Improving informed consent to clinical trials: Evaluating a decision aid for women invited to participate in a breast cancer prevention trial (IBIS-II).
Completed
- Conditions
- evel of informed consent in women considering joining IBIS-II (i.e. women with DCIS and at elevated risk of breast cancer).Level of informed consent in women considering joining IBIS-II (i.e. women with DCIS and at elevated risk of breast cancer).Cancer - Breast
- Registration Number
- ACTRN12605000506695
- Lead Sponsor
- Medical Psychology Research Unit, University of Sydney
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 400
Inclusion Criteria
Patients who are eligible for the IBIS-II trial will be eligible for the decision aid trial. These are either women at elevated risk of breast cancer, or women who have been treated for DCIS, aged between 40 and 70 years.
Exclusion Criteria
Insufficient English to read the booklet and complete questionnaires.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method