Title of article :
A Stepwise Psychotherapy Intervention for Reducing Risk in Coronary Artery Disease (SPIRR-CAD) — Rationale and design of a multicenter, randomized trial in depressed patients with CAD
Author/Authors :
Albus، نويسنده , , Christian and Beutel، نويسنده , , Manfred E. and Deter، نويسنده , , Hans-Christian and Fritzsche، نويسنده , , Kurt and Hellmich، نويسنده , , Martin and Jordan، نويسنده , , Jochen and Juenger، نويسنده , , Jana and Krauth، نويسنده , , Christian and Ladwig، نويسنده , , Karl-Heinz and Michal، نويسنده , , Matthias and Mueck-Weymann، نويسنده , , Michael and Petrowski، نويسنده , , Katja and Pieske، نويسنده , , Burkert and Ronel، نويسنده , , Joram and Soellner، نويسنده , , Wolfgang and Waller، نويسنده , , Christiane and Weber، نويسنده , , Cora and Herrmann-Lingen، نويسنده , , Christoph، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
Pages :
8
From page :
215
To page :
222
Abstract :
Objective sive symptoms are highly relevant for the quality of life, health behavior, and prognosis in patients with coronary artery disease (CAD). However, previous psychotherapy trials in depressed CAD patients produced small to moderate effects on depression, and null effects on cardiac events. In this multicentre psychotherapy trial, symptoms of depression are treated together with the Type D pattern (negative affectivity and social inhibition) in a stepwise approach. s d women (N=569, age 18–75 years) with any manifestation of CAD and depression scores ≥ 8 on the Hospital Anxiety and Depression Scale (HADS), will be randomized (allocation ratio 1:1) into the intervention or control group. Patients with severe heart failure, acutely life-threatening conditions, chronic inflammatory disease, severe depressive episodes or other severe mental illness are excluded. Both groups receive usual medical care. Patients in the intervention group receive three initial sessions of supportive individual psychotherapy. After re-evaluation of depression (weeks 4–8), patients with persisting symptoms receive an additional 25 sessions of combined psychodynamic and cognitive–behavioral group therapy. The control group receives one psychosocial counseling session. Primary efficacy variable is the change of depressive symptoms (HADS) from baseline to 18 months. Secondary endpoints include cardiac events, remission of depressive disorder (SCID) and Type D pattern, health-related quality of life, cardiovascular risk profile, neuroendocrine and immunological activation, heart rate variability, and health care utilization, up to 24 months of follow-up (ISRCTN: 76240576; NCT00705965). Funded by the German Research Foundation.
Keywords :
Randomized controlled trial , Coronary Artery Disease , depression , psychotherapy
Journal title :
Journal of Psychosomatic Research
Serial Year :
2011
Journal title :
Journal of Psychosomatic Research
Record number :
1743666
Link To Document :
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