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Investigating Public Enthusiasm for Mammography Screening in Denmark

University of Aarhus logo

University of Aarhus

Status

Completed

Conditions

Decision Making
Breast Neoplasm Female
Mammography Screening
Information Seeking Behavior

Treatments

Behavioral: Information about hypothetical mammography screening without benefits

Study type

Interventional

Funder types

Other

Identifiers

NCT04509063
2016-051-000001, 1835

Details and patient eligibility

About

Based on an American study by Scherer et al., it is hypothesized that some women will make irrational choices regarding their participation in mammography screening. Therefore, the aim is to estimate the prevalence of Danish women having an irrational preference for mammography screening even when it confers no benefits, but only harms.

Full description

The prevalence of women making an irrational decision will be compared to the participation rate in the Danish screening program. The study population will consist of a random sample of women aged 44-49. Similar to the American study, two types of information will be compared (detailed vs. non-detailed information about the harms of screening). Participants will be randomised to one of two information groups. Based on the American study, it is assumed that the willingness to participate in the hypothetical screening program will be 40 percent. To achieve the desired precision in this study, a standard error of 2.5 percent is required corresponding to a confidence interval spanning approximately 35-45 percent. This will require 384 women in each group, corresponding to a total study population of 768. The survey will be sent electronically (using "e-Boks") with a link to access the online survey trial. The survey will consist of screening and cancer related questions as well as questions on age, education, and health literacy. Five questions on appraisal of health information from the Health Literacy Questionnaire will also be included. After the data collection, data will be linked to data on income, residence, civil status, education, breast cancer diagnosis, and information on whether a participant is immigrant, descendent or of Danish origin.

The original plan for the main analysis was to compare the two groups of women randomized to different information groups (detailed vs. non-detailed information about the harms of screening). However, due to lower participation rate and therefore smaller sample size than expected, information group was disregarded in the main analysis. The two groups will still be compared in a secondary analysis. This decision was made before getting access to data from the questionnaire.

Enrollment

768 patients

Sex

Female

Ages

44 to 49 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Residence: Central Denmark Region

Exclusion criteria

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

768 participants in 2 patient groups

Detailed information about screening harms
Other group
Treatment:
Behavioral: Information about hypothetical mammography screening without benefits
Non-detailed information about screening harms
Other group
Treatment:
Behavioral: Information about hypothetical mammography screening without benefits

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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