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Clinical Trials/NCT07191496
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
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

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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