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Low-load Blood Flow Restriction Training in COPD

Low-load Blood Flow Restriction Training in COPD

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04151771
Acronym
LL-BFRT COPD
Enrollment
30
Registered
2019-11-05
Start date
2019-12-27
Completion date
2023-01-28
Last updated
2023-04-12

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

Conditions

COPD, Muscle Weakness

Keywords

blood flow restriction training, pulmonary rehabilitation, COPD, muscle weakness

Brief summary

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.

Interventions

The intervention group will perform the exercises of the lower limbs using LL-BFRT with an occlusion pressure of 70% of arterial occlusion pressure with low training loads (30% of the 1 repetition maximum).

OTHERUsual outpatient pulmonary rehabilitation

The control group will perform outpatient pulmonary rehabilitation as established.

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Knee extensor strengthduring 12 weeks (24 exercise sessions)Between-group difference in total change in isometric muscle strength of the knee extensor muscles, measured by handheld dynamometry in newtonmeter

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026