Quality of Life in Breast Cancer Survivors Who Were Pregnant During Their Cancer Treatment
Not yet recruiting
- Conditions
- Breast Cancer SurvivorPregnant WomenQuality of Lifte
- Registration Number
- NCT07191496
- Lead Sponsor
- M.D. Anderson Cancer Center
- 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.
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- Female
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method QOL Questionnaires Through study completion; an average of 1 year
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
MD Anderson Cancer Center
🇺🇸Houston, Texas, United States
MD Anderson Cancer Center🇺🇸Houston, Texas, United StatesEileen Hacker, MDPrincipal Investigator