N/A
Completed N=66
The ConnectedCancerCare Pilot Study (CCC)
Early-Stage Breast Cancer · Breast Cancer Female · Survivorship · Cancer Survivors
Source: ClinicalTrials.gov NCT03618017 ↗
Enrolled (actual)
66
Serious AEs
0.0%
Results posted
Nov 2020
Primary outcomePrimary: Number of Breast Cancer Patients Successfully Recruited to Participate in the Study — 66 Participants
Summary
This study is an NCI-funded, randomized control pilot trial to evaluate: (1) the feasibility and acceptability of a web-based, personalized navigation tool (ConnectedCancerCare) and (2) explore whether the tool improves delivery of team-based survivorship care for women who have recently finished primary breast cancer treatment.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Breast Cancer Patients Successfully Recruited to Participate in the Study |
66 | — |
| SECONDARY Rating the Experience With the CCC Web-based, Survivorship Care Plan |
4.4 | — |
| SECONDARY Percentage of Patients Reporting a Preference for an Oncologist vs. PCP for Their Continuing Cancer Care Services |
0; 3; 5; 14; 23; 25 | — |
| SECONDARY Percentage of Patients Scheduling a Primary Care Physician (PCP) Appointment |
11; 18 | — |
| SECONDARY Patient-Reported Satisfaction With Oncologist/PCP Coordination of Care |
3.1; 3.7 | — |
| SECONDARY Percentage of Patients That Communicated With PCP About Provider Roles |
2; 12 | — |
| SECONDARY Knowledge About Team-based Survivorship Care |
3.4; 3.7 | — |
Eligibility Criteria
Inclusion Criteria
- Diagnosed with early Stage (0-IIB) breast cancer
- Must be a patient of a University of Michigan Breast Cancer Oncologist
- Must be completing primary cancer treatment and transitioning into survivorship
- Must be able to speak, read and write in English
- Must have access and the ability to use the internet
Exclusion Criteria
- Diagnosed with stage III or IV breast cancer
- Unable to speak, read, and write in English
Data sourced from ClinicalTrials.gov (NCT03618017). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.