Ignite Creation Date:
2024-05-06 @ 3:19 AM
Last Modification Date:
2024-10-26 @ 11:32 AM
Study NCT ID:
NCT02263014
Status:
COMPLETED
Last Update Posted:
2022-07-01
First Post:
2014-10-08
Brief Title:
Psychosocial Outcomes and Contralateral Prophylactic Mastectomy CPM
Sponsor:
MD Anderson Cancer Center
Organization:
MD Anderson Cancer Center
Study Overview
Official Title:
Treatment Decisions and Breast Cancer Psychosocial Outcomes
Status:
COMPLETED
Status Verified Date:
2022-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this research study is to learn more about how different treatment decisions may influence the quality of life in women with breast cancer Researchers want to use what is learned from this study to help future patients with breast cancer to be more informed when making treatment decisions
Detailed Description:
With your verbal permission you may have been asked to complete a questionnaire about your surgical treatment preferences for breast cancer as part of initial screening for this study This takes about 5 minutes to complete
If you agree to participate in this study during the same visit you will complete a questionnaire about your background such as your education level marital status and family history of cancer This should take about 3 minutes to complete
You will also be asked to complete a questionnaire about your surgery decisions and your feelings about those decisions at the following times around the time you enroll in study before your surgery and again about 1 6 and 12 months after the surgery is completed This questionnaire should take about 30-40 minutes to complete each time You may complete this questionnaire at the clinic or you may complete it at home If you chose to complete the questionnaire at home you will be given a postage-paid envelope to mail it back to the study staff
Length of Study
After you complete all of the questionnaires your participation in this study will be over
This is an investigational study
A total of up to 345 participants will be enrolled in this study Up to 245 will take part at MD Anderson and up to 100 will take part at Kelsey-Seybold
If you agree to participate in this study during the same visit you will complete a questionnaire about your background such as your education level marital status and family history of cancer This should take about 3 minutes to complete
You will also be asked to complete a questionnaire about your surgery decisions and your feelings about those decisions at the following times around the time you enroll in study before your surgery and again about 1 6 and 12 months after the surgery is completed This questionnaire should take about 30-40 minutes to complete each time You may complete this questionnaire at the clinic or you may complete it at home If you chose to complete the questionnaire at home you will be given a postage-paid envelope to mail it back to the study staff
Length of Study
After you complete all of the questionnaires your participation in this study will be over
This is an investigational study
A total of up to 345 participants will be enrolled in this study Up to 245 will take part at MD Anderson and up to 100 will take part at Kelsey-Seybold
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None