ClinicalTrials.Veeva

Menu

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

M.D. Anderson Cancer Center logo

M.D. Anderson Cancer Center

Status

Begins enrollment this month

Conditions

Breast Cancer Survivor
Pregnant Women
Quality of Lifte

Treatments

Other: Questionnaire

Study type

Observational

Funder types

Other

Identifiers

NCT07191496
NCI-2025-06866 (Other Identifier)
2023-0909

Details and patient eligibility

About

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

Full 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.

Enrollment

50 estimated patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion and exclusion 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

Trial contacts and locations

1

Loading...

Central trial contact

Eileen Hacker, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems