ENhancing DElivery And outcomes of VOcational Rehabilitation

ISRCTN ISRCTN71943786
DOI https://doi.org/10.1186/ISRCTN71943786
Secondary identifying numbers 6104
Submission date
18/06/2010
Registration date
18/06/2010
Last edited
27/05/2014
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Mental and Behavioural Disorders
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English summary of protocol

Not provided at time of registration

Contact information

Prof Tom Craig
Scientific

Institute Of Psychiatry
16 De Crespigny Park
London
SE5 8AF
United Kingdom

t.craig@iop.kcl.ac.uk

Study information

Study designMulticentre randomised interventional treatment trial
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Hospital
Study typeTreatment
Participant information sheet Not available in web format, please use the contact details below to request a patient information sheet
Scientific titleEnhancing delivery and outcomes of vocational rehabilitation (ENDEAVOR): improving outcomes for young people with a first episode psychosis
Study acronymENDEAVOR
Study objectivesPrimary hypothesis:
To compare the effectiveness of two vocational rehabilitation interventions in helping people attain and retain employment following a first episode of psychosis.

Secondary hypothesis:
To describe the pathways,barriers and facillitators to employment in a cohort of people suffering a first episode psychosis.
Ethics approval(s)Charing Cross Research Ethics Committee approved on the 15th December 2008 (ref: 08/H0711/136)
Health condition(s) or problem(s) studiedTopic: Mental Health Research Network; Subtopic: Psychosis; Disease: Schizophrenia
Intervention1. Supported employment
2. Return to employment/eduation after first episode psychosis

Study entry: single randomisation only
Intervention typeOther
Primary outcome measureEmployment status, measured at 12 months
Secondary outcome measuresMeasured at 12 months:
1. Employment and education/training across follow up; qualifications obtained
2. Positive and Negative Symptom Scale (PANSS)
3. Global Assessment of Function
4. Time Budget
5. Client Service Receipt Inventory
Overall study start date01/06/2009
Completion date30/09/2011

Eligibility

Participant type(s)Patient
Age groupAdult
Lower age limit18 Years
Upper age limit35 Years
SexBoth
Target number of participantsPlanned sample size: 200; UK sample size: 200
Key inclusion criteria1. First episode psychosis
2. Aged 18 - 35 years, either sex
Key exclusion criteria1. Organic disease
2. Unable to comprehend written English
3. Unable to give informed consent
Date of first enrolment01/06/2009
Date of final enrolment30/09/2011

Locations

Countries of recruitment

  • England
  • United Kingdom

Study participating centre

Institute Of Psychiatry
London
SE5 8AF
United Kingdom

Sponsor information

Kings College London (KCL) (UK)
University/education

Institute of Psychiatry
Department of Psychology
Henry Wellcome Building
Box PO77, 16 De Crespigny Park
London
SE5 8AF
England
United Kingdom

http://www.iop.kcl.ac.uk/
ROR logo https://ror.org/0220mzb33

Funders

Funder type

Government

National Institute for Health Research (NIHR) (UK) - Research for Patient Benefit (RfPB) programme

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 01/08/2014 Yes No
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