NCT07542665 Aromatherapy vs Music Therapy for Anxiety in Children During Dental Radiography
| NCT ID | NCT07542665 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Nigde Omer Halisdemir University |
| Condition | Dental Anxiety in Children |
| Study Type | INTERVENTIONAL |
| Enrollment | 100 participants |
| Start Date | 2026-03-05 |
| Primary Completion | 2026-06 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 100 participants in total. It began in 2026-03-05 with a primary completion date of 2026-06.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
This study aims to evaluate and compare the effects of aromatherapy and music therapy on anxiety levels in children undergoing intraoral radiographic examination for the first time. Dental anxiety is a common problem in pediatric patients and can negatively impact cooperation and treatment outcomes. Children included in the study will be randomly assigned to four groups: aromatherapy and music group, aromatherapy group, music therapy group, or control group. In the aromatherapy group, children will be exposed to a selected essential oil (lavender oil) before the radiographic procedure, while in the music therapy group, children will listen to calming music through a speaker. The group receiving both aromatherapy and music therapy will listen to music while being exposed to the essential oil. The control group will receive standard care without any additional intervention. Anxiety levels will be assessed before and after the radiographic procedure using the Facial Imaging Scale (FIS). Simultaneously, pulse rate will be measured before and after the procedure using a finger pulse oximeter. The primary aim is to determine whether aromatherapy, music therapy, or a combination of both is more effective in reducing anxiety compared to the control group. The findings of this study are expected to contribute to the development of simple, non-invasive, and cost-effective methods to improve the comfort and cooperation of pediatric patients during dental radiographic procedures.
Eligibility Criteria
Inclusion Criteria: 1. Children requiring panoramic radiography for dental examination 2. No previous history of dental radiographic procedures 3. Ability to understand and cooperate with the procedure 4. Provision of written informed consent by parents or legal guardians Exclusion Criteria: 1. Presence of hearing or olfactory impairment 2. Use of medications that may affect anxiety levels or heart rate 3. Presence of systemic or neurological disorders 4. Inability to cooperate with the study procedures 5. Refusal of the child or parent/guardian to participate
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07542665 clinical trial?
This trial is open to participants of all sexes, studying Dental Anxiety in Children. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07542665 currently recruiting?
Yes, NCT07542665 is actively recruiting participants. Contact the research team at aycandal@outlook.com for enrollment information.
Where is the NCT07542665 trial being conducted?
This trial is being conducted at Niğde, Turkey (Türkiye).
Who is sponsoring the NCT07542665 clinical trial?
NCT07542665 is sponsored by Nigde Omer Halisdemir University. The trial plans to enroll 100 participants.
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