Actively Recruiting
Combined Exercise and Nutrition Intervention for Sarcopenia
Led by Seoul Bumin Hospital · Updated on 2024-10-24
118
Participants Needed
1
Research Sites
144 weeks
Total Duration
On this page
Sponsors
S
Seoul Bumin Hospital
Lead Sponsor
N
National Evidence-Based Healthcare Collaborating Agency
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study aims to demonstrate the effect of combined exercise-nutrition intervention in old adults with sarcopenia. This study will be conducted with prospectively randomized controlled trial comparing outcome of combined exercise-nutrition intervention with conventional medical care. Handgrip strength, gait speed, knee extensor muscle power, physical performance, muscle mass using DEXA, quality of life, activities of daily living, sarcopenia screening questionnaire, nutritional assessment will be evaluated on baseline, 12-weeks and 24-weeks after intervention
CONDITIONS
Official Title
Combined Exercise and Nutrition Intervention for Sarcopenia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients older than 65 years and under 90 years
- Patients who meet the criteria for the Asian Working Group for Sarcopenia (AWGS) 2019
- Patients who had metabolic syndrome
You will not qualify if you...
- Patients with estimated glomerular filtration rate (eGFR) less than 30
- Patients with musculoskeletal or chronic lung disease incapable of exercise
- Patients with untreated or uncontrolled cardiovascular disease affecting muscle mass or exercise ability
- Patients less than 5 years after treatment of malignant tumor
- Patients with liver cirrhosis, diabetes, or other chronic diseases
- Patients unable to perform combined exercise nutrition intervention for other reasons
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Seoul Bumin Hospital
Seoul, South Korea, 07590
Actively Recruiting
Research Team
Y
Yongchan Ha, phD
CONTACT
E
Eunsuk Kim, bachelor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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