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Study identifier: NCT06161402 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Elastic Band-Progressive Resistance Training (EB-PRT) for Sarcopenia Among Heart Failure Patients

Condition: Heart Failure  ·  Sponsor: The University of Hong Kong

PhaseNA
Planned participants62
Who can joinAll sexes, 50 Years to no upper limit
Healthy volunteersNo

About this study

Heart failure (HF) is a complicated clinical syndrome caused by structural and/or functional cardiac abnormalities that result in ineffective myocardial pumping. HF management has placed more emphasis on improving the prognostic factors which determine these poor clinical outcomes. More recently, the prognostic role of sarcopenia in HF has received particular attention. Defined as progressive and generalized decline in skeletal muscle mass, strength and physical performance due to aging, sarcopenia is definitely a common comorbid of HF which follows an age-specific disease epidemiology. Given muscle disuse is the most preventable and reversible factor of sarcopenia, more evidence points to the therapeutic value of resistance training (RT) for this debilitating condition. Nevertheless, the therapeutic effects of RT on improving sarcopenia and thereby the disease prognosis among HF patients is yet to be evaluated. Therefore, the sequential mixed method study including a pilot RCT will be conducted to evaluate the preliminary effect of a 14-week elastic band-progressive resistance training (EB-PRT) and a subsequent qualitative study to explore the subjects' engagement experience. The outcomes cover the whole set of defining characteristics including muscle mass, muscle strength and functional performance and the clinical outcomes which reflect HF disease severity and patient-reported HRQL.

This description comes directly from the study's public registry record.

Talk to the study team

Doris Sau Fung YU, PhD  ·  852 3817 6319  ·  dyu1@hku.hk

Always discuss trial participation with your own doctor first.

Locations (1)

The University of Hong KongHong Kong, Hong KongRecruiting

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Source record: clinicaltrials.gov/study/NCT06161402