Screen to Save: A Colorectal Cancer Educational Intervention (S2S)
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT03907579|
Recruitment Status : Active, not recruiting
First Posted : April 9, 2019
Last Update Posted : April 9, 2019
|Condition or disease||Intervention/treatment||Phase|
|Colorectal Cancer||Behavioral: Inflatable colon educational module||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||100 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Screen to Save: A Colorectal Cancer Educational Intervention|
|Actual Study Start Date :||March 11, 2017|
|Estimated Primary Completion Date :||September 30, 2020|
|Estimated Study Completion Date :||September 30, 2020|
Experimental: Inflatable colon educational module
Participants attend a brief educational presentation in an inflatable colon, focused on colorectal cancer prevention and screening. Participants also receive a copy of the study information sheet and may receive written educational materials to take home. Participants complete a pre-test and a post-test to assess changes in knowledge and intention to get screened for colorectal cancer.
Behavioral: Inflatable colon educational module
Participants attend a brief educational presentation in an inflatable colon, learning about colorectal cancer prevention and screening.
- Change in knowledge related to colorectal cancer risk, prevention, and screening [ Time Frame: Baseline and Immediately following intervention ]A pre-test and post-test is conducted with participants to assess any changes in knowledge related to key learning outcomes expected from the educational intervention (assessed via 14 questions before and after learning).
- Strength of behavioral intentions related to colorectal cancer [ Time Frame: Immediately following intervention ]Post-test conducted to assess behavioral intention related to five prevention and screening behaviors (assessed via 5 questions on a 4-point Likert scale, where a lower score indicates stronger behavioral intention).
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03907579
|United States, New Hampshire|
|Norris Cotton Cancer Center|
|Lebanon, New Hampshire, United States, 03756|