive daily protein supplement for 6 months.
Active_comparator: HMB only Group
Subjects assigned to HMB only Group will receive HMB supplement at 3g/day and daily protein supplement for 6 months.
Active_comparator: VT only Group
Subjects assigned to VT only Group will receive VT (0.3g, 35Hz, at least 3 times/week) and daily protein supplement for 6 months
Experimental: HMB + VT Group
Subjects assigned to HMB + VT Group will receive HMB supplement at 3g/day, VT at least 3 times/week and daily protein supplement for 6 months.
Related Therapeutic Areas
Sponsors
Leads: Chinese University of Hong Kong
Collaborators: Abbott

This content was sourced from clinicaltrials.gov