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Non-pharmacological Interventions for Dental Anxiety in Adult Patients in Oral Medicine Dentistry

Non-pharmacological Interventions for Dental Anxiety in Adult Patients in Oral Medicine Dentistry

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095507
Enrollment
Unknown
Registered
2025-01-08
Start date
2025-01-20
Completion date
Unknown
Last updated
2025-01-13

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

Conditions

Dental anxiety

Interventions

Experimental group:Music, health education video or games based on XR devices
Control group:Standard care

Sponsors

Stomatological Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age: 18 years old or older. 2.Dental treatment needs: First oral medical treatment, such as filling, root canal treatment, periodontal treatment, etc. 3.Health condition: In good physical health, without any serious chronic diseases or acute infections. 4.Cognitive ability: sufficient cognitive ability to understand and sign informed consent forms. 5.Communication skills: Ability to communicate effectively and understand research processes and requirements. 6.Willingness to cooperate: Volunteer to participate in research and commit to comply with research regulations.

Exclusion criteria

Exclusion criteria: 1.The presence of severe visual impairment, photosensitive epilepsy, or other health problems that may affect the intervention. 2.Myopia is more than 600 degrees. 3.Are using medications that may affect cognitive or emotional states (e.g., sedatives, antidepressants). 4.Are receiving other dental treatments or interventions that may have affected the study results. 5.Inability to understand the language used in the study or communication difficulties. 6.Have serious mental health problems, such as severe depression and anxiety. 7.Female participants were pregnant or breastfeeding during the study period. 8.Duration of dental treatment >=1 hour.

Design outcomes

Primary

MeasureTime frame
Anxiety;

Secondary

MeasureTime frame
Blood pressure, heart rate, oxygen saturation;Pain;

Countries

China

Contacts

Public ContactZeng Yang

Stomatological Hospital of Chongqing Medical University

772111224@qq.com+86 23 88860121

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026