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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06237816
Other study ID # Okado-2023-2
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 2024
Est. completion date December 2025

Study information

Verified date May 2024
Source University of Hawaii
Contact Izumi Okado, PhD
Phone (808) 564-5978
Email iokado@cc.hawaii.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 35
Est. completion date December 2025
Est. primary completion date July 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Patient Education Intervention
Multimedia Educational Videos
Provider Education Intervention
Provider workshops via zoom

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
University of Hawaii Agency for Healthcare Research and Quality (AHRQ)

Outcome

Type Measure Description Time frame Safety issue
Primary Change in patients' awareness and knowledge of clinical trials Participants 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. 18 months
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