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Study of Factors Influencing Post-stroke Dementia

Characterization of Clinical, Biological, Morphological and Pharmacological Factors Influencing Occurrence of Dementia or Cognitive Disorders After Stroke

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01330160
Acronym
strokdem
Enrollment
229
Registered
2011-04-06
Start date
2010-02-27
Completion date
2021-01-15
Last updated
2025-12-16

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

Conditions

Cerebrovascular Disorders, Dementia

Keywords

stroke, Brain ischemia, Intracranial hemorrhage, Dementia, Vascular, Alzheimer's disease

Brief summary

If the risk of dementia occurrence after stroke is well known, few data exist about the factors influencing positively or negatively the developement of cognitive disorders or dementia. The aim of the study is so to determine prospectively the clinical, biological, lesional and pharmacological factors associated with post-stroke dementia by the long-term follow-up of a stroke patient cohort.

Detailed description

The STROKDEM study is based on the 5-year prospective follow-up of a population of 1100 stroke patients without dementia. At inclusion in the cohort, main antecedents and risk factors, previous treatment and lifestyle, initial severity and etiology are recorded. Biological samples (for standard ans specialized analyses) and MRI are performed at 72h after stroke occurrence. Thereafter, patients are regularly (6 months, 12 months, 36 months, 60 months) examined for clinical and cognitive assessment with biological samples and Magnetic Resonance Imaging. Patients with dementia will be compared to patients without stroke to identify, by logistic regression analysis and Cox model, the factors associated with dementia occurrence.

Interventions

None listed

Sponsors

Ministry of Health, France
CollaboratorOTHER_GOV
University Hospital, Lille
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to 95 Years
Healthy volunteers
No

Inclusion criteria

* patients \> 40 years olds * hemispheric stroke * stroke dating from less 72h * IQ-code \< 64 * patient (or his family) given an informed consent

Exclusion criteria

* non hemispheric stroke * malformative intracranial hemorrhage * traumatic intracranial hemorrhage * subarachnoidal hemorrhage * contra-indication to MRI * patients unable to answer to cognitive battery

Design outcomes

Primary

MeasureTime frameDescription
dementia occurrence60 monthsThis evaluation will be based on a neurological and general clinical examination, and on the evaluation of activities of daily life using the Instrumental Activities Daily Life scale after an interview with the patient and his/her family.

Secondary

MeasureTime frameDescription
dementia occurrence and cognitive impairment6 monthsThis evaluation will be based on a neurological and general clinical examination, and on the evaluation of activities of daily life using the Instrumental Activities Daily Life scale after an interview with the patient and his/her family. Impairment of some tests of cognitive battery without significant impairment in activities of daily living
dementia occurence and cognitive impairment36 monthsThis evaluation will be based on a neurological and general clinical examination, and on the evaluation of activities of daily life using the Instrumental Activities Daily Life scale after an interview with the patient ans his/her family. Impairment of some tests of cognitive battery without significant impairment in activities of daily living
cognitive impairment36 monthsImpairment of some tests of cognitive battery without significant impairment in activities of daily living

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026