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Not Yet Recruiting NCT07765069

Positioning in RT - Supine vs. Upright

Conditions: Cancer

Sex: All
Ages: 3 Years – N/A
Healthy volunteers: No
Enrollment: 105
Sponsor: University Health Network, Toronto

Location: Princess Margaret Cancer Centre Toronto Ontario

Summary

This is a single-center, non-therapeutic prospective pilot cohort study evaluating patient-reported comfort levels between upright and supine positioning in patients receiving radiation therapy across all age groups using a concurrent mixed-methods design. Following standard-of-care RT planning or delivery in the conventional supine position, patients and caregivers will complete a questionnaire evaluating the current treatment position. Patients will then be positioned upright in a chair, using similar immobilization to their supine setup when feasible. This position will be maintained for up to 15 minutes, as tolerated by the patient. During the upright positioning session, patients and caregivers will be asked open-ended questions exploring their perceptions of comfort, stability, and overall experience with the upright chair. No radiation or therapeutic intervention will be delivered during the upright session; the upright positioning procedure is non-therapeutic and conducted solely for assessment purposes. Patients and their caregivers will again be asked to complete a questionnaire evaluating the upright position. Key stakeholders involved in RT (including Radiation Therapists, Registered Nurses, Radiation Oncologists, or Medical Physicists), will participate in one semi-structured interview to explore perspectives on supine versus upright positioning for RT. Each interview will take up to 60 minutes and will be conducted in-person or virtual using UHN's Microsoft Teams. All sessions will be audio recorded and transcribed on the UHN Microsoft cloud, which is encrypted and stored securely.

Eligibility Criteria

Inclusion Criteria: 1. Pediatric and adult patients aged 3 years and older, undergoing radiation therapy as part of standard clinical care. 2. Lansky or Karnofsky score 40 or greater 3. Ability to provide informed consent (or if appropriate, provided by parent or legal guardian). 4. Ability to understand and speak English or with appropriate assistance

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07765069). StuddyBuddy aggregates publicly available trial information.