NCT07191496TerminatedNot Applicable
Quality of Life in Breast Cancer Survivors Who Were Pregnant During Their Cancer Treatment
M.D. Anderson Cancer Center1 site in 1 country30 target enrollmentStarted: October 1, 2025Last updated:
Trial Snapshot
- Phase
- Not Applicable
- Status
- Terminated
- Sponsor
- M.D. Anderson Cancer Center
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- QOL Questionnaires
Study Overview
Brief Summary
To assess the quality of life for women who were pregnant during their breast cancer treatment.
Detailed Description
Primary Objectives Provide preliminary data to describe the current QOL of breast cancer survivors who received cancer treatment while pregnant.
Secondary Objectives Identify the relationship between QOL and anxiety, depression, fear of cancer recurrence, and social support in breast cancer survivors, who received treatment while pregnant.
Study Design
- Study Type
- Observational
- Observational Model
- Case Crossover
- Time Perspective
- Cross Sectional
Eligibility Criteria
- Sex
- Female
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Eligibility Criteria
- •Female, any current age and any age at diagnosis
- •Documented diagnosis of breast cancer during pregnancy
- •Documentation of receiving chemotherapy during pregnancy
- •Alive with no evidence of disease at time of recruitment
- •Able to reach and speak English
Exclusion Criteria
- •Any woman who delayed and received their chemotherapy after delivery.
- •Any woman who was diagnosed with breast cancer before or after their pregnancy.
- •Any woman whom there is documentation of inability to provide consent in the medical record
Outcomes
Primary Outcomes
QOL Questionnaires
Time Frame: Through study completion; an average of 1 year
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (1)
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