Ignite Creation Date:
2024-05-05 @ 6:36 PM
Last Modification Date:
2024-10-26 @ 9:35 AM
Study NCT ID:
NCT00519272
Status:
TERMINATED
Last Update Posted:
2020-01-02
First Post:
2007-08-20
Brief Title:
A Prospective Study Examining the Barriers to Care for Harris County Cervical Cancer Patients
Sponsor:
MD Anderson Cancer Center
Organization:
MD Anderson Cancer Center
Study Overview
Official Title:
A Prospective Study Examining the Barriers to Care for Harris County Cervical Cancer Patients
Status:
TERMINATED
Status Verified Date:
2019-12
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Requested by PI during yearly Continuing Review
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 behavioral research study is to look at the reasons that may prevent women from getting early treatment for their cervical cancer
Detailed Description:
Little is known about what prevents women with cervical cancer from getting early and possibly curative treatment This study consists of a series of questionnaires that ask questions about religion coping access to health care physical emotional and spiritual well-being understanding of health questions control fear anxiety and other health beliefs to determine why some women delay coming in for check-ups and why some women do not complete their treatments It is thought that health beliefs influence behavior practices and that by identifying these issues things can be done to improve the health condition and results for these patients
You will be asked to complete a series of questionnaires at 2 specific time points The first time point will be before treatment begins and the second time point will be within a month following completion of treatment
Filling out the questionnaires should take about 45 minutes each time You should have adequate time to complete these questionnaires during your clinic appointment
If you want to take part but are too ill to complete the questionnaires you will be provided a pre-addressed stamped envelope so that you can mail them back to the study staff at your earliest convenience
This is an investigational study This is an investigational study Up to 150 patients will be enrolled at Lyndon B Johnson General Hospital
You will be asked to complete a series of questionnaires at 2 specific time points The first time point will be before treatment begins and the second time point will be within a month following completion of treatment
Filling out the questionnaires should take about 45 minutes each time You should have adequate time to complete these questionnaires during your clinic appointment
If you want to take part but are too ill to complete the questionnaires you will be provided a pre-addressed stamped envelope so that you can mail them back to the study staff at your earliest convenience
This is an investigational study This is an investigational study Up to 150 patients will be enrolled at Lyndon B Johnson General Hospital
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