Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University
PRIMARY OBJECTIES:
I. To evaluate the feasibility of using the Carevive Survivor Care Planning System (SCPS) during the follow-up visit for breast oncology survivors treated in a university cancer center or a community medical center.
II. To evaluate survivors' perceptions of the usability of the Carevive technology.
III. To evaluate their perceptions of the acceptability (perception of benefit) of the treatment summary and survivor care plan.
SECONDARY OBJECTIVES:
I. Examine the psychometrics of surveys developed for this research. II. Compare participants' perceptions of the care received under the Carevive system with clinician documentation.
III. Compare clinician documentation of care received by this sample with documentation of care provided for historical controls at each site.
Age
18–any
Sex
FEMALE
Healthy volunteers
Not accepted
You may be eligible if
Prospective study: completed primary treatment for breast malignancies; receive survivorship care at Thomas Jefferson University (TJU) or Reading Health System (RHS)
Prospective study: individuals will have pathologically confirmed breast cancer (stages I-III)
Prospective study: Able to understand and read English
Prospective study: Physically capable of using a tablet computer (no severe visual, hearing, or hand motor deficits)
Retrospective chart review: Individuals will have pathologically confirmed breast cancer or gynecological (GYN) malignancies including uterine, ovarian, or cervical cancers, stages I-III; treated in the previous two years (2013-2014)
You may not be if
Women who are pregnant
Vulnerable populations: cognitively impaired; prisoners; terminally ill; elderly and infirm; drug addicts