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Understanding and Improving Quality of Life Through a Wireless Activity Tracker: Observational Phase

Understanding and Improving Quality of Life Through a Wireless Activity Tracker: Observational Phase

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02674945
Enrollment
29
Registered
2016-02-05
Start date
2014-09-30
Completion date
2018-09-30
Last updated
2022-06-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain Tumor

Keywords

fitbit, activity tracker, sleep, quality of life

Brief summary

This project attempts to correlate wireless activity data with quality of life and sleep surveys in order to find a new method of monitoring patients during their treatment.

Detailed description

This project proposes the investigation, validation, and use of a wireless activity tracker to better understand and improve the quality of life of patients suffering from brain tumors. The Fitbit flex wireless syncing activity tracker will be distributed to 75 patients, and the electronic infrastructure to automatically track patients will be created and adapted for the cohort. Surveys will routinely assess the ease-of-use and any problems arising. This heterogenous population of patients suffering from brain tumors will be tracked and compared through routine evaluation of their quality of life through well-established surveys, including the SF-36 and FACT-Br. The association between data recorded from the activity tracker and the QOL surveys will be quantified to validate the activity tracking data as a surrogate measure of part, if not all, of QOL as well as sleep.

Interventions

DEVICEWireless Activity tracker: Fitbit

Patients will wear a Fitbit flex

Sponsors

University of Minnesota
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* diagnosed with primary or metastatic brain tumor * able to wear wireless activity tracker * able to complete QOL and sleep surveys every 3 months

Exclusion criteria

* unable to provide consent * age \< 18 * lack of use of the wireless activity tracker for more than 2 consecutive months

Design outcomes

Primary

MeasureTime frame
Activity measured in steps1 year delineated by minute

Secondary

MeasureTime frameDescription
Sleepper night over 1 yearwireless activity will attempt to monitor sleep cycles when the device is worn
Quality of Life - SF-36months 0, 3, 6, 9, and 12SF-36
Quality of Life - Fact- Brmonths 0, 3, 6, 9, and 12Fact-Br

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026