Purpose of this Study
We are doing this study to develop and test a nurse-delivered program for women who are experiencing premature and early menopause after cancer. The study's program includes personalized menopause health education and skills training to help manage menopause symptoms.
Who Can Participate?
Eligibility
Women ages 18-44 who:
- Are cancer survivors
- Completed their last round of therapy at least 12 months ago
- Have not menstruated (had a period) in the past 12 months
Age Range
18-44
Sex/Genders
Female (cisgender)
Non-binary or gender fluid
Looking for Healthy Participants
No
What is Involved?
Description
There are three phases to this study. Different participants will be recruited for each different phase of the study. If you choose to take part in this study, you will participate in whichever phase is enrolling at the time you choose to join.
Phase 1: If you participate in this phase, you will complete a one-on-one interview with a study team member to learn more about the impact and challenges of managing premature or early menopause after cancer. You will also review our proposed program and share your feedback and opinions.
Phase 2: If you participate in this phase, you will enroll in the program, which has been refined from the feedback given in Phase 1. The program's visits will take place on Zoom with the study therapist over the course of about 10 weeks. You will fill out surveys before and after going through the program. We will also ask you to do an exit interview with a study team member to share feedback about the program and your experience after it is over.
Phase 3: If you participate in this phase, you will get a random assignment (like a coin flip) to either go through the study program or get the standardized health education on life after cancer treatment. We will also ask you to do an exit interview with a study team member to share feedback about the program or the health education you received and your experience after it is over.
Locations
Remote/online
Compensation
Yes
Spanish Materials Available
No
Study Details
Full Title
JUST-IN-TIME REQUEST: Improving outcomes for women experiencing premature or early menopause after cancer: development and pilot testing of a novel intervention
Principal Investigator
Rebecca
Shelby
Protocol Number
PRO00117811
NCT ID
NCT06982677
Enrollment Status
Pending Open to Enrollment