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Clinical Trials/NCT05734534
NCT05734534
Recruiting
Not Applicable

Effects of BFR Interventions on Muscle Function and Adaptations in Healthy Individuals and Individuals With COPD

Morten Hostrup, PhD1 site in 1 country105 target enrollmentMarch 1, 2023
ConditionsHealthyCOPD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy
Sponsor
Morten Hostrup, PhD
Enrollment
105
Locations
1
Primary Endpoint
Muscle strength
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

The purpose of the study is to investigate the effect of different blood flow restriction (BFR) interventions on muscle function and adaptations both in healthy well-trained individuals and individuals diagnosed with COPD.

Registry
clinicaltrials.gov
Start Date
March 1, 2023
End Date
August 1, 2024
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Morten Hostrup, PhD
Responsible Party
Sponsor Investigator
Principal Investigator

Morten Hostrup, PhD

Associate Professor

University of Copenhagen

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Muscle strength

Time Frame: Change assessed from before to after the intervention (6 weeks in study A, on average 7 days in study B)

Maximal voluntary isometric contraction of m. quadriceps femoris

Secondary Outcomes

  • Maximal oxygen consumption(Change assessed from before to after the 6 week intervention)
  • Skeletal muscle mitochondrial respiration(Change assessed from before to after the intervention (6 weeks in study A, on average 7 days in study B))
  • Fiber cross-sectional area(Change assessed from before to after the intervention (6 weeks in study A, on average 7 days in study B))
  • Functional exercise capacity(Change assessed from before to after the 6 week intervention (only in individuals with COPD))
  • Satellite cells(Change assessed from before to after the intervention (6 weeks in study A, on average 7 days in study B))
  • Lean mass(Change assessed from before to after the 6 week intervention)
  • Myonuclei(Change assessed from before to after the intervention (6 weeks in study A, on average 7 days in study B))

Study Sites (1)

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