- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06464003
Orthodontic Screening in Public Healthcare
July 4, 2025 updated by: Heidi Arponen, University of Helsinki
Orthodontic Screening and Treatment Need in Public Health Care
The aim of the study is to examine orthodontic screening practises in public health care.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
The study aims to assess repeatability of malocclusion evaluation in orthodontic treatment need screening in a publicly funded clinic.
The objective treatment need is compared with subjective need for orthodontic treatment.
Study Type
Observational
Enrollment (Estimated)
350
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Heidi Arponen
- Phone Number: +3582941911
- Email: Heidi.arponen@helsinki.fi
Study Contact Backup
- Name: Heidi Arponen
- Phone Number: +3582941911
Study Locations
-
-
-
Helsinki, Finland, FI-00014
- Recruiting
- University of Helsinki
-
Contact:
- Heidi Arponen, DDS
- Email: heidi.arponen@helsinki.fi
-
Vantaa, Finland, 01030
- Recruiting
- Vantaa and Kerava Wellbeing Services County
-
Contact:
- Heidi Arponen
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Unselected population sample study
Description
Inclusion Criteria:
- residence in the wellbeing services county catchment area
- willingness to participate in the study
Exclusion Criteria:
- Age under 6 years or over 16 years
- insufficient language skills to be able to understand the questionnaire
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Treatment need
Individuals with objective treatment need
|
Malocclusion impact questionnaire
|
|
No treatment need
Individuals with no objectively determined treatment need
|
Malocclusion impact questionnaire
|
|
Controls
Random sample of individuals
|
Malocclusion impact questionnaire
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Treatment need
Time Frame: Baseline
|
Orthodontic treatment need
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Subjective evaluation
Time Frame: Baseline
|
A questionnaire enquiring subjective evaluation of the treatment need and impact of malocclusion on oral heath related quality of life
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Heidi Arponen, University of Helsinki
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 6, 2024
Primary Completion (Estimated)
June 6, 2026
Study Completion (Estimated)
June 6, 2026
Study Registration Dates
First Submitted
June 6, 2024
First Submitted That Met QC Criteria
June 14, 2024
First Posted (Actual)
June 18, 2024
Study Record Updates
Last Update Posted (Estimated)
July 8, 2025
Last Update Submitted That Met QC Criteria
July 4, 2025
Last Verified
July 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- UHelsinki
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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