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Psychosocial/Behavioral Intervention in Post-Stroke Depression

Primary Purpose

Stroke

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Modified cognitive behavioral therapy plus problem-solving
usual care
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring Depressive symptoms, Behavior and behavior mechanisms, Recovery

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Ischemic stroke within previous 4 months Screens positive for depressive symptoms by Geriatric Depression Scale Able to provide informed consent - Exclusion Criteria: Subarachnoid or intracranial hemorrhagic stroke Global aphasia Reduced level of consciousness (GCS <15)

Sites / Locations

  • University of Washington

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

Nine session psychosocial/behavioral counseling with homework

Usual clinic care with booklet describing depression following stroke

Outcomes

Primary Outcome Measures

Reduction in depression (Hamilton Depression Rating Scale)at 12 months following stroke.

Secondary Outcome Measures

Reduction in limitations in activity (Barthel Index)6, 12, 24 months
Reduction in limitation in participation (Stroke Impact Scale)6, 12, 24 months
Overall stroke impact (Stroke Impact Scale)6,12,24 months post- stroke.

Full Information

First Posted
September 12, 2005
Last Updated
September 21, 2008
Sponsor
University of Washington
Collaborators
National Institute of Nursing Research (NINR)
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1. Study Identification

Unique Protocol Identification Number
NCT00194454
Brief Title
Psychosocial/Behavioral Intervention in Post-Stroke Depression
Official Title
Psychosocial/Behavioral Intervention in PSD
Study Type
Interventional

2. Study Status

Record Verification Date
September 2008
Overall Recruitment Status
Completed
Study Start Date
March 2002 (undefined)
Primary Completion Date
February 2008 (Actual)
Study Completion Date
February 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Washington
Collaborators
National Institute of Nursing Research (NINR)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary aim of this study is to determine the effect of a nurse-delivered psychosocial/behavioral intervention on reduction of depression in community dwelling post-stroke patients. We expect the combined behavioral and pharmacologic intervention to be more effective than pharmacotherapy alone in sustaining the improvement in depression for the experimental group. Secondary aims are to examine the effect of the psychosocial/behavioral intervention time course and sustainability of response to treatment, effect on limitations in ability, limitation in participation and overall stroke impact in community-dwelling post-stroke patients, and to compare ischemic stroke survivors who are and are not depressed within the first four months following stroke by their 5-HTTLPR genotypes (s/s, s/l, or l/l).
Detailed Description
150 patients at University of Washington affiliated hospitals who are found to be depressed by DSMIV criteria within the first four months following ischemic stroke will be invited to join the study, and randomly assigned to a problem-solving/pleasant events intervention provided by an advanced practice nurse, or to regular clinic follow-up. Both groups will receive standard antidepressant treatment and written materials from the American Stroke Association, and will be assessed for up to two years following the study. The primary outcome is reduction in depression at 12 months following stroke. Secondary outcomes are reductions in limitations in activity (Barthel Index), reduction in limitation in participation (Stroke Impact Scale) and overall stroke impact (Stroke Impact Scale) at 6, 12, and 24 months post- stroke. We hypothesize that all patients will improve their mood and functional ability related to their post-stroke standard treatment, but that those who receive the psychosocial intervention will have significantly greater improvement in mood, functional ability, social participation, and less overall stroke impact at all follow-up measurement. A supplemental aim is to expand aim 4 of the parent study, adding SERT genotype to our list of factors that might influence treatment outcome for PSD. Further, since we are screening both depressed and not depressed stroke survivors for this study, we will add a fifth aim: to compare ischemic stroke survivors who are and are not depressed within the first four months following stroke by their 5-HTTLPR genotypes (s/s, s/l, or l/l).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
Keywords
Depressive symptoms, Behavior and behavior mechanisms, Recovery

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
101 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Nine session psychosocial/behavioral counseling with homework
Arm Title
2
Arm Type
Active Comparator
Arm Description
Usual clinic care with booklet describing depression following stroke
Intervention Type
Behavioral
Intervention Name(s)
Modified cognitive behavioral therapy plus problem-solving
Intervention Description
9 sessions with a psychosocial nurse practitioner in which participants learn to use behavioral strategies and specific problem-solving approaches to reduce or prevent behavioral and mood disturbances characteristic of stroke.
Intervention Type
Other
Intervention Name(s)
usual care
Intervention Description
Usual care with primary provider plus a booklet about mood and behavioral changes following stroke
Primary Outcome Measure Information:
Title
Reduction in depression (Hamilton Depression Rating Scale)at 12 months following stroke.
Time Frame
12 months following stroke
Secondary Outcome Measure Information:
Title
Reduction in limitations in activity (Barthel Index)6, 12, 24 months
Time Frame
6, 12, 24 months following intervention
Title
Reduction in limitation in participation (Stroke Impact Scale)6, 12, 24 months
Time Frame
6, 12, 24 months following intervention
Title
Overall stroke impact (Stroke Impact Scale)6,12,24 months post- stroke.
Time Frame
6, 12, 24 months following stroke

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Ischemic stroke within previous 4 months Screens positive for depressive symptoms by Geriatric Depression Scale Able to provide informed consent - Exclusion Criteria: Subarachnoid or intracranial hemorrhagic stroke Global aphasia Reduced level of consciousness (GCS <15)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pamela H Mitchell, PhD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Washington
City
Seattle
State/Province
Washington
ZIP/Postal Code
98195-7266
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
18436150
Citation
Mitchell PH, Teri L, Veith R, Buzaitis A, Tirschwell D, Becker K, Fruin M, Kohen R, Cain KC. Living well with stroke: design and methods for a randomized controlled trial of a psychosocial behavioral intervention for poststroke depression. J Stroke Cerebrovasc Dis. 2008 May-Jun;17(3):109-15. doi: 10.1016/j.jstrokecerebrovasdis.2007.12.002.
Results Reference
background
PubMed Identifier
21847802
Citation
Kohen R, Cain KC, Buzaitis A, Johnson V, Becker KJ, Teri L, Tirschwell DL, Veith RC, Mitchell PH. Response to psychosocial treatment in poststroke depression is associated with serotonin transporter polymorphisms. Stroke. 2011 Jul;42(7):2068-70. doi: 10.1161/strokeaha.110.611434.
Results Reference
derived
PubMed Identifier
19661478
Citation
Mitchell PH, Veith RC, Becker KJ, Buzaitis A, Cain KC, Fruin M, Tirschwell D, Teri L. Brief psychosocial-behavioral intervention with antidepressant reduces poststroke depression significantly more than usual care with antidepressant: living well with stroke: randomized, controlled trial. Stroke. 2009 Sep;40(9):3073-8. doi: 10.1161/STROKEAHA.109.549808. Epub 2009 Aug 6.
Results Reference
derived

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Psychosocial/Behavioral Intervention in Post-Stroke Depression

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