ISRCTN ISRCTN06481116
DOI https://doi.org/10.1186/ISRCTN06481116
Protocol serial number 11278
Sponsor Queen Mary, University of London (UK)
Funder NIHR (UK) - Research for Patient Benefit (RfPB) RfPB PB-PG-0110-21014
Submission date
25/04/2013
Registration date
26/04/2013
Last edited
09/06/2016
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

Prof Graham Foster
Scientific

Institute of Cell and Molecular Science
Medical College
Turner Street
London
E1 2AD
United Kingdom

Phone +44 20 7882 2483
Email g.r.foster@qmul.ac.uk

Study information

Primary study designInterventional
Study designInterventional randomised open label controlled clinical trial; Design type: Process of Care, Treatment
Secondary study designRandomised controlled trial
Scientific titleDischarge planning for the homeless, examining The London Pathway. Does a GP led discharge team reduce the inpatient burden and improve quality of care?
Study objectivesThe London Pathway model of care for people who are homeless improves the quality of care and reduces overall length of hospital stay.

http://public.ukcrn.org.uk/search/StudyDetail.aspx?StudyID=11278
Ethics approval(s)London South East ethics committee, ref:11/LO/0755
Health condition(s) or problem(s) studiedTopic: Primary Care Research Network for England, Oral and Gastrointestinal, Generic Health Relevance and Cross Cutting Themes; Subtopic: Oral and Gastrointestinal (all Subtopics), Generic Health Relevance (all Subtopics); Disease: All Diseases, Hepatology, Health Services Research
InterventionRandomised trial of enhanced vs normal care for people who are homeless.

GP assisted care, GP to assist in management

Follow Up Length: 6 months
Intervention typeOther
Primary outcome measure(s)

Length of stay; Timepoint: Duration of in-patient stay

Key secondary outcome measure(s)

Not provided at time of registration

Completion date30/06/2013

Eligibility

Participant type(s)Patient
Age groupAdult
Lower age limit18 Years
Upper age limit100 Years
SexAll
Target sample size at registration800
Key inclusion criteria1. People admitted to one of the hospitals involved in the study who do not have a home of their own where they usually sleep at night
2. Male & Female, Lower Age Limit 18 years, Upper Age Limit 100 years
Key exclusion criteria1. Unwilling or unable to provide informed consent
2. Temporarily homeless (defined as likely to be without accommodation for less than 2 weeks)
Date of first enrolment01/12/2011
Date of final enrolment30/06/2013

Locations

Countries of recruitment

  • United Kingdom
  • England

Study participating centre

Institute of Cell and Molecular Science
London
E1 2AD
United Kingdom

Results and Publications

Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
IPD sharing plan

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Results article results 01/06/2016 Yes No

Editorial Notes

09/06/2016: Publication reference added.