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

NCT03198286 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2025-04-29

No results posted yet for this 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.

Conditions

  • Stage I Breast Cancer
  • Stage I Cervical Cancer
  • Stage I Ovarian Cancer
  • Stage I Uterine Corpus Cancer
  • Stage IA Breast Cancer
  • Stage IA Cervical Cancer
  • Stage IA Ovarian Cancer
  • Stage IA Uterine Corpus Cancer
  • Stage IB Breast Cancer
  • Stage IB Cervical Cancer
  • Stage IB Ovarian Cancer
  • Stage IB Uterine Corpus Cancer
  • Stage IC Ovarian Cancer
  • Stage II Breast Cancer
  • Stage II Cervical Cancer
  • Stage II Ovarian Cancer
  • Stage II Uterine Corpus Cancer
  • Stage IIA Breast Cancer
  • Stage IIA Cervical Cancer
  • Stage IIA Ovarian Cancer
  • Stage IIB Breast Cancer
  • Stage IIB Cervical Cancer
  • Stage IIB Ovarian Cancer
  • Stage IIC Ovarian Cancer
  • Stage III Breast Cancer
  • Stage III Cervical Cancer
  • Stage III Ovarian Cancer
  • Stage III Uterine Corpus Cancer
  • Stage IIIA Breast Cancer
  • Stage IIIA Cervical Cancer
  • Stage IIIA Ovarian Cancer
  • Stage IIIA Uterine Corpus Cancer
  • Stage IIIB Breast Cancer
  • Stage IIIB Cervical Cancer
  • Stage IIIB Ovarian Cancer
  • Stage IIIB Uterine Corpus Cancer
  • Stage IIIC Breast Cancer
  • Stage IIIC Ovarian Cancer
  • Stage IIIC Uterine Corpus Cancer

Interventions

OTHER

Informational Intervention

Receive treatment summary and survivor care plan

Sponsors & Collaborators

  • Sidney Kimmel Cancer Center at Thomas Jefferson University

    lead OTHER

Principal Investigators

  • Andrea Barsevick, PhD · Sidney Kimmel Cancer Center at Thomas Jefferson University

Study Design

Allocation
NA
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-08-01
Primary Completion
2015-08-01
Completion
2016-10-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03198286 on ClinicalTrials.gov