Health Status Unknown
Conditions
Brief summary
This pilot research trial studies how well questionnaires and cognitive assessments work in tracking patient symptoms following mammography. Gathering information over time through questionnaires and cognitive tests about symptoms patients may experience after a mammogram may help doctors understand the cause of these symptoms.
Detailed description
PRIMARY OBJECTIVES: I. To determine the feasibility of Internet-based cognitive assessments as preliminary data prior to larger clinical trial. OUTLINE: Patients complete questionnaires and cognitive assessments over 45-60 minutes within 3 weeks following mammography and at about 3 months in patients for whom biopsy is not required, before biopsy and at about 3 months in patients for whom biopsy is required, and at 4-6 weeks after first chemotherapy infusion in patients receiving chemotherapy.
Interventions
OTHERCognitive Assessment
Complete cognitive assessments
OTHERQuestionnaire Administration
Complete questionnaires
Sponsors
National Cancer Institute (NCI)
University of Southern California
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
FEMALE
Age
21 Years to 70 Years
Healthy volunteers
Yes
Inclusion criteria
* Mammography Breast Imaging Reporting and Data System (BI-RAD) 4-5; or BI-RAD 1-2 * Fluent in English * Access to Internet * Ability to understand and the willingness to sign a written informed consent
Exclusion criteria
* Prior abnormal mammography * Prior cancer diagnosis * Prior treatment with chemotherapy
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of patients invited who agree to participate | Up to 2 years | Number of patients invited will be reported. |
Countries
United States
Outcome results
None listed