An assessment of patient outcomes following a rehabilitation programme for patients who have received heart/lung or lung transplant - a randomised controlled pilot trial
| ISRCTN | ISRCTN55416565 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN55416565 |
| Secondary identifying numbers | N0201139562 |
- Submission date
- 30/09/2004
- Registration date
- 30/09/2004
- Last edited
- 28/02/2018
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Surgery
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year
Plain English summary of protocol
Not provided at time of registration
Contact information
Ms Anne McDermott
Scientific
Scientific
Transplant Unit
Royal Brompton & Harefield NHS Trust
Harefield Hospital
Hill End Road
Harefield
UB9 6JH
United Kingdom
| Phone | +44 (0)1895 828676 |
|---|---|
| a.mcDermott@rbh.nthames.nhs.uk |
Study information
| Study design | Randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Hospital |
| Study type | Quality of life |
| Participant information sheet | Not available in web format, please use the contact details below to request a patient information sheet |
| Scientific title | An assessment of patient outcomes following a rehabilitation programme for patients who have received heart/lung or lung transplant - a randomised controlled pilot trial |
| Study objectives | Does the undertaking of a multidisciplinary-led programme of rehabilitation facilitate a better Quality of Life than a document-based rehabilitation programme in lung and or heart/lung transplant out-patients? |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Surgery: Heart/lung transplant |
| Intervention | Some patients will receive document packs while some will receive a multidisciplinary-led programme of rehabilitation. |
| Intervention type | Procedure/Surgery |
| Primary outcome measure | Not provided at time of registration |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/07/2004 |
| Completion date | 30/06/2005 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Both |
| Target number of participants | 20 |
| Key inclusion criteria | 20 patients |
| Key exclusion criteria | Does not meet inclusion criteria |
| Date of first enrolment | 01/07/2004 |
| Date of final enrolment | 30/06/2005 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Harefield Hospital
Harefield
UB9 6JH
United Kingdom
UB9 6JH
United Kingdom
Sponsor information
Department of Health
Government
Government
Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom
| Website | http://www.dh.gov.uk/Home/fs/en |
|---|
Funders
Funder type
Hospital/treatment centre
Royal Brompton and Harefield NHS Trust (UK)
No information available
Results and Publications
| Intention to publish date | |
|---|---|
| Individual participant data (IPD) Intention to share | No |
| IPD sharing plan summary | Not provided at time of registration |
| Publication and dissemination plan | Not provided at time of registration |
| IPD sharing plan |
Editorial Notes
28/02/2018: No publications found, verifying study status with principal investigator.
26/01/2016: no publications found on PubMed.
