Clinical Trials Directory

Trials / Completed

CompletedNCT00071643

Preventing Post-Stroke Depression

Prevention of Post-Stroke Depression - Treatment Strategy

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
201 (actual)
Sponsor
Robert G. Robinson · Academic / Other
Sex
All
Age
31 Years – 89 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
BEHAVIORALProblem Solving TherapyProblem solving therapy aims to make patients aware of symptoms of problems and link those with behaviors associated with solving them.
DRUGEscitalopramParticipants will receive escitalopram, a selective serotonin reuptake inhibitor.
OTHERPlaceboParticipants will receive a placebo pill.

Timeline

Start date
2002-09-01
Primary completion
2008-11-01
Completion
2008-11-01
First posted
2003-10-30
Last updated
2017-09-05

Locations

3 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00071643. Inclusion in this directory is not an endorsement.