Cognitive and Emotional Impairment After Stroke

• Register: ClinicalTrials.gov
• Last refreshed on: 17 October 2012
• Main ID: NCT00506818
• Date of registration: 23/07/2007
• Primary sponsor: Sykehuset Asker og Baerum
• Public title: Cognitive and Emotional Impairment After Stroke
• Scientific title: Cognitive and Emotional Impairment After Stroke
• Date of first enrolment: February 2007
• Target sample size: 250
• Recruitment status: Completed
• URL: http://clinicaltrials.gov/show/NCT00506818
• Study type: Interventional
• Study design: Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Prevention

Countries of recruitment

Norway

Contacts

• Name: Hege Ihle-Hansen, MD
• Affiliation: Sykehuset Asker og Baerum

Key inclusion & exclusion criteria

Inclusion Criteria:

- First ever stroke or TIA

- No cognitive decline (IQCODE < 3,7)

- Survived the acute stroke

- Expected to live at least for one year after stroke

Exclusion Criteria:

- Cognitive decline



Age minimum: N/A
Age maximum: N/A
Gender: Both

Health Condition(s) or Problem(s) studied

Cognitive Impairment

Stroke

Vascular Dementia

Intervention(s)

Other: Multifactorial vascular-risk-factor-intervention

Primary Outcome(s)

Effects of vascular risk-factor-intervention on changes in TMTA, ten-words-test and HAD [Time Frame: 8-12 months after stroke onset]

Secondary Outcome(s)

Prevalence of dementia and depression after stroke [Time Frame: 8-12 month after stroke onset]

Secondary ID(s)

1.2006.2076(REK)

16307(NSD)

Source(s) of Monetary Support

Please refer to primary and secondary sponsors

Secondary Sponsor(s)

University of Oslo