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Clinical Trials/NCT00071643
NCT00071643
Completed
Not Applicable

Prevention of Post-Stroke Depression - Treatment Strategy

Robert G. Robinson3 sites in 1 country201 target enrollmentSeptember 2002

Overview

Phase
Not Applicable
Intervention
Problem Solving Therapy
Conditions
Depression
Sponsor
Robert G. Robinson
Enrollment
201
Locations
3
Primary Endpoint
Incidence of depressive disorders in the study population
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

This study will evaluate the effectiveness of both drug and non-drug treatments in preventing depression after a stroke.

Detailed Description

The development of depression after a stroke is a serious condition that can have negative effects on thought, emotions, and overall daily functioning, particularly in the first year following the stroke. Evidence suggests that antidepressants may be used to prevent post-stroke depression. This study will treat nondepressed stroke patients with antidepressants or problem solving therapy (PST) to determine the most effective treatments for preventing depression. Participants in this study will be randomly assigned to receive PST, escitalopram, or placebo (an inactive pill) for 12 months. Participants who display depressive symptoms for 2 weeks or more will be removed from the study. After 12 months, treatment will be discontinued and participants will be monitored for an additional 6 months.

Registry
clinicaltrials.gov
Start Date
September 2002
End Date
November 2008
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Robert G. Robinson
Responsible Party
Sponsor Investigator
Principal Investigator

Robert G. Robinson

Professor

University of Iowa

Eligibility Criteria

Inclusion Criteria

  • Stroke within the last 120 days

Exclusion Criteria

  • DSM (Diagnostic and Statistical Manual) IV criteria for major or minor depressive disorder
  • Heart, respiratory, kidney, or liver failure; severely disabling musculoskeletal disorder; or cancer
  • Diagnosis of neurodegenerative disorders such as Parkinson's disease, Alzheimer's disease, Multiple System Atrophy, or Huntington's disease
  • Pre-existing dementia or aphasia with severe language comprehension deficits
  • Alcohol or substance abuse or dependence within the last 12 months
  • Recurrent unipolar or bipolar disorder prior to the stroke

Arms & Interventions

1 Problem Solving Therapy

Participants will receive problem solving therapy.

Intervention: Problem Solving Therapy

2. Escitalopram

Participants will receive escitalopram.

Intervention: Escitalopram

3 Placebo

Participants will receive placebo.

Intervention: Placebo

Outcomes

Primary Outcomes

Incidence of depressive disorders in the study population

Time Frame: Measured at baseline, Week 6, and Months 3, 6, 9, 12, and 18

Secondary Outcomes

  • Functional Independence Measure(Measured at baseline, at Week 6, and at Months 3, 6, 9, 12, and 18)
  • Stroke Impact Scale(Measured at baseline, Week 6, and Months 3, 6, 9, 12, and 18)
  • Neurocognitive tests of executive functions and speed of information processing(Measured at baseline and after 12 months)

Study Sites (3)

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