Feasibility of Remote Activity Assessment and PRO Collection Among Transgender Cancer Survivors
Recruiting now
Conditions studied: Neoplasms, Chronic Disease
In brief
Prospective observational feasibility study to evaluate the role of wearable activity monitors to determine the feasibility and acceptability of remote monitoring using wearable technology and PROs to monitor fatigue and physical function in transgender cancer patients and survivors.
Key facts
- Study ID
- NCT05391217
- Run by
- Cedars-Sinai Medical Center
- People needed
- 20
- Starts
- 2023-02-01
- Expected to finish
- 2025-07-01
- Last updated by the study team
- 2024-08-27
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Self-identifies as transgender person with a history of cancer or receiving treatment for cancer in the last five years from screening for the current study (case) OR self-identifies as transgender person without a history of cancer (control)
- 18 years or older
- Ambulatory (use of walking aids, such as cane and rollator, is acceptable)
- Access to a device (e.g., smartphone, tablet, iPhone) that has the capability to sync to the Fitbit
- Have an understanding, ability, and willingness to fully comply with study procedures and restrictions
- Can read and understand English, Spanish, or Tagalog (for participant surveys and interviews)
- Informed consent obtained from subject and ability for subject to comply with the requirements of the study.
You may not qualify if…
- Any person that does not meet the listed criteria above
- Using a pacemaker, implantable cardiac defibrillator, neurostimulator, implantable hearing aids, cochlear implants, or other electronic medical equipment*. However, removable hearing aids are permitted.
Where it is running
- Cedars-Sinai Medical Center — Los Angeles, California, United States (enrolling)
Full record on ClinicalTrials.gov
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