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RecruitingNCT07682714Updated Jul 14, 2026

Capturing Food Intake in Patients Undergoing Radiation Therapy for Cancer

An interventional study of Mobile food record using myCircadian Clock app in Cancer, Radiation Therapy and Dietary Intake, sponsored by University of Minnesota. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-07-14.

Sponsored by University of Minnesota · Not applicable, Interventional, and Other

From the registry’s dates

  • Started Jul 2026; still recruiting 2 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

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.

02

Conditions studied

  • Cancer
  • Radiation Therapy
  • Dietary Intake

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Keywords

  • Mobile food record
  • myCircadian Clock
  • Radiation therapy
  • Cancer patients
  • Nutrition assessment
  • Feasibility study
  • Food logging
  • Smartphone application
03

In context

Neoplasms

9,365 studies on the registry are indexed under Neoplasms; 2,489 are open to participants now.

This study's planned enrollment of 20 is below the median of 50 across 7,253 interventional studies indexed under Neoplasms.

Browse Neoplasms studies →

Lead sponsor

University of Minnesota is the lead sponsor of 1,184 studies on the registry; 195 are open to participants now.

Of its 132 completed or terminated interventional studies of FDA-regulated products, 91 (69%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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 availability for the duration of the study
  • Own a smartphone or smart device
  • Able to read and speak English

Exclusion criteria

Exclusion Criteria:

  • Pregnant or lactating women per self report prior to starting radiation therapy
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (estimated)

Study arms

  • Experimental
    Mobile Food Record

    Participants will use the myCircadian Clock (mCC) app to document all dietary intake throughout the course of their radiation therapy.

    Behavioral: Mobile food record using myCircadian Clock app

Interventions

  • BehavioralMobile food record using myCircadian Clock app

    Participants will use the myCircadian Clock (mCC) app to document all dietary intake. The mCC app serves as a research-based mobile food record by capturing the food image coupled with the participant's free-text entry to self-describe the food. The participants will be asked to document all dietary intake throughout the course of their radiation therapy. All dietary intake will be tracked other than water and medications.

    Also known as: myCircadian Clock app, mCC app

06

What researchers measure

Primary outcomes

  1. Feasibility of completing mobile food record during radiation therapy

    Investigators hypothesize that it is feasible for patients undergoing radiation therapy to comply with completing a mobile food record. Feasibility is defined as 75% of the participants completing the dietary intake on at least 80% of the days that they are undergoing radiation therapy.

    Time frame: Throughout the course of radiation therapy, which can last from 1 to 35 business days.

07

Study locations

1 of 1 sites recruiting
  • University Of Minnesota
    Minneapolis, Minnesota 55455, United States
    • Dr. Lisa Chow, MD,MS · Contact · Chow0007@umn.edu · 612-625-8934
    • Dr. Lindsey Sloan, MD,PhD · Principal investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07682714
Lead sponsor
University of Minnesota
Responsible party
Sponsor
First posted
Jul 6, 2026
Start date
Jul 10, 2026
Primary completion
Aug 22, 2027 (estimated)
Completion
Sep 1, 2027 (estimated)
Last update
Jul 14, 2026

Study contacts

Dr. Lisa Chow, MD, MS
Contact
Chow0007@umn.edu
612-625-8934
Dr. Lindsey Sloan
principal investigator · University of Minnesota

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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