Low Load Blood Flow Restriction Resistance Training in Colorectal Cancer Related Sarcopenia
Sponsor: Ahmed Adel Ahmed Elsayed Ali Radwan • ClinicalTrials.gov ID: NCT07874035
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PURPOSE: To investigate the effects of low-load resistance training combined with blood flow restriction on muscle strength, functional performance, and cancer-related fatigue in colorectal cancer survivors with probable sarcopenia. BACKGROUND: Muscle weakness and cancer-related fatigue are prevalent in colorectal cancer survivors with probable sarcopenia and are associated with adverse outcomes. High-load resistance training is often poorly tolerated in this population. Although low-load resistance training with blood flow restriction shows promise, colorectal cancer-specific randomized evidence remains limited. HYPOTHESES: It is hypothesized that low-load blood flow restriction resistance training will lead to significant improvements in muscle strength and functional performance and a significant reduction in cancer-related fatigue in colorectal cancer survivors with probable sarcopenia. RESEARCH QUESTION: Does low-load blood flow restriction resistance training lead to significant improvements in muscle strength and functional performance and a significant reduction in cancer-related fatigue in colorectal cancer survivors with probable sarcopenia?
Interventions
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Low load blood flow restriction resistance training
(Behavioral)
Low-load resistance training combined with blood flow restriction using pneumatic cuffs applied to the proximal lower limb at 60% arterial occlusion pressure. Resistance exercise is performed at 30% of one-repetition maximum (1RM), using 30-15-15-15 repetitions with 30-60 seconds of rest between sets. The intervention is supervised twice weekly for 12 weeks.
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Low load resistance training without Blood Flow Restriction
(Behavioral)
Low-load resistance training without blood flow restriction. Resistance exercise is performed at 30% of one-repetition maximum (1RM), using 30-15-15-15 repetitions with 30-60 seconds of rest between sets. The intervention is supervised twice weekly for 12 weeks.
Eligibility criteria
Conditions
Locations
- Private Clinics — Cairo, Egypt
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Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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