Clinical Trials Directory

Trials / Completed

CompletedNCT00262899

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

Genetic Counseling for Newly Diagnosed Breast Cancer Patients

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
331 (actual)
Sponsor
Georgetown University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed description

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.

Conditions

Interventions

TypeNameDescription
BEHAVIORALcounseling intervention
OTHEReducational intervention
PROCEDUREpsychosocial assessment and care

Timeline

Start date
2005-08-01
Primary completion
2010-07-01
Completion
2011-07-01
First posted
2005-12-07
Last updated
2013-01-07

Locations

4 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00262899. Inclusion in this directory is not an endorsement.