A randomised controlled trial to compare the effectiveness and cost effectiveness of the hospital at home scheme with the acute hospital

ISRCTN ISRCTN76045614
DOI https://doi.org/10.1186/ISRCTN76045614
Secondary identifying numbers C/INT/16-04-94/COAST/F
Submission date
23/01/2004
Registration date
23/01/2004
Last edited
09/12/2010
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Other
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English summary of protocol

Not provided at time of registration

Contact information

Dr Joanna Coast
Scientific

University of Bristol
Department of Social Medicine
Canynge Hall
Whiteladies Road
Bristol
BS8 2PR
United Kingdom

Phone +44 (0)117 928 7337
Email jo.coast@bristol.ac.uk

Study information

Study designRandomised controlled trial
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Not specified
Study typeQuality of life
Scientific title
Study objectivesTo compare effectiveness and acceptability of early discharge to a hospital at home scheme with that of routine discharge from acute hospital.
Ethics approval(s)Not provided at time of registration
Health condition(s) or problem(s) studiedQuality of life
InterventionPatients' received hospital at home care or routine hospital care.
Intervention typeOther
Primary outcome measurePatients' quality of life, satisfaction, and physical functioning assessed at 4 weeks and 3 months after randomisation to treatment; length of stay in hospital and in hospital at home scheme after randomisation; mortality at 3 months.
Secondary outcome measuresNot provided at time of registration
Overall study start date01/06/1994
Completion date31/07/1996

Eligibility

Participant type(s)Patient
Age groupNot Specified
SexNot Specified
Target number of participants241
Key inclusion criteria241 hospitalised but medically stable elderly patients who fulfilled criteria for early discharge to hospital at home scheme and who consented to participate.
Key exclusion criteriaNot provided at time of registration
Date of first enrolment01/06/1994
Date of final enrolment31/07/1996

Locations

Countries of recruitment

  • England
  • United Kingdom

Study participating centre

University of Bristol
Bristol
BS8 2PR
United Kingdom

Sponsor information

NHS R&D Regional Programme Register - Department of Health (UK)
Government

The Department of Health
Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom

Phone +44 (0)20 7307 2622
Email dhmail@doh.gsi.org.uk
Website http://www.doh.gov.uk

Funders

Funder type

Government

NHS Executive South West (UK)

No information available

Results and Publications

Intention to publish date
Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
Publication and dissemination planNot provided at time of registration
IPD sharing plan

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Results article results 13/06/1998 Yes No