Carevive Survivor Care Planning System in Improving Quality of Life in Breast Cancer Survivors

Last updated: April 28, 2025
Sponsor: Sidney Kimmel Cancer Center at Thomas Jefferson University
Overall Status: Completed

Phase

N/A

Condition

Uterine Fibroids

Ovarian Cysts

Cervical Cancer

Treatment

Informational Intervention

Clinical Study ID

NCT03198286
15P.046
JT 7206
  • Ages > 18
  • Female

Study Summary

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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Prospective study: completed primary treatment for breast malignancies; receivesurvivorship 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 breastcancer or gynecological (GYN) malignancies including uterine, ovarian, or cervicalcancers, stages I-III; treated in the previous two years (2013-2014)

Exclusion

Exclusion Criteria:

  • Women who are pregnant

  • Vulnerable populations: cognitively impaired; prisoners; terminally ill; elderly andinfirm; drug addicts

Study Design

Total Participants: 40
Treatment Group(s): 1
Primary Treatment: Informational Intervention
Phase:
Study Start date:
August 01, 2015
Estimated Completion Date:
October 31, 2016

Study Description

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.

Connect with a study center

  • Sidney Kimmel Cancer Center at Thomas Jefferson University

    Philadelphia, Pennsylvania 19107
    United States

    Site Not Available

  • Reading Hospital

    Reading, Pennsylvania 19602
    United States

    Site Not Available

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