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Testing Video Information About Mammography Screening

Testing Video Information About Mammography Screening in a Randomized Design

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04424758
Enrollment
400
Registered
2020-06-11
Start date
2020-06-16
Completion date
2020-07-30
Last updated
2020-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Brief summary

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

Detailed 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.

Interventions

OTHERVideo information about mammography screening

A video informing about mammography screening

OTHERVideo information about smart energy systems

A video informing about smart energy systems

Sponsors

University of Copenhagen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

See protocol

Intervention model description

See protocol

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Participants eligible for the study includes all men and women age 18-75.

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Choice: proportion of participants in favor of mammography screeningOne monthThe primary outcome in the study is choice. A possible effect of the intervention on choice will be examined by comparing the proportion of participants in favor of screening (on the individual level and societal level respectively) between the intervention arm and the control arm. One question addressing the societal choice and one question addressing the individual choice is included in our questionnaire.

Secondary

MeasureTime frameDescription
Response duration: timeOne monthResponse duration is registered for all participants in the online survey. Mean response duration will be calculated in both the intervention arm and control arm.
Acceptability of the video: percentage of participants finding the video to be neutral, in favor of or against mammography screening.One monthPercentages of the participants finding the video to be neutral, in favor of or against mammography screening will be calculated in the intervention arm.

Countries

Denmark

Contacts

Primary ContactManja Jensen, MD
madj@sund.ku.dk0045-35333123
Backup ContactJohn Brodersen, MD, PhD
jobr@sund.ku.dk0045-35333123

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026