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CompletedNCT00588705Updated Jan 30, 2017

The Communication of Genetic Risk to Adolescent Daughters of Women With Breast Cancer

An observational study in Breast Cancer and Counseling, sponsored by Memorial Sloan Kettering Cancer Center. Completed at 1 site in United States. Open to female participants aged 12 Years to 20 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-01-30.

Sponsored by Memorial Sloan Kettering Cancer Center · Observational

Study type
Observational
Model
Family-based
Time perspective
Prospective
Enrollment
27
Ages
12 Years to 20 Years
Sex
Female
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Study summary

The purpose of this study is to first understand how MSKCC Clinical Genetics Service doctors talk to women with breast cancer about any genetic risks they might carry, and if they help women to think about what they might say, in turn, to their relatives, especially their daughters.

A second part of the study asks women for their opinions about when and how their daughters should be told about any genetic risks.

All of this will help us develop teaching methods to help our doctors improve the way they talk about genetic risk when women with breast cancer have adolescent daughters.

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Conditions studied

  • Breast Cancer
  • Counseling

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Keywords

  • Daughters
  • Communication
  • genetic risk
  • Genetic Counseling
03

In context

Breast Neoplasms

12,544 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.

This study's enrollment of 27 is below the median of 184 across 2,642 observational studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Memorial Sloan Kettering Cancer Center is the lead sponsor of 1,930 studies on the registry; 328 are open to participants now.

Of its 129 completed or terminated interventional studies of FDA-regulated products, 66 (51%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
12 Years to 20 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Memorial Sloan-Kettering Cancer Center (MSK) breast cancer patients seen by the clinical genetics service (CGS)and their daughters

Inclusion criteria

  • Women seen in the MSK CGS Service who have a diagnosis of breast cancer or
  • a family history of breast cancer and
  • have biological daughter(s) in the age range 12-20 years will be eligible to participate in Phase I \& II.
  • Women who were consented to Phase I will automatically be eligible for Phase II.

Exclusion criteria

Exclusion Criteria:

  • Women seen in the MSK CGS Service will be ineligible if they have no diagnosis of breast cancer and no family history of breast cancer,
  • do not have a biological daughter,
  • or have a biological daughter fewer than 12 or greater than 20 years(unless they were consented to Phase 1).
  • Women will be ineligible if they are not English speaking,
  • have intellectual or cognitive impairment,
  • or active mental illness rendering them incapable of giving informed consent, such as might occur with active psychosis.
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Study design

Observational model
Family-based
Time perspective
Prospective
Enrollment
27 participants (actual)

Groups and cohorts

  • focus group & questionaire

    The group will discuss its views about how and when to talk about the risk of getting breast cancer. The focus group will be video recorded and the video recorded material will be later transcribed and carefully analyzed. In addition you will be asked to answer questions about yourself, such as education and marital status.

    Behavioral: focus group & questionaire

Interventions

  • Behavioralfocus group & questionaire

    The focus group will last about 90 minutes. However, your involvement in this study will last from the time you join until you read over the summary of what happened during the focus group and return your comments. This should be approximately 2 months. Patient will complete a questionnaire and we estimate total time for completion to be approximately 7 minutes.

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What researchers measure

Primary outcomes

  1. Is a demonstration of the effectiveness of the module in changing the behavior of clinicians after taking part in the communication skills module.

    Time frame: conclusion of study

Secondary outcomes

  1. To examine the views of women about the provision of genetic risk information to their daughters.

    Time frame: conclusion of study

07

Study locations

1 site
  • Memorial Sloan-Kettering Cancer Center
    New York, New York 10065, United States
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References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 30, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00588705
Lead sponsor
Memorial Sloan Kettering Cancer Center
Collaborators
Monash University
Responsible party
Sponsor
First posted
Jan 8, 2008
Start date
Dec 2007
Primary completion
Jan 2017
Completion
Jan 2017
Last update
Jan 30, 2017

Study contacts

Smita Banerjee, PhD
principal investigator · Memorial Sloan Kettering Cancer Center
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2017. You cannot join it, but the record below documents what was studied.

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