Facilitating Web-based Patient Decision Support: Decision About Medication to Lower Breast Cancer Risk

Risk Reduction Behavior Clinical Trial

Official title:

Facilitating Web-Based Patient Decision Support: Decision About Medication to Lower Breast Cancer Risk

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00906321
• Other study ID #: 999909150
• Secondary ID: 09-C-N150
• Status: Completed
• Phase: N/A
• First received: May 20, 2009
• Last updated: June 30, 2017
• Start date: May 18, 2009
• Est. completion date: May 26, 2010

Study information

• Verified date: May 26, 2010
• Source: National Institutes of Health Clinical Center (CC)
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Background:

• Chemoprevention is the use of preventive medications to reduce the risk of breast cancer for women who are at a high risk of developing the disease. Although the treatment has shown effectiveness in preventing cancer development, chemoprevention is notably underutilized even by women who are at a high risk of developing breast cancer.

• Researchers are interested in determining if better decision support mechanisms, such as interactive Web sites, can help to overcome some of the barriers to chemoprevention.

Objectives:

• To develop and test a prototype Web-based module that will provide decision support to women who are considering chemoprevention for breast cancer.

Eligibility:

• Women 35 years of age and older who are at high risk for breast cancer and whose doctor has recommended chemoprevention (either Tamoxifen or Raloxifene), and who have no other history of cancer (apart from non-melanoma skin cancer or precancerous cervical lesions).

• Participants must have a working e-mail address and access to a computer with internet access and a telephone.

Design:

• Participants who are considering chemoprevention will be randomized to a Web-based decision support module or standard care online information resources.

• Participation lasts two months and involves using the online resources provided and filling out questionnaires two times during the study (at the beginning and the end).

The first time will be at the begin of the study.

• No medical treatments are offered as a part of this study

Description:

BACKGROUND:

• Breast cancer chemoprevention has been notably underutilized.

• Barriers to integrating breast cancer risk reducing measures include: lack of time, low priority of risk reduction in comparison to treatment, the need to personalize risks and benefits of chemoprevention, and the need for resources/information necessary for women to make informed decisions.

• Access to quality decision support resources to facilitate making informed, preference-sensitive decisions about chemoprevention may provide a mechanism to overcome some of the current barriers to chemoprevention utilization.

OBJECTIVES:

• Develop and refine a web-based patient decision support module for high-risk women making a decision about breast cancer chemoprevention.

• Conduct a randomized study of TACHD decision support versus standard care online information support to evaluate the impact of the chemoprevention module of the TACHD decision support intervention.

ELIGIBILITY:

• Women with no history of cancer other than cervical carcinoma in situ or non-melanoma skin cancer

• High risk for breast cancer based on at least one of the following:

• Gail score > 1.67

• History of atypical hyperplasia (either ductal or lobular)

• History of lobular carcinoma in situ

• Documentation of a deleterious BRCA1 or BRCA2 mutation

• Considering a decision about chemoprevention with tamoxifen or raloxifene

• Access to an IBM-compatible or MacIntosh personal computer with broadband Internet access

• Access to an email account

• Access to a telephone

• Aged 35 or older

• Able to communicate in English verbally and in writing

DESIGN:

• The project will be guided by the Cognitive-Social Health Information Processing (CSHIP) model overall, and incorporate the Ottawa Decision Support. Framework (ODSF) in one consistent decision support process.

• Testing of the chemoprevention decision support module will be conducted in a two-group pre- post-test experimental design with 64 at-risk women identified through Fox Chase Risk Assessment Programs and the NCI Clinical Cancer Genetics Program (CCGP) at the National Naval Medical Center (NNMC).

• A process evaluation analysis will assess participants' experiences using TACHD.

Other known NCT identifiers

• NCT00953238

Recruitment information / eligibility

• Status: Completed
• Enrollment: 64
• Est. completion date: May 26, 2010
• Est. primary completion date: May 26, 2010
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 35 Years to 100 Years

Eligibility

-INCLUSION CRITERIA:

1. Women with no history of cancer other than cervical carcinoma in situ or non-melanoma skin cancer

2. High risk for breast cancer based on at least one of the following:

• Gail score > 1.67

• History of atypical hyperplasia (either ductal or lobular)

• History of lobular carcinoma in situ

• Documentation of a deleterious BRCA1 or BRCA2 mutation

3. Considering a decision about chemoprevention with tamoxifen or raloxifene

4. Access to an IBM-compatible or MacIntosh personal computer with broadband Internet access

5. Access to an email account

6. Access to a telephone

7. Aged 35 or older

8. Able to communicate in English verbally and in writing

9. Women of all races and ethnic groups are eligible for this study.

EXCLUSION CRITERIA:

1. Concurrent participation in another cancer chemoprevention study

2. Prior history of cancer, other than cervical carcinoma in situ or non-melanoma skin cancer

3. Ever taken tamoxifen or raloxifene

4. Age less than 35

5. Unable to communicate in English verbally and in writing

6. No computer with internet access

7. No email account

8. No telephone

Related Conditions & MeSH terms

• Breast Neoplasms
• High Risk for Breast Cancer
• Risk Reduction Behavior

Intervention

Behavioral:
• Web-Based Decision Support

Locations

Country	Name	City	State
United States	National Cancer Institute (NCI), 9000 Rockville Pike	Bethesda	Maryland

Sponsors (1)

Lead Sponsor	Collaborator
National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

References & Publications (3)

Collins FS. Shattuck lecture--medical and societal consequences of the Human Genome Project. N Engl J Med. 1999 Jul 1;341(1):28-37. — View Citation

Guttmacher AE, Collins FS. Genomic medicine--a primer. N Engl J Med. 2002 Nov 7;347(19):1512-20. Review. — View Citation

Rose AL, Peters N, Shea JA, Armstrong K. Attitudes and misconceptions about predictive genetic testing for cancer risk. Community Genet. 2005;8(3):145-51. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Conduct a formative evaluation of the impact of the chemoprevention module of the Trusted Advisor for Cancer Health Decisions (TACHD) decision support intervention