MedPath

Informing relatives about their cancer risk and preventive measures. A trial to assess the effectiveness of additional counseling.

Completed
Conditions
hereditary or familial breast cancer
hereditary or familial colon cancer
10083624
10017990
10006232
Registration Number
NL-OMON39133
Lead Sponsor
Academisch Medisch Centrum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
1200
Inclusion Criteria

Inclusion criteria for counselees:
1) index-patient (the first in their family to visit the department of Clinical Genetics for hereditary or familial colon or breast cancer),
2) at least one relative at increased risk for breast or colon cancer, i.e. eligible for genetic counseling and/or surveillance,
3) aged 18 years and over,
4) able to read and write Dutch and
5) informed consent. ;Inclusion criteria for relatives:
1) permission of the counselee,
2) aged 18 years and over,
3) able to read and write Dutch and
4) informed consent.

Exclusion Criteria

1) mentally impaired
2) unable to independently complete a questionnaire
3) they are not literate in Dutch

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The primary outcome constitutes the degree of knowledge, motivation and<br /><br>self-efficay of counselees with regard to disclosing cancer risks and<br /><br>preventive measures to relatives. </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>secondary outcomes include:<br /><br>- the number and proportion of relatives informed by counselees<br /><br>- relatives' knowledge about hereditary cancer and preventive measures<br /><br>- relatives' intention to engage in genetic counseling</p><br>
© Copyright 2025. All Rights Reserved by MedPath