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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: Netherlands Trial Register
Last refreshed on: 28 April 2013
Main ID:  NTR1656
Date of registration: 03/02/2009
Primary sponsor: Erasmus Medical Center
Public title: Metamemory intervention in chronic stroke patients: long-term effects on social participation and quality of life.
Scientific title: Metamemory intervention in chronic stroke patients: long-term effects on social participation and quality of life. - Metamemory intervention in stroke
Date of first enrolment: 1/5/2008
Target sample size: 200
Recruitment status: recruiting
URL:  http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=1656
Study type:  intervention
Study design:  Randomised: Yes; Masking: Single; Control: Active; Group: Parallel; Type: 2 or more arms, randomized  
Countries of recruitment
The Netherlands
Contacts
Name: L.  Aben
Address:  Department of Rehabilitation medicine Erasmus University Medical Centre P.O. Box 2040 3000 CA Rotterdam The Netherlands
Telephone: +31 (0)10-2412412
Email: l.aben@erasmusmc.nl
Affiliation: 
Name: L.  Aben
Address:  Department of Rehabilitation medicine Erasmus University Medical Centre P.O. Box 2040 3000 CA Rotterdam The Netherlands
Telephone: +31 (0)10-2412412
Email: l.aben@erasmusmc.nl
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria: 1. First and only stroke;

2. A minimum of 18 months post onset;

3. Between 18 and 80 years of age;

4. Capable to handle additional burden of care;

5. Patients have to report memory complaints;

6. Independent living.

Exclusion criteria: 1. Progressive neurological disorders;

2. Insufficient understanding of the Dutch language;

3. Drug or alcohol abuse;

4. Subarachnoidal haemmorhage, subdural haematoma.


Age minimum:
Age maximum:
Gender:
Health Condition(s) or Problem(s) studied
Stroke

Intervention(s)
MSE-intervention versus peer-groups.
Primary Outcome(s)
The primary outcome measurements are level of memory self efficacy, level of quality of life and level of social participation.
Secondary Outcome(s)
Objective memory functioning and psychosocial factors like coping, depression and personality are measured.
Secondary ID(s)
NL21004.078.08
Source(s) of Monetary Support
KFA
Secondary Sponsor(s)
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