Ignite Creation Date:
2024-05-05 @ 11:09 PM
Last Modification Date:
2024-10-26 @ 10:29 AM
Study NCT ID:
NCT01269645
Status:
COMPLETED
Last Update Posted:
2016-06-08
First Post:
2010-12-22
Brief Title:
Facts and Attitudes About Clinical Trials
Sponsor:
H Lee Moffitt Cancer Center and Research Institute
Organization:
H Lee Moffitt Cancer Center and Research Institute
Study Overview
Official Title:
Evaluating Educational Materials About Cancer Clinical Trials
Status:
COMPLETED
Status Verified Date:
2016-06
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:
FACT
Brief Summary:
The primary objective of this project is to examine the impact of providing cancer patients with audiovisual information about clinical trials on attitudes towards clinical trial participation It is hypothesized that patients provided these materials will have more favorable attitudes toward clinical trial participation compared to patients not provided these materials
Participants will be randomized to either 1 an intervention condition in which they will be asked to view a short video and read an accompanying brochure about clinical trials developed by the investigative team or 2 a control condition in which they will be asked to read the National Cancer Institutes brochure entitled Taking Part in Cancer Treatment Research Studies Self-report data will be collected at two timepoints 1 in person following study enrollment but before receipt of material related to intervention assignment baselineTime 1 and 2 by telephone interview between 7 and 28 days following study enrollment follow-upTime 2 In addition data will also be collected from medical records six weeks after study enrollment
Participants will be randomized to either 1 an intervention condition in which they will be asked to view a short video and read an accompanying brochure about clinical trials developed by the investigative team or 2 a control condition in which they will be asked to read the National Cancer Institutes brochure entitled Taking Part in Cancer Treatment Research Studies Self-report data will be collected at two timepoints 1 in person following study enrollment but before receipt of material related to intervention assignment baselineTime 1 and 2 by telephone interview between 7 and 28 days following study enrollment follow-upTime 2 In addition data will also be collected from medical records six weeks after study enrollment
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None