Carevive Survivor Care Planning System in Improving Quality of Life in Breast Cancer Survivors
| Status: | Completed |
|---|---|
| Conditions: | Breast Cancer, Ovarian Cancer, Cervical Cancer, Cervical Cancer, Cervical Cancer, Cervical Cancer, Cervical Cancer, Cervical Cancer, Cervical Cancer, Cervical Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Women's Studies |
| Therapuetic Areas: | Oncology, Reproductive |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 2/23/2018 |
| Start Date: | August 1, 2015 |
| End Date: | October 31, 2016 |
A Pilot Study of the Clinical Implementation of the Carevive Survivor Care Planning System
This pilot clinical trial studies how well the Carevive Survivor Care Planning System works
in improving quality of life in breast cancer survivors. A personalized survivor care plan
includes a summary of a patient's cancer treatment and a customized survivor care plan and
may provide beneficial information and resources.
in improving quality of life in breast cancer survivors. A personalized survivor care plan
includes a summary of a patient's cancer treatment and a customized survivor care plan and
may provide beneficial information and resources.
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.
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.
Inclusion Criteria:
- 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)
Exclusion Criteria:
- Women who are pregnant
- Vulnerable populations: cognitively impaired; prisoners; terminally ill; elderly and
infirm; drug addicts
We found this trial at
2
sites
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