Improving patient instructions for first-time radiotherapy
Modernizing Instructions to Improve Treatment Participation of Subjects During Their First Radiotherapy
NA · University of Florida · NCT06246409
This study is testing whether clearer instructions for first-time radiotherapy patients can help them feel more comfortable and involved in their treatment.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 650 (estimated) |
| Ages | 18 Years to 99 Years |
| Sex | All |
| Sponsor | University of Florida (other) |
| Locations | 1 site (Gainesville, Florida) |
| Trial ID | NCT06246409 on ClinicalTrials.gov |
What this trial studies
This study focuses on enhancing the clarity and specificity of patient instruction materials for individuals undergoing their first external beam radiotherapy. By modernizing these instructions, the research aims to assess whether improved communication can lead to better patient decision-making and increased emotional comfort during treatment. The study will compare the effects of the new instructional materials against existing ones to determine their impact on patient participation. The ultimate goal is to ensure that patients are better prepared and more engaged in their treatment process.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who are preparing for their first external beam radiotherapy.
Not a fit: Patients who have previously received external beam radiotherapy or those undergoing inpatient treatment may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved patient participation and comfort during radiotherapy, potentially enhancing treatment outcomes.
How similar studies have performed: While there is limited literature on this specific approach, similar studies have shown that improved patient communication can enhance treatment participation and outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients ≥ 18 years old planning their first external beam radiotherapy * Written informed consent obtained from the subject and the subject agrees to comply with all the study-related procedures. Exclusion Criteria: * Have received external beam radiotherapy in the past * External beam radiotherapy is initiated as inpatient. * External beam radiotherapy consists of less than 3 fractions. * Planned radiotherapy that does not employ an external beam * Planned participation in a clinical study that prohibits participation in a second, concurrent treatment trial * Prisoners or subjects who are involuntarily incarcerated, or subjects who are compulsorily detained for treatment of either a psychiatric or physical illness.
Where this trial is running
Gainesville, Florida
- University of Florida — Gainesville, Florida, United States (RECRUITING)
Study contacts
- Principal investigator: Alexandra De Leo, MD — University of Florida
- Study coordinator: Amy Carrao-Tackett
- Email: amy.carrao-tackett@ufhealth.org
- Phone: 352-265-8826
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Cancer, patient comfort, patient participation, external beam radiotherapy, radiation oncology