NCT Number: NCT00262899
Genetic Counseling or Usual Care in Helping Women With Newly Diagnosed Ductal Carcinoma In Situ or Stage I, Stage II, or Stage IIIA Breast Cancer Make Treatment Decisions
RATIONALE: Genetics education and counseling may help patients make treatment decisions. It is not yet known how genetic counseling or usual care influence patient treatment decisions for breast cancer.
PURPOSE: This randomized clinical trial is studying how well genetic counseling works compared to usual care in helping patients with newly diagnosed ductal carcinoma in situ, stage I, stage II, or stage IIIA breast cancer make treatment decisions.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
Female
Study type
Interventional
Phase
Phase 3
Primary location
Lombardi Comprehensive Cancer Center at Georgetown University Medical Center, Washington D.C., District of Columbia, United States
About this study
OBJECTIVES:
- Compare the impact of rapid genetic counseling (RGC) vs usual care on the medical decisions of women with newly diagnosed ductal carcinoma in situ or stage I-IIIA breast cancer.
- Compare the impact of these interventions on the quality of life and psychological well being of these patients.
- Determine baseline factors that predict who is most and least likely to benefit from RGC in patients undergoing these interventions.
- Compare the cost per quality adjusted life year saved from a societal perspective in patients undergoing these interventions.
OUTLINE: This is a randomized, multicenter study. Patients are stratified according to participating site. Patients are randomized to 1 of 2 interventional arms.
- Arm I (rapid genetic counseling): Patients undergo a 1½ hour genetic counseling session either in person or by telephone. Patients who undergo telephone counseling receive a booklet of visual aids and educational materials. Patient preferences and values are assessed immediately after counseling. Some patients may undergo BRCA1/2 status determination. Patients undergo follow-up telephone interviews at 1, 6, and 12 months.
- Arm II (usual care): Patients receive a packet of breast cancer treatment educational materials. Patient preferences and values are assessed 2 weeks later. Patients undergo follow-up telephone interviews as in arm I.
In both arms, quality of life is assessed at baseline and at 1, 6, and 12 months.
After completion of the study, patients are followed periodically for 1 year.
PROJECTED ACCRUAL: A total of 360 patients will be accrued for this study.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
DISEASE CHARACTERISTICS:
- Newly diagnosed breast cancer, meeting 1 of the following criteria:
- Stage 0 disease (ductal carcinoma in situ only)
- Stage I-IIIA disease
- Must meet 1 of the following criteria:
- Diagnosis before 50 years of age
- Diagnosis after 50 years of age AND has 1 of the following:
- First or second degree relative diagnosed with breast cancer before 50 years of age
- First or second degree relative diagnosed with ovarian cancer at any age
- First or second degree relative diagnosed with male breast cancer at any age
- Must not have initiated definitive treatment for breast cancer
- No bilateral, metastatic, or inflammatory breast cancer
- No prior BRCA1/2 counseling or testing
- No prior diagnosis of metastatic cancer of any type
- Hormone receptor status:
- Not specified
PATIENT CHARACTERISTICS:
Sex
- Female
Menopausal status
- Not specified
Performance status
- Not specified
Life expectancy
- Not specified
Hematopoietic
- Not specified
Hepatic
- Not specified
Renal
- Not specified
PRIOR CONCURRENT THERAPY:
Surgery
- No prior bilateral mastectomy for breast cancer
Other
- No concurrent treatment for cancer
Treatment and study plan
Educational Intervention
Otherpsychosocial assessment and care
ProcedurePrimary outcomes
-
Definitive surgery choice as measured by self-reported and medical record verification at 6 months after randomization
Time frame: 1, 6, and 12 months
-
Quality of life as measured by functional assessment of cancer therapy for breast cancer (FACT-B) at 1, 6, and 12 months after randomization
Time frame: 1, 6, and 12 months
-
Distress as measured by Impact of Events Scale Brief Symptom Inventory at 1, 6, and 12 months after randomization
Time frame: 1, 6, and 12 months
-
Knowledge as assessed by Genetic Testing Knowledge Measure at 1 month after randomization
Time frame: 1 month
-
Decision outcomes as assessed by Decisional Conflict Scale Satisfaction with Decision Scale at 1 and 6 months after randomization
Time frame: 1 and 6 months
Secondary outcomes
-
Cost effectiveness as measured by quality adjusted life years saved at 12 months after randomization
Time frame: 12 months
Sponsors and collaborators
Lead sponsor
Georgetown University
Other
Collaborators
- National Cancer Institute (NCI)
Registry information
Official study title
Genetic Counseling for Newly Diagnosed Breast Cancer Patients
Important dates
- Study start
- 2005
- Primary completion
- 2010
- Study completion
- 2011
- First posted
- Dec 7, 2005
- Registry last updated
- Jan 7, 2013
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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