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Modernizing Instructions to Improve Treatment Participation of Subjects During Their First

Daily patient participation is critical to the successful, life-saving delivery of radiotherapy. There is very little in the literature describing the best way to prepare patients to give optimal participation. This study aims to look at an already-prepared conversion of patient instruction materials and measure whethe

Condition(s)Cancer
StatusRecruiting
PhaseNA
Study typeInterventional
SummaryDaily patient participation is critical to the successful, life-saving delivery of radiotherapy. There is very little in the literature describing the best way to prepare patients to give optimal participation. This study aims to look at an already-prepared conversion of patient instruction materials and measure whether the improvement in clarity and specificity produces the desired changes in patient decision-making and emotional comfort.
Who can participateInclusion 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.
Ages18 Years to 99 Years
SexAll
Lead sponsorUniversity of Florida
LocationsGainesville, Florida, United States
Start date2024-12-24
NCT IDNCT06246409
Official listinghttps://clinicaltrials.gov/study/NCT06246409

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