Trials / Completed

CompletedNCT03198286

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

A Pilot Study of the Clinical Implementation of the Carevive Survivor Care Planning System

Status: Completed
Phase: N/A
Study type: Interventional
Enrollment: 40 (actual)

Sponsor: Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University · Academic / Other
Sex: Female
Age: 18 Years
Healthy volunteers: Not accepted

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.

Detailed 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.

Conditions

Interventions

Type	Name	Description
OTHER	Informational Intervention	Receive treatment summary and survivor care plan

Timeline

Start date: 2015-08-01
Primary completion: 2015-08-01
Completion: 2016-10-31
First posted: 2017-06-26
Last updated: 2025-04-29

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT03198286. Inclusion in this directory is not an endorsement.