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Post-stroke Depression Treatment Effect on Stroke Recurrence

Impact of Pots-stroke Depression Treatment on Stroke Recurrence

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04776226
Acronym
STROKE
Enrollment
1230
Registered
2021-03-01
Start date
2017-02-11
Completion date
2019-03-30
Last updated
2021-03-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Events, Depression, Stroke Recurrence

Keywords

Depression, Treatment, Stroke, Myocardial infarction

Brief summary

It is not clear whether depresssion can predispose, or precipitate stroke recurrence in patients with stroke. We sought the relationship of post stroke depression with stroke recurrence.

Detailed description

A large body of evidence suggests that depression is associated with a increased risk of many chronic diseases, including hypertension, diabetes, stroke and particularly coronary heart disease. Post stroke depression (PSD) may develop as a result of vascular disease. A previous meta-analysis showed that depression significantly increased the risk of development of stroke, and this increase was probably independent of other risk factors, including hypertension and diabetes. Clarifying this issue has important implications; if depression increases the risk of development of recurrent stroke, so treating PSD might decrease the occurrence of recurrent stroke. To our knowledge there is no study attempting to clarify the relationship between PSD treatment and stroke recurrence. To fill these gap, we systematically conducted a study to assess whether PSD is associated with recurrent stroke, cardiovascular events or death. Thus, in the current study, three different arms of follow-up of patients with first-ever stroke, were used to predict the outcome over 52 weeks.

Interventions

DRUGCitalopram

Antidepressant use in patients with depression

Sponsors

Ege University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

There is no masking

Intervention model description

Three-site, prospective, nonrandomized controlled trial.

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

• Patients who met DSM-IV and V criteria for depression

Exclusion criteria

* Severe or unstable medical disorders (eg, myocardial infarction within past 3 months, end-stage cancer, decompensated cardiac failure) * Known primary neurological disorders including dementia, delirium, Parkinson disease, brain tumors, multiple sclerosis, seizure disorder * Drugs (eg, systemic steroids) * Pancreatic cancer, uncorrected hypothyroidism * Current suicidal risk * Use of psychotropic prescription or nonprescription drugs, certain hypnotics * Mini-Mental State Examination (MMSE) score of 21 or lower

Design outcomes

Primary

MeasureTime frameDescription
Stroke recurrence12 monthsStandard World Health Organization definitions were used for recurrent stroke

Secondary

MeasureTime frameDescription
Cardiovascular Event12 monthsCardiovascular events were defined and recorded over the study period if they had at least one of the following: myocardial infarction; unstable angina; angina; percutaneous coronary intervention; or coronary artery bypass graft surgery.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026