The objective of the first year is to collect limb occlusion pressure (LOP) measurements in older adults with varying levels of muscle health, which will serve as foundational data for subsequent investigations on blood flow restriction (BFR) combined with resistance training in individuals with dynapenia. This phase aims to examine LOP values and their potential influencing factors, including demographic and physiological characteristics such as age, height, body weight, blood pressure, waist circumference, body fat percentage, medical history of chronic diseases, and habitual physical activity. Muscle-related assessments will include skeletal muscle mass, thigh and calf circumference, handgrip strength, and lower limb muscle strength. Functional performance will be evaluated using the five-times sit-to-stand test and the SARC-F questionnaire for sarcopenia risk screening. LOP of the lower limbs will be measured using a BFR cuff system combined with a laboratory-developed blood flow detection device. The study will further investigate whether LOP values are associated with the aforementioned factors. The objective of the second year is to utilize high-density surface electromyography (dEMG) to analyze the electrophysiological characteristics of muscle contraction in individuals with sarcopenia under varying BFR pressures and resistance intensities. This includes examining motor unit recruitment patterns and recruitment thresholds, with the goal of identifying effective and appropriate BFR exercise parameters for this population. The objective of the third year is to investigate the effects of lower limb BFR combined with resistance training on functional performance in individuals with dynapenia. Building upon the findings from the first year, this phase will implement BFR resistance training interventions and evaluate both short-term and long-term effects. Through an experimental design, the study will assess changes in body composition, muscle strength, and functional performance following a four-month intervention, along with a three-month follow-up period, to determine whether participants can improve to a healthy status and maintain these improvements over time.
Age range
55 Years – 85 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Baseline Data
Timeframe: week0(pre-intervention), week16(post-intervention)
Muscle Strength
Timeframe: week0(pre-intervention), week16(post-intervention)
Muscle Function: The Short Physical Performance Battery (SPPB)
Timeframe: week0(pre-intervention), week16(post-intervention)
Height
Timeframe: week0(pre-intervention), week16(post-intervention)
Weight
Timeframe: week0(pre-intervention), week16(post-intervention)
BMI
Timeframe: week0(pre-intervention), week16(post-intervention)
Blood Pressure
Timeframe: week0(pre-intervention), week16(post-intervention)
LIN C Y Kaohsiung Medical University, Master
Circumferences
Timeframe: week0(pre-intervention), week16(post-intervention)
SARC-F Questionnaire
Timeframe: week0(pre-intervention)
Electromyography(EMG)
Timeframe: week0(pre-intervention), week16(post-intervention)
Limb Occlusion Pressure(LOP)
Timeframe: week0(pre-intervention)
Skeletal muscle mass
Timeframe: week0(pre-intervention), week16(post-intervention)
Body fat percentage
Timeframe: week0(pre-intervention), week16(post-intervention)
Estimated appendicular skeletal muscle mass
Timeframe: week0(pre-intervention), week16(post-intervention)