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Low-load Blood Flow Restriction Training in COPD (LL-BFRT COPD)

University of Zurich (UZH) logo

University of Zurich (UZH)

Status

Completed

Conditions

Muscle Weakness
COPD

Treatments

Other: Low-load blood flow restriction training
Other: Usual outpatient pulmonary rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT04151771
SNCTP000003509 (Other Identifier)
2019-01641 (Other Identifier)

Details and patient eligibility

About

Peripheral muscle weakness is a predominant problem in patients with COPD and treated using exercise training in pulmonary rehabilitation. Despite pulmonary rehabilitation being an effective intervention, muscle strength impairment is a persisting problem in COPD patients. Patients have problems to tolerate the high training loads, which are necessary to develop strength. Low-load blood flow restriction training (LL-BFRT) might therefore be an option to enhance muscular response of patients with COPD to strength training. Up to now, no studies investigating LL-BFRT in respiratory diseases are available.

The primary outcome of this randomized pilot study is knee extensor muscle strength. Secondary, the study will evaluate if LL-BFRT is well tolerated and feasible in COPD patients attending outpatient pulmonary rehabilitation.

Enrollment

30 patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosed COPD according to GOLD-guidelines
  • Assigned to outpatient pulmonary rehabilitation by the treating physician

Exclusion criteria

  • Physical or intellectual impairment precluding informed consent or protocol adherence
  • Non-German speaking (precluding informed consent)
  • Acute or recent (within the last 6 weeks) exacerbation of COPD
  • Attending a pulmonary rehabilitation program within the last 3 months
  • Pregnant patients
  • History of thromboembolic event in the lower extremity
  • Diagnosis of polyneuropathy
  • Resting systolic blood pressure <100 mmHg

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 2 patient groups

LL-BFRT group
Experimental group
Description:
Participants randomised into intervention group are attending pulmonary rehabilitation in which strengthening exercises of the lower limb are performed using LL-BFRT.
Treatment:
Other: Low-load blood flow restriction training
Usual pulmonary rehabilitation group
Active Comparator group
Description:
Participants randomised into control group are attending usual pulmonary rehabilitation as established.
Treatment:
Other: Usual outpatient pulmonary rehabilitation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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