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Clinical Trial Summary

This study examines how video information about mammography screening effect participants knowledge opinions and choice about screening.


Clinical Trial Description

This study will be conducted as a single site parallel-arm, 1:1 randomized controlled trial (RCT) through a web-based quantitative survey uploaded in online forums. Participants will be randomized to either the intervention group (video information about mammography screening followed by a survey about mammography screening) or the control group (video information about energy systems followed by the same survey). The survey computer programme will randomly assign each respondent to either the intervention arm or the control arm in the beginning of the survey.

The allocation will be concealed from the researchers. The survey computer programme will deliver the intervention right after randomization. Participants will be aware of the allocation. However, they do not know about the study design. Data analysts will be kept blinded to the allocation.

Choice, knowledge and opinions related to mammography screening will be compared between the control group and the intervention group at one timepoint. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04424758
Study type Interventional
Source University of Copenhagen
Contact Manja Jensen, MD
Phone 0045-35333123
Email madj@sund.ku.dk
Status Recruiting
Phase N/A
Start date June 16, 2020
Completion date July 30, 2020

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