PRIDE Trial: PRimary care Intervention for Depression in the Elderly

ISRCTN ISRCTN60361331
DOI https://doi.org/10.1186/ISRCTN60361331
Secondary identifying numbers 0250024
Submission date
09/03/2005
Registration date
26/05/2005
Last edited
16/09/2009
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

Dr Carolyn Chew-Graham
Scientific

Rusholme Academic Unit
Rusholme Health Centre
Walmer Street
Rusholme
Manchester
M14 5NP
United Kingdom

Email cchew@man.ac.uk

Study information

Study designRandomised controlled trial
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)GP practice
Study typeTreatment
Scientific titleA controlled trial to investigate the feasibility of a new model of intervention for the treatment of late-life depression in primary care
Study acronymPRIDE
Study objectivesThe aim of the trial is to test whether the new intervention, delivered in primary care, leads to improved outcomes for elderly depressed people.
Ethics approval(s)Not provided at time of registration
Health condition(s) or problem(s) studiedLate-life depression
InterventionThe intervention comprises: antidepressants (where appropriate) prescribed by the general practitioner, a brief psychological intervention delivered by a community psychiatric nurse (CPN) employed by the study, and care management according to a defined algorithm. The CPN is working closely with the patient's general practitioner but the model demands close support from and liaison with the specialist community mental health team for older people.

Control: usual care
Intervention typeOther
Primary outcome measureSCID scores
Secondary outcome measuresMontgomery-asberg scores
Overall study start date01/02/2004
Completion date30/09/2005

Eligibility

Participant type(s)Patient
Age groupSenior
SexBoth
Target number of participants100
Key inclusion criteriaElderly people (>60) with depression as defined by the GP or community or practice nurse are referred into the study.
If depressed (Geriatric Depression Scale [GDS] %) they are randomised to intervention or usual care group.
Key exclusion criteriaDoes not meet inclusion criteria
Date of first enrolment01/02/2004
Date of final enrolment30/09/2005

Locations

Countries of recruitment

  • England
  • United Kingdom

Study participating centre

Rusholme Academic Unit
Manchester
M14 5NP
United Kingdom

Sponsor information

University of Manchester (UK)
University/education

Oxford Road
Manchester
M13 9PL
England
United Kingdom

Email cchew@man.ac.uk
ROR logo "ROR" https://ror.org/027m9bs27

Funders

Funder type

Government

Department of Health (UK) (ref: 0250024) - the call for bids was 2002, National Service Framework for Older People

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 01/06/2006 Yes No
Results article results 01/05/2007 Yes No
Results article results 04/07/2007 Yes No