Breast Cancer Clinical Trial

Reproductive Health Survivorship Care Plan Pilot

Summary

Most young breast cancer patients undergo chemotherapy and/or endocrine therapy, treatments that impair ovarian function and result in significant reproductive health late effects. These late effects include symptoms of estrogen deprivation (e.g., hot flashes and vaginal dryness), which are distressing in young breast cancer survivors (YBCS). The goal of this pilot study is to test the feasibility of a 4-week text message based intervention on hot flashes and vaginal dryness in YBCS. YBCS will be randomized in a 1:1 ratio to the intervention (text messages on hot flash and vaginal dryness management) and control arms. All participants will be prompted to provide daily hot flash frequency and severity via text messaging. The primary hypothesis is YBCS will have high rates of daily hot flash reporting via text messaging. Secondarily, we will compare changes in hot flash frequency, hot flash severity and vagina dryness between the intervention and control arms.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Breast cancer
Female
Completed primary breast cancer treatment
Age <=45

Study is for people with:

Breast Cancer

Estimated Enrollment:

38

Study ID:

NCT02176083

Recruitment Status:

Completed

Sponsor:

University of California, San Diego

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There is 1 Location for this study

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UC San Diego
La Jolla California, 92093, United States
UCSD Moores Cancer Center
La Jolla California, 92093, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

38

Study ID:

NCT02176083

Recruitment Status:

Completed

Sponsor:


University of California, San Diego

How clear is this clinincal trial information?

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