Patient Centered Outcomes Research Institute (PCORI) Provider Survey on Treatment Eligibility
Status: | Recruiting |
---|---|
Conditions: | Colorectal Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/21/2016 |
Start Date: | December 2014 |
Contact: | George Chang, MD, MS |
Phone: | 713-792-6940 |
Objectives:
1. Determine the surveillance practice patterns following curative resection of colorectal
cancer
2. Identify patient characteristics related to eligibility for treatment after the
detection of a colorectal cancer recurrence
1. Determine the surveillance practice patterns following curative resection of colorectal
cancer
2. Identify patient characteristics related to eligibility for treatment after the
detection of a colorectal cancer recurrence
A survey related to surveillance practice patterns following curative resection of
colorectal cancer patients will be administered to eligible providers for them to complete.
The survey collects basic information related to a providers' role in in colorectal care in
addition to their perspective on patient characteristics that may directly influence a
patients' ability to receive treatment for a recurrent colorectal cancer.
The surveys may be self-administered and completed anonymously, either in a hard copy or
electronic formats. They may also be administered by the research personnel in a group
setting for paper or electronic surveying. The surveys may be sent to providers as in PDF
form for respondents to print and complete, handed out in person, emailed as a qualtrics
study or electronically administered at a regularly occurring conference for colorectal
cancer physicians. In the case the survey is electronically administered in a group setting,
audience response equipment will be used. Individual data will be collected using electronic
response devices. No personally identifying information will be collected. Participants will
not be identifiable using data collected in these group settings. If the form is handed out
in person, it will be given out and collected using a blank envelope to eliminate any way of
identifying the provider completing it.
If respondents print and complete paper forms they will be ask to return them with no
identifying information. Participants will be asked to place the deidentified survey in a
sealed envelope and return through mail or in a drop-box placed in a common location, all
envelopes returned to the study staff in person will be collected together and opened in
aggregate. Electronically administered questionnaires, using audience response or a
qualtrics survey, will have no identifying information.
colorectal cancer patients will be administered to eligible providers for them to complete.
The survey collects basic information related to a providers' role in in colorectal care in
addition to their perspective on patient characteristics that may directly influence a
patients' ability to receive treatment for a recurrent colorectal cancer.
The surveys may be self-administered and completed anonymously, either in a hard copy or
electronic formats. They may also be administered by the research personnel in a group
setting for paper or electronic surveying. The surveys may be sent to providers as in PDF
form for respondents to print and complete, handed out in person, emailed as a qualtrics
study or electronically administered at a regularly occurring conference for colorectal
cancer physicians. In the case the survey is electronically administered in a group setting,
audience response equipment will be used. Individual data will be collected using electronic
response devices. No personally identifying information will be collected. Participants will
not be identifiable using data collected in these group settings. If the form is handed out
in person, it will be given out and collected using a blank envelope to eliminate any way of
identifying the provider completing it.
If respondents print and complete paper forms they will be ask to return them with no
identifying information. Participants will be asked to place the deidentified survey in a
sealed envelope and return through mail or in a drop-box placed in a common location, all
envelopes returned to the study staff in person will be collected together and opened in
aggregate. Electronically administered questionnaires, using audience response or a
qualtrics survey, will have no identifying information.
Inclusion Criteria:
1. Subjects are physicians or other providers who work in the Gastrointestinal and
Colorectal Centers at MD Anderson Cancer Center OR are a member or guest of the
ALLIANCE for Clinical Trials for Oncology OR academic and community providers to
patients with colorectal cancer
2. Subjects are trained to provide care to colorectal cancer patients
3. Subjects are at least 18 years of age and have adequate command of English language
Exclusion Criteria:
We found this trial at
1
site
1515 Holcombe Blvd
Houston, Texas 77030
Houston, Texas 77030
713-792-2121
University of Texas M.D. Anderson Cancer Center The mission of The University of Texas MD...
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