Food Intake Tracking for Cancer Radiation Therapy

Capturing Food Intake in Patients Undergoing Radiation Therapy for Cancer

Recruiting N/A Interventional Study
Cancer Radiation Therapy Dietary Intake
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
20 (estimated)
Sponsor
University of Minnesota · Other
Who this trial is looking for

This trial is looking for adults who are starting radiation therapy for cancer. Participants will use an app to track what they eat during their treatment.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am 18 years old or older.
  • I am starting a new course of radiation therapy for cancer.
  • I can give written consent to take part in this study.
  • I own a smartphone or smart device.
  • I can read and speak English.

You may not be able to join if

  • I am pregnant or breastfeeding.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

Check Your Eligibility
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 …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 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 availabi…
Contacts

Dr. Lisa Chow, MD, MS

612-625-8934

Chow0007@umn.edu

CONTACT