Breast Cancer
Conditions
Keywords
Diagnostic Imaging, Breast Screening, Breast Cancer, To be eligible for the study, subjects must:, Be females at least 18 years of age,, Have had their screening mammogram performed at the UW Breast Center,, Be able to read and write English at the 6th grade level (as shown by their, ability to understand the informed consent),, Have access to a computer with internet capability.
Brief summary
This project evaluates the impact of CHESS-Mammo by assessing participants' health information competence, psychological distress, and satisfaction with their doctor as measured by previously validated survey questionnaires.
Detailed description
The study consists of two parts. Part 1 (focus groups) interviewed 11 women in total (6 diagnosed with breast cancer and 5 diagnosed with benign breast disease) reinforced the need for online information during the breast diagnostic process. The focus group reviewed online CHESS-Mammo module and suggested minor changes to content. Part 2 (Evaluation) will enroll 130 women in study and compare one group (65 participants) who receives access to CHESS-Mammo to another group of women (65 participants) who receive an email message containing screening mammography information. Both groups in Part 2 will be evaluated for health information competence, psychological distress, and patient satisfaction with physician through questionnaires. An evaluation of the group that accesses the CHESS-Mammo website will be done. The reason for conducting part 2 of this study is to allow greater insight into the clinical application of a novel Interactive Cancer Communication Systems (CHESS-Mammo) early in the diagnostic workup of breast cancer. By doing this project, we may achieve an important new way of implementing CHESS-Mammo in the clinic.
Interventions
BEHAVIORALComprehensive Health Enhancement Support System (CHESS.)
Half of the participating women will be randomly assigned to usual care and half will be offered a fully CHESS.
Sponsors
National Cancer Institute (NCI)
University of Wisconsin, Madison
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
To be eligible for the study, subjects must: * Be females at least 18 years of age, * Have had their screening mammogram performed at the UW Breast Center, * Be able to read and write English at the 6th grade level (as shown by their, ability to understand the informed consent), * Have access to a computer with internet capability.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| This design will allow us to compare the health information competence, psychological distress, and patient satisfaction with their doctor among the two groups. | 3 weeks | This is a randomized controlled trial in which half of the participants will receive access to CHESS-Mammo during their diagnostic workup of an abnormal screening mammogram, and the other half will receive basic information in addition to usual care. This design will allow us to compare the health information competence, psychological distress, and patient satisfaction with their doctor among the two groups. |
Countries
United States
Outcome results
None listed