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Effect of Personality Traits on Reporting Outcomes of Orthodontic Treatment

NCT05398328 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2023-12-29

No results posted yet for this study

Summary

The study will monitor changes induced by orthodontic treatment and in the retention period, two years after the end of orthodontic treatment. The alignment of teeth, hygiene and gingiva will be assessed. Efficiency of two types of fixed appliances in active phase will be compared - esthetic and metal. Efficiency of two types of retention appliances in retention phase will be compared - fixed and removable.

The benefits of orthodontic treatment to be studied are aesthetic concerns, dental self-confidence, self-esteem, social contacts, psychological influences, and chewing limitation. The stability of personality traits, body image and perfectionism will also be analyzed, as well as the extent to which these dimensions modify the reporting of psychosocial effects of malocclusion treatment.

Conditions

  • Malocclusion

Interventions

DEVICE

active metal appliance

fixed metal labial orthodontic appliance MBT 0.022'' slot

DEVICE

active esthetic appliance

fixed ceramic labial orthodontic appliance MBT 0.022'' slot

COMBINATION_PRODUCT

retention fixed appliance

fixed lingual metal retention appliance

COMBINATION_PRODUCT

retention removable appliance

removable clear termoplastic retention appliance

Sponsors & Collaborators

  • University of Rijeka

    lead OTHER

Principal Investigators

  • Stjepan Spalj, PhD · Sveuciliste u Rijeci

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
SEQUENTIAL

Eligibility

Min Age
13 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-11-01
Primary Completion
2026-01-01
Completion
2026-03-01

Countries

  • Croatia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05398328 on ClinicalTrials.gov