CASPER plus (CollAborative care in Screen-Positive EldeRs with major depressive disorder): Study protocol for a randomised controlled trial
Overend, Karen; Lewis, Helen; Bailey, Della; et al.Bosanquet, Kate; Chew-Graham, Carolyn; Ekers, D; Gascoyne, Samantha; Hems, Deborah; Holmes, John; Keding, Ada; McMillan, D; Meer, Shaista; Mitchell, Natasha; Nutbrown, Sarah; Parrott, Steve; Richards, David; Traviss, Gemma; Trepel, Dominic; Woodhouse, Rebecca; Gilbody, Simon
Date: 19 November 2014
Background: Depression accounts for the greatest disease burden of all mental health disorders, contributes heavily to healthcare costs, and by 2020 is set to become the second largest cause of global disability. Although 10% to 16% of people aged 65years and over are likely to experience depressive symptoms, the condition is under-diagnosed ...
Background: Depression accounts for the greatest disease burden of all mental health disorders, contributes heavily to healthcare costs, and by 2020 is set to become the second largest cause of global disability. Although 10% to 16% of people aged 65years and over are likely to experience depressive symptoms, the condition is under-diagnosed and often inadequately treated in primary care. Later-life depression is associated with chronic illness and disability, cognitive impairment and social isolation. With a progressively ageing population it becomes increasingly important to refine strategies to identity and manage depression in older people. Currently, management may be limited to the prescription of antidepressants where there may be poor concordance; older people may lack awareness of psychosocial interventions and general practitioners may neglect to offer this treatment option. Methods/design: CASPER Plus is a multi-centre, randomised controlled trial of a collaborative care intervention for individuals aged 65years and over experiencing moderate to severe depression. Selected practices in the North of England identify potentially eligible patients and invite them to participate in the study. A diagnostic interview is carried out and participants with major depressive disorder are randomised to either collaborative care or usual care. The recruitment target is 450 participants. Discussion: Results will add to existing evidence and a positive outcome may lead to the commissioning of this model of service in primary care. Trial registration: ISRCTN45842879 (24 July 2012).
Institute of Health Research
College of Medicine and Health
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