Breast Cancer Survivor, Pregnant Women, Quality of Lifte
Conditions
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.
Interventions
OTHERQuestionnaire
The questionnaires include the Ferrans and Powers QLI, EORTC QLQ-C30, FCR-7 Scale, HADS, and MOS Social Support Survey.
Sponsors
M.D. Anderson Cancer Center
Study design
Observational model
CASE_CROSSOVER
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
FEMALE
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| QOL Questionnaires | Through study completion; an average of 1 year |
Countries
United States
Contacts
PRINCIPAL_INVESTIGATOREileen Hacker, MD
M.D. Anderson Cancer Center
Outcome results
None listed