University Hospital Freiburg
In Dr. Alexander Supady
This study will evaluate the effect of a short, animated storytelling intervention video on sodium intake as a major risk factor for cardiovascular disease on immediate and medium-term retention of knowledge about the risks of cardiovascular diesaes due to increased sodium intake. We will also measure voluntary engagement with the content of the short, animated storytelling intervention video on positive psychological capital. In this 4-armed, parallel, randomized controlled trial, 10,000 adult, US participants will be randomly assigned to (1) a short, animated storytelling intervention video on sodium as a cardiovascular disease risk factor followed by surveys assessing the facts om sodium and cardiovascular disease conveyed in the video (2) the surveys only, (3) an attention placebo control video followed by the before mentioned surveys, and (4) an arm that is exposed to neither the video nor the surveys. Two weeks later, participants in all four arms will complete all of the surveys. The primary outcome is knowledge about the cardiovascular disease risk associated with increased sodium intake (immediate and medium-term). The major scondary outcome is the extent of voluntary engagement with the short, animated storytelling video content.
Sodium Excess
Cardiovascular Risk Factor
Education Entertainment Intervention
Short, Animated Storytelling
A short, animated storytelling video on dietary sodium
A short, animated storytelling attention placebo video
NA
| Study Type : | INTERVENTIONAL |
| Estimated Enrollment : | 10000 participants |
| Masking : | TRIPLE |
| Primary Purpose : | PREVENTION |
| Official Title : | A Short, Animated Storytelling Video to Increase Knowledge About Sodium Intake as a Major Cardiovascular Risk Factor and to Give Recommendations for a Low-sodium Healthy Diet: an Online, Randomized, Controlled Trial |
| Actual Study Start Date : | 2023-06-01 |
| Estimated Primary Completion Date : | 2023-07-31 |
| Estimated Study Completion Date : | 2023-08-31 |
Information not available for Arms and Intervention/treatment
| Ages Eligible for Study: | 18 Years to 59 Years |
| Sexes Eligible for Study: | ALL |
| Accepts Healthy Volunteers: | 1 |
Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.
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