Feasibility of Remote Activity Assessment and PRO Collection Among Transgender Cancer Survivors

Description

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.

Conditions

Neoplasms, Chronic Disease

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Study Overview

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Study Details

Study overview

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.

Study to Remotely Monitor Activity in Transgender Cancer Survivors

Feasibility of Remote Activity Assessment and PRO Collection Among Transgender Cancer Survivors

Condition
Neoplasms
Intervention / Treatment

-

Contacts and Locations

Los Angeles

Cedars-Sinai Medical Center, Los Angeles, California, United States, 90048

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * 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.
  • * 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.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Cedars-Sinai Medical Center,

Gillian Gresham, PhD, PRINCIPAL_INVESTIGATOR, Cedars-Sinai Medical Center

Study Record Dates

2025-07-01