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Care Coordination Educational Intervention Study for Patients from Rural Areas with Early Stage Cancer

U

University of Vermont Medical Center

Status

Enrolling

Conditions

Cancer

Treatments

Other: Table-based Educational Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT05723250
00002358

Details and patient eligibility

About

Care Coordination is an essential component of cancer care delivery. Many patients experience poor care coordination. In this study, we hypothesize that provision of a video educational intervention to teach patients about cancer, care coordination and self-advocacy will improve patients' perception of care coordination. Cancer patients with early stage disease scheduled to receive adjuvant therapy, and who reside in a rural area, will be enrolled onto the study. Patients will be randomized to receive a table-based educational intervention tool initially (arm1) or after 4 months of therapy (arm2). Assessment of cancer knowledge, self-advocacy and care coordination will be obtained at baseline and after 4-6 months.

Enrollment

40 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18+ years of age
  • Breast, lung, or colon cancer diagnosis
  • Stage I, II or III cancer
  • Adjuvant chemotherapy started < 30 days or planned within the next 30 days
  • Rural residence location in Vermont (outside Chittenden County)
  • Proficient in English

Exclusion criteria

  • History of prior malignancy treated with chemotherapy in last 3 years
  • Known or suspected neuro-cognitive impairment
  • Resident of Chittenden County, Vermont
  • Patients with current diagnosis other than stage I, II or III breast, colon or lung cancer

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Upfront Educational Intervention
Experimental group
Description:
Participants will receive a video-based intervention after completing baseline survey instruments and prior to retesting after 4-6 months.
Treatment:
Other: Table-based Educational Intervention
Delayed Educational Intervention
Experimental group
Description:
Participants will complete baseline survey instruments and again complete surveys after 4-6 months. They will then receive the video-based educational tablet.
Treatment:
Other: Table-based Educational Intervention

Trial contacts and locations

1

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Central trial contact

Randall F Holcombe

Data sourced from clinicaltrials.gov

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