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Assessing the Time Demands of Cancer

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status

Active, not recruiting

Conditions

Metastatic Breast Cancer
Ovarian Cancer

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT05708703
2022LS100
1R01CA277714-01 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

A total of 80 individuals receiving treatment for metastatic breast or advanced stage ovarian cancer will be asked to complete a baseline survey and install the mobile app on their smartphone; carry the smartphone for 28 consecutive days while outside the home; keep smartphone location and motion services active; confirm and correct (if needed) smartphone-detected activities and trips; use the app interface to provide additional information on activities and trips related to cancer treatment tasks; complete daily surveys regarding well-being; and at the end of the 28 day period, complete an online survey.

Enrollment

78 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years of age or older
  • Diagnosed with advanced stage (III, IV) ovarian (ovarian, fallopian tube or primary peritoneal) or metastatic breast cancer [do not need to be newly diagnosed]
  • Currently receiving any type of therapy for their cancer [can be front-line, maintenance therapy, or treatment for recurrence]
  • Able to complete study tasks in English
  • Able to provide voluntary informed consent
  • Own an Android or iOS smartphone on which the operating system is version 9.0 or higher for Android or 10.0 higher for iOS; or willing to use a researcher-provided smartphone

Exclusion criteria

  • Those who are currently incarcerated
  • Have opted out of research contact

Trial design

78 participants in 1 patient group

Study cohort
Description:
Individuals receiving treatment for metastatic breast cancer or advanced stage ovarian cancer, will complete a baseline survey, install a mobile app on their smartphone to track daily activities, short daily surveys, and a study end survey

Trial documents
2

Trial contacts and locations

2

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Central trial contact

Rachel Vogel

Data sourced from clinicaltrials.gov

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