Capturing Food Intake in Patients Undergoing Radiation Therapy for Cancer
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Minnesota
About this trial
The purpose of this study is to determine the feasibility of capturing daily dietary intake of patients undergoing radiation therapy using a mobile food record. This is a prospective single group, non-randomized, feasibility study.
20 participants will be identified during routine clinical care visits with the study PI or co-investigators. Consent will be obtained in person during a clinic visit or using the e-consent process described in section 21.1. They will be asked to use the myCircadian Clock (mCC) app to document their dietary intake for the duration of their radiation treatment. No follow up data will be collected.
Eligibility criteria
Qualifiers
Patients age ≥18 starting a new course of radiation therapy for cancer treatment
Written informed consent obtained from participant and ability for participant to comply with the requirements of the study.
Stated willingness to comply with all study procedures and availability for the duration of the study
Own a smartphone or smart device
Disqualifiers
Pregnant or lactating women per self report prior to starting radiation therapy
Trial design
Treatments tested in this trial
- Mobile food record using myCircadian Clock app
Treatment groups
20 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov