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Pulmonary Rehabilitation in Patients Before Lung Transplantation (LTx)

S

Schön Klinik Berchtesgadener Land

Status

Completed

Conditions

Hypercapnia
Respiratory Insufficiency
Pre-Lung-Transplantation
COPD

Treatments

Other: interval training
Other: continuous endurance training

Study type

Interventional

Funder types

Other

Identifiers

NCT00962078
PRÄ-LTX-08022
Nr. 08022
Landesärztekammer Bayern
Ethikkommission

Details and patient eligibility

About

The purpose of this study is to study the effects of a complex pulmonary rehabilitation program on mobility measured by 6 minute walking distance (6MWD) and physical activity, measured via Dynaport and Actibelt Aktivitätsmonitor, dyspnoea (VAS), quality of life (HRQL (SF36, EuroQul)), anxiety and depression (HADS)and PaCO2-behavior under physical activity.

Enrollment

71 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • pre-LTx (listed for lung-transplantation or currently undergoing evaluation)
  • COPD Stadium IV GOLD
  • α-1-Antitrypsin-deficiency-Emphysema
  • respiratory Insufficiency
  • oxygen therapy (LTOT)

Exclusion criteria

  • serious Exacerbation (Symptoms longer than three days, change of therapy, e.i. antibiotics, steroids) during the last four weeks before rehabilitation
  • clinical signs of manifest heart insufficiency
  • acute coronar syndrome
  • left heart insufficiency(EF < 40%)
  • missing Compliance

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

71 participants in 2 patient groups

interval training
Other group
Description:
interval training in lung transplant candidates
Treatment:
Other: interval training
Continuous Training
Other group
Description:
continuous training in lung transplant candidates
Treatment:
Other: continuous endurance training

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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