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CTNow: A Clinical Trials Education Program for Rural Cancer Patients and Oncology Providers

CTNow: A Clinical Trials Education Program for Rural Cancer Patients and Oncology Providers

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06237816
Enrollment
50
Registered
2024-02-02
Start date
2025-05-01
Completion date
2026-12-01
Last updated
2026-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer, Oncology

Brief summary

The overall goal of the project is to pilot test CTNow, a multilevel intervention designed to facilitate access and referrals to cancer clinical trials in rural areas through patient and provider education and teleconference resources.

Interventions

OTHERPatient Education Intervention

Multimedia Educational Videos

OTHERProvider Education Intervention

Provider workshops via zoom

Sponsors

University of Hawaii
Lead SponsorOTHER
Agency for Healthcare Research and Quality (AHRQ)
CollaboratorFED

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients must have been diagnosed with any cancer. * Patients who have received treatment, are receiving cancer treatment at the time of enrollment, or estimated to start treatment within 90 days. * 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.

Exclusion criteria

* Patients must not have previously participated in a cancer clinical trial. Those who have participated in a cancer clinical trial are not eligible for the study.

Design outcomes

Primary

MeasureTime frameDescription
Change in patients' awareness and knowledge of clinical trials18 monthsParticipants will complete a 12-item awareness and knowledge of clinical trials questionnaire at baseline and post-intervention. Items are reported on a Likert-type scale , with higher scores indicating greater knowledge. A paired t-test will be used to evaluate whether there is a statistically significant difference in pre- and post-intervention scores on patients' knowledge of clinical trials.

Countries

United States

Contacts

CONTACTIzumi Okado, PhD
iokado@cc.hawaii.edu(808) 564-5978
CONTACTAaron Roberts
aroberts@cc.hawaii.edu8084404583
PRINCIPAL_INVESTIGATORIzumi Okado, PhD

University of Hawaii Cancer Research Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 30, 2026