A Pilot Study of Remote Monitoring to Improve Health Related Quality of Life of Men Following Prostate Cancer Treatment.



Status:Recruiting
Conditions:Prostate Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:Any
Updated:2/17/2019
Start Date:July 11, 2018
End Date:December 2019
Contact:Nicole Zahradka, PhD
Email:nzahrad1@jhu.edu
Phone:516-526-3395

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The purpose of this study is to determine the feasibility of using digital technology and
remote monitoring to track health-related measures in men following prostate cancer
treatment. Half of the participants will receive tools to monitor their activity and weight,
as well as personalized feedback on these measures, while the other half will receive
standard of care. Health related quality of life measure will be collected from both groups.

The purpose of this study is to determine the feasibility of using digital technology and
remote monitoring to track health-related measures in men following prostate cancer
treatment. All participants will complete a health-related quality of life survey each month
for 3 months. The digital survey will be administered on a programmed tablet. The
participants in the intervention group will also receive an activity sensor and weight scale.
Health state data from this group will be generated over a 3-6 month period and remotely
monitored. These data will be used to provide personalized feedback regarding the
participant's progress towards established goals. Health-related quality of life will be
compared between participants in the intervention group, who receive (1) tools to monitor
their activity and weight and (2) personalized feedback, versus participants in the control
group, who receive standard of care. The potential improved adherence to healthy behaviors of
the participants receiving personalized feedback may translate to to improved health-related
quality of life.

Inclusion Criteria:

- Participants must have localized prostate cancer.

- Participants must have received treatment at Johns Hopkins

- Participants must be classified as overweight (body mass index ≥ 25).

- Participants must have wi-fi in their homes.

Exclusion Criteria:

- Anyone who is unable to give informed consent will be excluded

- Anyone who is physically unable to participate in physical activity will be excluded.
We found this trial at
1
site
1800 Orleans St.
Baltimore, Maryland 21287
410-955-5000
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