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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05207137
Other study ID # Cristin-ID: 2526531
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 3, 2021
Est. completion date June 30, 2022

Study information

Verified date January 2022
Source Norwegian Institute of Public Health
Contact Marit Tuv, MD
Phone +47 97566647
Email marit.tiv@fhi.no
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators will randomise individuals from family doctors' lists of patients that are at risk of severe Coronavirus Disease 2019 (COVID-19), and that are not registered as having taken the vaccine against the disease. The patients will be randomised to receiving a phone call from their family physician where the participants are given the opportunity to raise questions they might have around vaccination. The investigators will assess whether this has an impact on vaccine uptake.


Recruitment information / eligibility

Status Recruiting
Enrollment 400
Est. completion date June 30, 2022
Est. primary completion date April 28, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Belonging to group at risk of severe COVID-19 Exclusion Criteria: -

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Telephone call about vaccination
Participants receive phone call from their family physician, where they are invited to ask questions about the COVID-19 vaccine.

Locations

Country Name City State
Norway Bolteløkka legesenter Oslo

Sponsors (2)

Lead Sponsor Collaborator
Norwegian Institute of Public Health City of Oslo, Norway

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Vaccination status (COVID-19) Change in proportion of participants who are registered in the national vaccination registry, as having received at least one dose of a COVID-19 vaccine. 3-6 weeks after inclusion
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