Effect on Attendance if Including Focused Information of Spirometry in Preventive Health Checks
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|ClinicalTrials.gov Identifier: NCT02615769|
Recruitment Status : Completed
First Posted : November 26, 2015
Last Update Posted : April 20, 2018
|Condition or disease||Intervention/treatment||Phase|
|Spirometry Patient Participation Health Literacy Lung Diseases||Behavioral: focused information of spirometry in the invitation Behavioral: standard invitation||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||4496 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Effect on Attendance if Including Focused Information of Spirometry in Preventive Health Checks - a Randomized Controlled Trial in Primary Health Care|
|Study Start Date :||November 2015|
|Actual Primary Completion Date :||January 2017|
|Actual Study Completion Date :||January 2017|
|Experimental: Invitation with focused information of spirometry||
Behavioral: focused information of spirometry in the invitation
Focused information of spirometry in the invitation to the preventive health check compose the intervention in this trial.
|Active Comparator: Standard invitition||
Behavioral: standard invitation
The active comparator will receive a standard invitation to the preventive health checks. The preventive health checks in the active comparator group and the intervention group are identical.
- The percentage of participants attending the health check compared between the groups [ Time Frame: one-year recruitment ]Primary outcome measure is effect of the focused information in the invitations on attendance.
- the percentage of participants with abnormal spirometry assessed at the preventive health [ Time Frame: one-year recruitment ]Secondary outcome is the percentage of participants with abnormal spirometry assessed at the preventive health check.
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): NCT02615769
|Institute of public health, section of general practice, Aarhus University|
|Aarhus C, Aarhus County, Denmark, 8000|
|Study Chair:||Annelli Sandbæk, Professor||Institute of public health, section of general practice, Aarhus University|