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An exploratory randomised trial of the effectiveness of a training intervention delivered to staff of a district nursing service in improving the knowledge and detection of common mental disorders in a mixed adult and older adult caseload
Source of recordUK Trials
ISRCTNISRCTN91170552
Date ISRCTN assigned03/02/2003
Local reference number(s)G84/6075
Public titleAn exploratory randomised trial of the effectiveness of a training intervention delivered to staff of a district nursing service in improving the knowledge and detection of common mental disorders in a mixed adult and older adult caseload
Scientific title
AcronymN/A
Disease/condition/study domainMental and Behavioural Disorders
Study hypothesisTo ascertain whether a training programme delivered to district nurses and associated health workers can produce significant and sustained improvements in their abilities to detect cases of clinically significant psychological disorder in their patients.
Design/methodologyRandomised controlled trial
Research ethics reviewNot provided at time of registration
Countries of trialUnited Kingdom
Participants - inclusion criteria1. All consenting state qualified nursing staff will be included, home care staff (levels I & II) will be randomly selected
2. Patients on their caseloads aged over 18, who provide consent, will be included
Participants - exclusion criteriaFor patients, diagnoses of: severe mental illness; current substance misuse disorder; moderate or severe organic brain disorder.
Patient information material
Anticipated start date30/09/2002
Anticipated end date29/09/2005
Status of trialCompleted
Target number of participants115 staff, 900 patients
InterventionsA training package comprising seven sessions will be developed based upon evidence-based clinical practice guidelines and existing teaching resources. This will be delivered utilising varied learning approaches, predominantly interactive educational workshops such as those involving small group discussion or case studies, to a randomly allocated group of staff.

In a second phase one year later, the training intervention will be delivered to the prior control group.
Primary outcome measure(s)Changes in measures of case recognition utilising standard properties of diagnostic instruments will be compared between intervention and control groups pre- and post-intervention, and at 12 months. Included patients will complete Hospital Anxiety Depression Scale (Zigmond & Snaith, 1983), those over 65 will additionally complete the Short Geriatric Depression Scale (15) (Sheik & Yesavage, 1986). Staff will concurrently complete a five-point measure of presence and severity of mental disorder for their patients. Staff knowledge and attitudes will be measured at baseline and at three and 12 month intervals using an adapted version of the Depression Attitude Questionnaire (Botega, Blizard, Wilkinson, Mann, 1992), and multiple choice questions based upon World Health Organisation (WHO) primary care mental health literature.
Secondary outcome measure(s)Not provided at time of registration
Sources of fundingMedical Research Council
Sponsor nameMedical Research Council (UK)
Sponsor details20 Park Crescent
London
United Kingdom
W1B 1AL
Sponsor telephone+44 (0)20 7636 5422
Sponsor fax+44 (0)20 7436 6179
Sponsor emailclinical.trial@headoffice.mrc.ac.uk
Sponsor websitehttp://www.mrc.ac.uk
Contact nameMr Mark Haddad
Contact detailsHealth Services Research Department
Institute of Psychiatry PO30
De Crespigny Park
Denmark Hill
London
United Kingdom
SE5 8AF
Contact telephone+44 (0)20 7848 0139
Contact fax+44 (0)20 7848 0458
Contact emailm.haddad@iop.kcl.ac.uk
More informationFor more up-to-date information please go to the ISRCTN link below.
Link to record in ISRCTN RegisterISRCTN91170552
Date last extracted from ISRCTN register17/04/2008
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