| Registry | NCT07191496 |
|---|---|
| Status | Terminated - <75% participation |
| Study type | Observational |
| Enrollment | 30 (Actual) |
| Sponsor | M.D. Anderson Cancer Center (Other) |
| Conditions | Breast Cancer Survivor, Pregnant Women, Quality of Lifte |
| Interventions | Questionnaire (Other) |
| Dates | start 2025-10-01, primary completion 2026-04-09, completion 2026-04-09, first posted 2025-09-24, last updated 2026-04-17 |
| Locations | 1 site in United States |
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To assess the quality of life for women who were pregnant during their breast cancer treatment.
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.
Sex: Female
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
| Facility | City | Country | Status |
|---|---|---|---|
| MD Anderson Cancer Center | Houston, Texas | United States |