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ATtention Test and Executive Functions After STroke to Predict Depression. (ATTEST-Depress)

C

Centre Hospitalier St Anne

Status

Completed

Conditions

Post-stroke Depression

Treatments

Other: Cognitive evaluation
Other: Evaluation of the psychiatric disorders
Other: Thymic history

Study type

Interventional

Funder types

Other

Identifiers

NCT04008719
D17-P02

Details and patient eligibility

About

The purpose of this study is to determine whether cognitive function evaluation (sustained attention, executive functions, working memory) during acute post-stroke is predictive of a 3 months post-stroke depression.

Full description

  1. Baseline visit: after neurologic stability, 14 days or less after stroke and before discharge.

  2. First assessment :

    1. Neurologic data: morphologic data (MRI of the brain), stroke severity (NIHSScore), aphasia assessment (Boston Diagnostic Aphasia Examination) if NIHS verbal score ≥1, hemineglect assessment (Bells test).
    2. Personal data assessment :

    i. Socio demographic : age, gender, marital status, employment, level of education ii. Medical history: medical treatments, psychiatric and non psychiatric history.

    c. Psychiatric assessment i. Mini International Neuropsychiatric Interview - depression ii. Beck Depression Inventory iii. Clinical Global Impression iv. Standardized Assessment of Personality - Abbreviated Scale (SAPAS) v. Fageström-C vi. Alcohol Use Disorders Identification Test (AUDIT-C) d. Cognitive assessment: i. Verbal memory : Dubois's five words ii. Clock drawing test iii. D2test (computerized) iv. Verbal fluency (Cardebat) v. Working memory (digit span WAIS 3) vi. Brixton (computerized)

  3. Assessment 3 months after the first assessment. Phone call and psychiatric assessment: MINI depression, Beck Depression Inventory. Barthel index and Quality of Life assessment.

Enrollment

74 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18 or more
  • Ischemic or hemorragic stroke, diagnosed with radiology : cerebral CT or MRI, 14 days or less after stroke
  • Signed Consent
  • Social insurance regime affiliation

Exclusion criteria

  • Death
  • No possibility of follow-up
  • No French-speaker : insufficient command of French
  • Deprivation of liberty : judicial or administrative decision
  • D2 test assessment impossibility
  • Aphasia with major disorder of the understanding (Boston <8)
  • Antidepressant treatment during stroke
  • Depression during stroke
  • protected people

Trial design

Primary purpose

Screening

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

74 participants in 1 patient group

Patients
Other group
Description:
Assessments are made by a psychiatrist
Treatment:
Other: Cognitive evaluation
Other: Thymic history
Other: Evaluation of the psychiatric disorders

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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