Alveolitis, Fibrosing, Bronchiectasis, Cystic Fibrosis, Emphysema, Lung Diseases
Conditions
Keywords
End Stage Fibrotic Lung Disease
Brief summary
At present, a specific community based rehabilitation programme for lung or heart-lung transplant recipients does not exist. 160 hospitals throughout the United Kingdom (UK) offer pulmonary rehabilitation programmes. The programmes operate under evidence-based guidelines as outlined by the Chartered Society of Physiotherapy. Increasing evidence shows that rehabilitation programmes help improve performance, exercise endurance, and quality of life; and reduce symptoms and demand on health-care resources. This study proposes to compare the outcomes of lung and heart-lung transplant patients attending local pulmonary rehabilitation against others receiving the Trust's current document-based programme. The study is a randomized controlled trial: * Control Arm: Those patients randomized to the 'control' arm will receive the Trust's standard rehabilitation programme that consists of an information pack supplied upon discharge. They will then complete and undertake the following tests: Short-Form 36 (SF 36; version 2) Questionnaire, Chronic Respiratory Questionnaire (CRQ-SR), Incremental Shuttle Walk Test and Spirometry forced expiratory volume in 1 second (FEV1) and forced vital capacity (FVC). The patient will follow the information contained in the information pack and the above tests and questionnaires will be repeated 6 months post discharge. * Experimental Arm: A patient who is randomized to the 'experimental' arm will be asked to complete the following tests upon discharge: Short-Form 36 (SF 36; version 2) Questionnaire, Chronic Respiratory Questionnaire (CRQ-SR), Incremental Shuttle Walk Test and Spirometry FEV1 and FVC. Three months post discharge, the patient will be enrolled into a local pulmonary rehabilitation programme. The programme is typically structured to last 6-12 weeks. The above tests and questionnaires will be repeated 6 months post discharge. To measure the effectiveness of either the information pack or the rehabilitation programme the following endpoints will be subjected to analysis in both the experimental and the control group: * Short-Form 36 Questionnaire; * Chronic Respiratory Questionnaire; * Incremental Shuttle Walk Test; * Borg Scale; * Spirometry FEV1 and FVC; * Hospital re-admission rates and mortality rates. The undertaking of a multidisciplinary-led programme of rehabilitation facilitates a better quality of life than a document-based rehabilitation programme in lung and or heart-lung transplant out-patients. The aim of the study is to construct an optimal programme of rehabilitation in lung or heart-lung patients.
Interventions
PROCEDUREPulmonary rehabilitation programme
Sponsors
Royal Brompton & Harefield NHS Foundation Trust
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* All patients who have undergone either a lung or heart-lung transplant. * Fit for discharge from the Transplant Unit's Intensive Care Unit. * \> 18 years of age.
Exclusion criteria
* Patients under 18 years of age. * Patients unable to understand or comprehend the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Exercise Shuttle Test (metres completed) | — |
Secondary
| Measure | Time frame |
|---|---|
| Borg score | — |
| Quality of life: SF-36 and Chronic Respiratory Questionnaires | — |
| Spirometry | — |
| Hospital re-admission rates | — |
| Organ rejection | — |
Countries
United Kingdom
Contacts
Primary ContactMICHAEL G PREEDY, BSc Econ
Backup ContactCHRISTOPHER THEAKER
Outcome results
None listed