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Can integrating the Memory Support Intervention into cognitive therapy improve depression outcome? Study protocol for a randomized controlled trial

The Memory Support Intervention was developed in response to evidence showing that: (1) patient memory for treatment is poor, (2) poor memory for treatment is associated with poorer adherence and poorer outcome, (3) the impact of memory impairment can be minimized by the use of memory support strate...

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Published in:Current controlled trials in cardiovascular medicine 2017-11, Vol.18 (1), p.539-539, Article 539
Main Authors: Harvey, Allison G, Dong, Lu, Lee, Jason Y, Gumport, Nicole B, Hollon, Steven D, Rabe-Hesketh, Sophia, Hein, Kerrie, Haman, Kirsten, McNamara, Mary E, Weaver, Claire, Martinez, Armando, Notsu, Haruka, Zieve, Garret, Armstrong, Courtney C
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cited_by cdi_FETCH-LOGICAL-c560t-37bb86c616d1cee64109d0db0e39503e1d75f0396f44363f92c661a0fbb23ead3
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creator Harvey, Allison G
Dong, Lu
Lee, Jason Y
Gumport, Nicole B
Hollon, Steven D
Rabe-Hesketh, Sophia
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Weaver, Claire
Martinez, Armando
Notsu, Haruka
Zieve, Garret
Armstrong, Courtney C
description The Memory Support Intervention was developed in response to evidence showing that: (1) patient memory for treatment is poor, (2) poor memory for treatment is associated with poorer adherence and poorer outcome, (3) the impact of memory impairment can be minimized by the use of memory support strategies and (4) improved memory for treatment improves outcome. The aim of this study protocol is to conduct a confirmatory efficacy trial to test whether the Memory Support Intervention improves illness course and functional outcomes. As a "platform" for the next step in investigating this approach, we focus on major depressive disorder (MDD) and cognitive therapy (CT). Adults with MDD (n = 178, including 20% for potential attrition) will be randomly allocated to CT + Memory Support or CT-as-usual and will be assessed at baseline, post treatment and at 6 and 12 months' follow-up (6FU and 12FU). We will compare the effects of CT + Memory Support vs. CT-as-usual to determine if the new intervention improves the course of illness and reduces functional impairment (aim 1). We will determine if patient memory for treatment mediates the relationship between treatment condition and outcome (aim 2). We will evaluate if previously reported poor treatment response subgroups moderate target engagement (aim 3). The Memory Support Intervention has been developed to be "transdiagnostic" (relevant to a broad range of mental disorders) and "pantreatment" (relevant to a broad range of types of treatment). This study protocol describes a "next step" in the treatment development process by testing the Memory Support Intervention for major depressive disorder (MDD) and cognitive therapy (CT). If the results are promising, future directions will test the applicability to other kinds of interventions and disorders and in other settings. ClinicalTrials.gov, ID: NCT01790919 . Registered on 6 October 2016.
doi_str_mv 10.1186/s13063-017-2276-x
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subjects Alzheimer's disease
Care and treatment
Chronic illnesses
Clinical trials
Cognition & reasoning
Cognitive therapy
Depression
Depression, Mental
Education
Experimental therapeutics
Intervention
Memory
Memory support
Mental depression
Mental disorders
Patients
Psychosis
Study Protocol
Transdiagnostic
title Can integrating the Memory Support Intervention into cognitive therapy improve depression outcome? Study protocol for a randomized controlled trial
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