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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: |
NTR887 |
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Date of registration:
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18/01/2007 |
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Primary sponsor: |
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Public title:
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RCT in breast cancer genetic counselling.
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Scientific title:
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Web-based tailored information and question prompt for enhancing counselee participation and outcome; a RCT in breast cancer genetic counselling. - RCT in breast cancer genetic counselling |
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Date of first enrolment:
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1/9/2007 |
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Target sample size:
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200 |
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Recruitment status: |
complete |
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URL:
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http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=887 |
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Study type:
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intervention |
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Study design:
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Randomised: Yes; Masking: None; 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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A.
Albada |
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Address:
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NIVEL (Neterlands Institute for Health Services Research)
Postbus 1568, Otterstraat 118-124
3500 BN
Utrecht
The Netherlands |
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Telephone:
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(+31) (0)30 272 97 00 |
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Email:
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a.albada@nivel.nl |
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Affiliation:
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Name:
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S.
Dulmen, van |
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Address:
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NIVEL (Neterlands Institute for Health Services Research)
Postbus 1568, Otterstraat 118-124
3500 BN
Utrecht
The Netherlands |
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Telephone:
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(+31) (0)30 272 97 00 |
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Email:
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s.vandulmen@nivel.nl |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion criteria: 1.Counselee for breast cancer genetic counselling;
2. Age 18 or older;
3. Female gender;
4. Having internet access at home.
Exclusion criteria: 1. Age under 18;
2. Male gender;
3. Not having internet access at home.
Age minimum:
Age maximum:
Gender:
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Health Condition(s) or Problem(s) studied
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Breast cancer, Genetic counseling, Web-based tailored , Communication
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Intervention(s)
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The information on the website (E-info geneca) is tailored to counselees' personal situation as guided by their answers on our previously developed 'QUOTE geneca' scale. This produces different packages of pre-visit information in content, extensiveness and complexity and may generate a variety of questions to be dealt with in the subsequent visit. E-info geneca will be developed by a multi-disciplinary team of genetic counsellors, psychologists, counselees and their relatives and using recent brochures of the Dutch Cancer Society.
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Primary Outcome(s)
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Counselees' participation, i.e. content and amount of questions asked and information received during the visit.
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Secondary Outcome(s)
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1. Realistic expectations;
2. Information recall;
3. Need fulfilment;
4. Satisfaction;
5. Pre-post changes in breast cancer knowledge;
6. Risk perception;
7. Personal control;
8. Cancer worry;
9. (Intended) adherence to screening advices or prophylactic surgery at 12 months;
10. Satisfaction with e-info gene;
11. Anxiety.
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Secondary ID(s)
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ISRCTN82643064
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N/A
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Source(s) of Monetary Support
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Dutch Cancer Society
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