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Bloodflow Restricted Exercise in Healthy Ageing

Bloodflow Restricted Exercise in Healthy Ageing

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04712955
Enrollment
24
Registered
2021-01-19
Start date
2021-01-19
Completion date
2025-07-01
Last updated
2021-01-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aging

Keywords

bloodflow restricted exercise, skeletal muscle, muscle stem cells

Brief summary

The overall objective of this study is to investigate the efficacy of low-intensity blood flow restricted resistance exercise (BFRRE) to promote health beneficial skeletal muscle adaptations and augment muscle function in a healthy older population. This objective will be achieved by in-dept evaluation of skeletal muscle cellular and functional characteristics prior to and after an intervention period comprising 6 weeks of BFRRE or non-exercise control intervention in healthy older subjects. A special focus is placed on the ability of BFRRE to stimulate skeletal muscle protein synthesis and augment muscle stem cell function. Furthermore, recent findings suggests that similar exercise interventions in a population of patients with heart failure (HF) does not stimulate the desired adaptations. In accordance, we aim to compare the adaptive response to BFRRE amongst HF patients and the enrolled age-matched healthy individuals from the present investigation. The findings of the current study will expand our understanding of how low-intensity resistance exercise alternatives might be viable in promoting muscle anabolism to combat the loss of muscle mass observed with ageing as well as the potential anabolic resistance accompanying HF diagnosis.

Interventions

OTHERBloodflow restricted exercise

Low-intensity bloodflow restricted resistance exercise is conducted as traditional knee extension exercise with a load corresponding to 30% of 1 repetition maximum (RM), with concurrent partial occlusion of the circulation by means of inflatable pneumatic cuffs wrapped around the proximal part of the thighs. Cuffs are inflated to a pressure corresponding to 50% of the arterial occlusion pressure, which only compromises venous but not arterial blood flow.

Sponsors

University of Aarhus
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

Single center randomised controlled trial.

Eligibility

Sex/Gender
ALL
Age
45 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Able to understand the written and spoken information and to give informed consent for inclusion. * Age between 45 and 80 years * Able to sit in a knee extension machine * Able to deliver muscle biopsies * Able to train 3 times per week during a 6-week period

Exclusion criteria

* Known history of cardiac disease * Habitual exercise with high intensity \> 2 times pr. week within the past 6 months * Pregnancy * Diabetes mellitus * Peripheral neuropathy * Dialysis treatment * Severe peripheral arterial disease * Concomitant acute life threatening medical condition * Intracranial aneurisms, arteriovenous malformation, cerebral neoplasm or abscess * Severe arterial hypertension (≥ 180/≥ 110 mmHg) or moderate arterial hypertension (160-179/100-109) despite medical treatment * Moderate or severe chronic obstructive pulmonary disease * Decreased kidney function - eGFR \< 60 ml/min

Design outcomes

Primary

MeasureTime frameDescription
Subfractional muscle protein synthesis rates6 weeksMyofibrillar protein synthesis rate
Segmental muscle mass of lower extremity6 weeksDual Energi X-ray Absorption (DEXA)
Muscle fibre cross sectional area (CSA)6 weeksHistological examination of muscle biopsies
Muscle stem cell function6 weeksTime to first division

Secondary

MeasureTime frameDescription
1 repetition maximum6 weeksDynamic muscle strength
Muscle strength-endurance capacity6 weeksLocal muscle endurance
Maximal Voluntary Contraction (MVC)6 weeksIsometric muscle function

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026