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Clinical Trials/NCT05162404
NCT05162404
Completed
Not Applicable

Patient-Centered Video Education Intervention to Improve Rural Cancer Care Delivery

University of Hawaii1 site in 1 country14 target enrollmentJanuary 5, 2022
ConditionsCancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cancer
Sponsor
University of Hawaii
Enrollment
14
Locations
1
Primary Endpoint
Changes in rural patients' perceptions of cancer care coordination as assessed by the Care Coordination Instrument at 4-6 months post-intervention.
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this study is to understand if a video-based education program delivered on a tablet device will improve care coordination experiences for patients with cancer living in rural areas.

Registry
clinicaltrials.gov
Start Date
January 5, 2022
End Date
July 1, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
University of Hawaii
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients must have a newly diagnosed Stage I, II, or III disease at the time of enrollment.
  • Patients to be treated with adjuvant chemotherapy or recent initiation of (within 1 month of starting) adjuvant chemotherapy.
  • Patients with a history of previous malignancy treated with chemotherapy within the last 3 years are not eligible, as their perceptions of care coordination may be impacted by their previous treatment.
  • Patients must be ≥ 18 years of age.
  • Patients must be able to read, write, and speak English. Study materials and telephone calls are only available in English.
  • Patients must be residents of Hawaii, Kauai, or Maui counties
  • Patients must be informed of the investigational nature of this study and must sign and give written informed consent in accordance with institutional and federal guidelines.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Changes in rural patients' perceptions of cancer care coordination as assessed by the Care Coordination Instrument at 4-6 months post-intervention.

Time Frame: 6 months

Secondary Outcomes

  • To examine patient demographic and clinical information collected from the background questionnaire as potential correlates of patients' perceptions of cancer care coordination at post-intervention(6 months)
  • Rural patient satisfaction with video education materials as assessed by semi-structured telephone interview.(6 months)

Study Sites (1)

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