RecruitingNCT07191496

Quality of Life in Breast Cancer Survivors Who Were Pregnant During Their Cancer Treatment


Sponsor

M.D. Anderson Cancer Center

Enrollment

50 participants

Start Date

Oct 1, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

To assess the quality of life for women who were pregnant during their breast cancer treatment.


Eligibility

Sex: FEMALE

Inclusion Criteria6

  • 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 Criteria3

  • 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

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Interventions

OTHERQuestionnaire

The questionnaires include the Ferrans and Powers QLI, EORTC QLQ-C30, FCR-7 Scale, HADS, and MOS Social Support Survey.


Locations(1)

MD Anderson Cancer Center

Houston, Texas, United States

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NCT07191496


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