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Main
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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. |
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Register:
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Netherlands Trial Register |
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Last refreshed on:
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28 April 2013 |
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Main ID: |
NTR1656 |
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Date of registration:
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03/02/2009 |
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Primary sponsor: |
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Public title:
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Metamemory intervention in chronic stroke patients: long-term effects on social participation and quality of
life.
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Scientific title:
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Metamemory intervention in chronic stroke patients: long-term effects on social participation and quality of
life. - Metamemory intervention in stroke |
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Date of first enrolment:
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1/5/2008 |
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Target sample size:
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200 |
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Recruitment status: |
recruiting |
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URL:
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http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=1656 |
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Study type:
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intervention |
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Study design:
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Randomised: Yes; Masking: Single; Control: Active; Group: Parallel; Type: 2 or more arms, randomized
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Countries of recruitment
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The Netherlands
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Contacts
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Name:
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L.
Aben |
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Address:
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Department of Rehabilitation medicine
Erasmus University Medical Centre
P.O. Box 2040
3000 CA
Rotterdam
The Netherlands |
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Telephone:
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+31 (0)10-2412412 |
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Email:
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l.aben@erasmusmc.nl |
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Affiliation:
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Name:
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L.
Aben |
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Address:
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Department of Rehabilitation medicine
Erasmus University Medical Centre
P.O. Box 2040
3000 CA
Rotterdam
The Netherlands |
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Telephone:
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+31 (0)10-2412412 |
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Email:
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l.aben@erasmusmc.nl |
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Affiliation:
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Key inclusion & exclusion criteria
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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:
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Health Condition(s) or Problem(s) studied
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Stroke
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Intervention(s)
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MSE-intervention versus peer-groups.
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Primary Outcome(s)
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The primary outcome measurements are level of memory self efficacy, level of quality of life and level of social participation.
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Secondary Outcome(s)
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Objective memory functioning and psychosocial factors like coping, depression and personality are measured.
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Secondary ID(s)
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NL21004.078.08
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Source(s) of Monetary Support
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KFA
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