A randomised study of pre-operative assessment and discharge planning
| ISRCTN | ISRCTN43091101 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN43091101 |
| Secondary identifying numbers | 9502057 R120/05272 RRD/7/1/2/1195 |
- Submission date
- 23/01/2004
- Registration date
- 23/01/2004
- Last edited
- 24/10/2019
- 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
Dr S Bond
Scientific
Scientific
CHSR
21 Claremont Place
Newcastle University
Newcastle upon Tyne
NE2 4AA
United Kingdom
Study information
| Study design | Randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Not specified |
| Study type | Not Specified |
| Participant information sheet | Not available in web format, please use the contact details below to request a patient information sheet |
| Scientific title | A randomised study of pre-operative assessment and discharge planning |
| Study objectives | A single-site preliminary randomised study comparing a pre-admission clinic and nurse practitioner intervention for surgical patients aged 65 years and above with standard care. The nurse practitioner intervention will involve assessment of informational, nutritional, functional and social needs and mobilisation of appropriate pre-admission and post-discharge services. |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Surgery |
| Intervention | 1. Nurse practitioner intervention 2. Standard care |
| Intervention type | Procedure/Surgery |
| Primary outcome measure | Outcomes related to health and social status, satisfaction with discharge and service provision, length of hospital stay, service use and costs will be ascertained up to 3 months post-operatively. |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 08/01/1995 |
| Completion date | 31/08/1997 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Senior |
| Sex | Both |
| Target number of participants | Not provided at time of registration |
| Key inclusion criteria | Surgical patients aged >65 years |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 08/01/1995 |
| Date of final enrolment | 31/08/1997 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
CHSR
Newcastle upon Tyne
NE2 4AA
United Kingdom
NE2 4AA
United Kingdom
Sponsor information
NHS R&D Regional Programme Register - Department of Health (UK)
Government
Government
The Department of Health
Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom
| Phone | +44 (0)20 7307 2622 |
|---|---|
| dhmail@doh.gsi.org.uk | |
| Website | http://www.doh.gov.uk |
Funders
Funder type
Government
NHS Executive Northern and Yorkshire (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
24/10/2019: No publications found. All search options exhausted.
