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Spots Global Cancer Trial Database for Cancer Prevention in Women With a BRCA Mutation

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Cancer Prevention in Women With a BRCA Mutation

Official Title: Cancer Prevention in Women With a BRCA Mutation: A Follow-up Genetic Counselling Intervention

Study ID: NCT02225015

Study Description

Brief Summary: This study aims to develop a follow-up telephone-based genetic counselling (FTGC) intervention for women with a BRCA1 or BRCA2 mutation who have received genetic counseling in the past. Typically, when women undergo genetic testing, they receive standard genetic counselling prior to testing in order to fully understand the procedure and associated implications. If a woman's genetic test results are positive for a mutation, cancer prevention options are then discussed with a counsellor. However, in Canada, there is currently no formal follow-up counselling for women with a BRCA mutation to provide ongoing guidance and support about latest risk reduction strategies. Standard care relies on women making contact for any follow-up questions or concerns they may have. As a result, these women might not have the most current information regarding genetic risk assessment and prevention options. Therefore, individuals are being asked to participate in this study to aid research about the efficacy of FTGC in women with a BRCA mutation.

Detailed Description:

Eligibility

Minimum Age: 35 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

London Regional Cancer Centre, London, Ontario, Canada

Women's College Hospital, Toronto, Ontario, Canada

Princess Margaret Hospital, Toronto, Ontario, Canada

Contact Details

Name: Kelly Metcalfe, Dr.

Affiliation: University of Toronto

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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