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Changes in Depression and Esthetic Perception After Orthognathic Surgery

Evaluation of Changes in Depressive Symptom Levels and Subjective Esthetic Perception in Patients With Different Types of Malocclusion Following Orthognathic Surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07702448
Enrollment
18
Registered
2026-07-14
Start date
2026-06-20
Completion date
2027-07-20
Last updated
2026-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dentofacial Deformities, Malocclusions, Orthognathic Surgery

Keywords

Orthognathic Surgery, Bimaxillary Surgery, Dentofacial Deformity, Quality of Life, Psychological Outcomes, Beck Depression Inventory-II, Rosenberg Self-Esteem Scale, Orthognathic Quality of Life Questionnaire

Brief summary

This study aims to evaluate changes in depressive symptoms and subjective esthetic perception before and after bimaxillary orthognathic surgery in patients with different types of malocclusion. The study will analyze anonymized clinical data and questionnaire responses to assess the impact of orthognathic surgery on psychological well-being and esthetic perception.

Detailed description

This prospective observational study aims to investigate changes in depressive symptoms and subjective esthetic perception in patients with different types of malocclusion undergoing bimaxillary orthognathic surgery. Participants will be evaluated before surgery and during the postoperative follow-up using validated assessment questionnaires. The study will analyze anonymized data obtained from routine clinical records and patient-reported questionnaires. Variables to be collected include age, sex, occupation, educational level, social media use, and patients' subjective perceptions of esthetics and depressive symptoms. The findings will contribute to a better understanding of the psychological and esthetic outcomes associated with orthognathic surgery and may help optimize patient evaluation and treatment planning.

Interventions

None listed

Sponsors

Kırıkkale University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Adults aged 18 to 40 years. * Individuals without systemic diseases. * Patients with an indication for bimaxillary orthognathic surgery. * Patients who complete the study questionnaires 1 week before surgery and 6 months after surgery. * Individuals who use at least one of the following social media platforms: Instagram, WhatsApp, Snapchat, X, TikTok, or Telegram. * Individuals who provide written informed consent to participate in the study. * Patients scheduled to undergo treatment at the Faculty of Dentistry, Kırıkkale University.

Exclusion criteria

* Patients without an indication for bimaxillary orthognathic surgery or those undergoing single-jaw surgery only. * Individuals with systemic diseases (e.g., diabetes mellitus, hypertension, or thyroid disorders). * Patients with a diagnosed psychiatric disorder. * Patients with a history of previous orthognathic surgery. * Patients scheduled to undergo additional esthetic procedures (e.g., genioplasty, botulinum toxin injection, or dermal filler treatment). * Individuals who decline to participate or do not provide written informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Change in Depressive Symptoms1 week before surgery and 6 months after surgeryChange in depressive symptom scores measured using the Beck Depression Inventory-II (BDI-II) between the preoperative assessment (1 week before surgery) and the postoperative assessment (6 months after surgery). BDI-II is a 21-item self-report instrument used to assess the severity of depressive symptoms. Each item is scored on a scale from 0 to 3, yielding a total score ranging from 0 to 63. Higher total scores indicate greater severity of self-reported depressive symptoms. BDI-II total scores are interpreted as follows: 0-13 indicates minimal, 14-19 mild, 20-28 moderate, and 29-63 severe levels of depressive symptoms.
Change in Quality of Life1 week before surgery and 6 months after surgeryChange in quality of life measured using the Orthognathic Quality of Life Questionnaire (OQLQ) between the preoperative assessment (1 week before surgery) and the postoperative assessment (6 months after surgery). OQLQ is a 22-item self-report instrument developed to assess the impact of dentofacial deformities on patients' quality of life. Each item is scored on a scale from 0 to 4, where a score of 0 indicates that the relevant condition does not bother the patient, while higher scores reflect increasing levels of concern. The item scores are summed to obtain a total score ranging from 0 to 88. Higher total scores indicate a greater negative impact of dentofacial deformity on quality of life and, consequently, poorer quality of life, whereas lower scores indicate better quality of life.
Change in Self-Esteem1 week before surgery and 6 months after surgeryChange in self-esteem scores measured using the Rosenberg Self-Esteem Scale (RSES) between the preoperative assessment (1 week before surgery) and the postoperative assessment (6 months after surgery). RSES is a 10-item self-report instrument developed to assess individuals' global self-esteem and overall sense of self-worth. The scale consists of five positively worded and five negatively worded items, with responses rated on a four-point scale. In the Turkish version adapted by Çuhadaroğlu, responses are evaluated using a Guttman-based scoring system, yielding a total score ranging from 0 to 6. Higher total scores indicate lower levels of self-esteem, whereas lower scores indicate higher levels of self-esteem. Total scores are interpreted as follows: 0-1 indicates high, 2-4 moderate, and 5-6 low levels of self-esteem.

Countries

Turkey (Türkiye)

Contacts

CONTACTElif Assistant Professor, DDS
elifcoban@kku.edu.tr+90 318 224 4927
CONTACTMurat Rıfat Research Asistant, DDS
muratyalinkilic5@gmail.com+90 318 2244927
PRINCIPAL_INVESTIGATORElif Çoban, DDS

Kırıkkale University Faculty of Dentistry

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 17, 2026