CARE-BI:a Pilot Study to Improve Patient Comfort and Reduce Psychological Distress During IA Removal

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorM.D. Anderson Cancer Center

About this trial

The goal of this research study is to learn about the rate of posttraumatic stress disorder (PTSD) experienced by women after undergoing gynecologic brachytherapy.

Eligibility criteria

Qualifiers

Capable of signing informed consent

Age ≥ 18 years old

Receipt of multiple intracavitary brachytherapy treatments for gynecologic cancer

Capable of completing PRO and patient satisfaction surveys and willing to comply with completion of surveys multiple times throughout and after treatment

Disqualifiers

Patients without ability to sign informed consent

Patients unwilling or unable to complete PRO and patient satisfaction surveys at the times required by the study

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed

Sponsors and collaborators