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Endurance Training in Patients Undergoing Lung Transplantation

Endurance Training in Patients Undergoing Lung Transplantation: Differences Between Treadmill and Cycle Ergometry Training

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04244305
Enrollment
80
Registered
2020-01-28
Start date
2016-05-01
Completion date
2020-05-01
Last updated
2020-01-29

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

Conditions

Lung Transplantation

Keywords

Exercise Therapy, Physical Therapy Modalities, Functional Capacity

Brief summary

Lung Transplantation is usually the last option for patients with chronic respiratory conditions in the late stages of the disease. Pulmonary rehabilitation and, particularly, endurance training, is a cornerstone in the management of these patients both during the pre-operative as well as the post-operative period as it improves cardiopulmonary fitness, muscle mass, muscle strength, health-related quality of life and potentially, survival. However, very few studies have been published addressing which modality of training, intensity, frequency or duration of training provides the best possible results in these patients. Therefore, the objective of this study was to compare two training modalities (treadmill walking versus cycle-ergometry) on functional capacity, muscle strength and lung function.

Interventions

OTHERExercise Therapy

Endurance training in the form of treadmill/cycle-ergometry

Sponsors

University Hospital A Coruña
Lead SponsorOTHER

Study design

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

Masking description

Assessors were blinded to group allocation of the participants

Eligibility

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

Inclusion criteria

* Patients undergoing lung transplantation at the Thoracic Surgery Unit of the Hospital Clínico Universitario de A Coruña. * Adults \> 18 years. * Ability to attend post-surgery exercise training for a minimum period of one month. * Sign informed consent.

Exclusion criteria

* Torpid post-operative recovery with a prolonged stay at the Post-Anaesthesia Care Unit \> 12 days. * Diagnosed with intensive care unit acquired muscle weakness.

Design outcomes

Primary

MeasureTime frameDescription
6 Minute Walk Test1 monthDistance covered during the 6 Minute Walk Test performed according to the American Thoracic Guidelines.

Secondary

MeasureTime frameDescription
Maximal isometric strength1 and 3 monthsIsometrical maximal strength of the brachial biceps and quadriceps muscle of both dominant and non-dominant limbs. Maximal isometric strength will be assessed using a hand-held dynamometer (Lafayette Instrument, Model 01165) and will be presented in kilograms
Sit-to-stand1 and 3 monthsNumber of times the patient can stand up from a chair and sit back in 30 seconds
Forced Expiratory Volume 1st second (FEV1)1 and 3 monthsChanges in Forced Expiratory Volume in the 1st second assessed during a forced spirometry test performed according to the international guidelines.
6 Minute Walk Test3 MonthsDistance covered with the 6 Minute Walk Test performed according to the American Thoracic Guidelines.
Maximal inspiratory and expiratory pressures1 and 3 monthsMaximal inspiratory and expiratory pressures performed with the respiratory muscles
Forced Expiratory Capacity (FVC)1 and 3 monthsChanges in forced expiratory capacity assessed during a forced spirometry test performed according to the international guidelines.
Peak Expiratory Flow (PEF)1 and 3 monthsChanges in peak expiratory flow assessed during a forced spirometry test performed according to the international guidelines.
Incremental Symptom-Limited Test1 and 3 monthsIncremental symptom-limited test performed on a cycle-ergometry with a 5-10W increase per minute up to maximal tolerance. Patient was monitorised during the test for both heart rate and oxygen saturation.

Outcome results

None listed

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