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Effect of VR box in reducing pain, anxiety and sensitivity during oral prophylaxis

Phase 2
Completed
Conditions
Health Condition 1: K051- Chronic gingivitis
Registration Number
CTRI/2022/12/047994
Lead Sponsor
Shalini D
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
42
Inclusion Criteria

1.Patients with chronic gingivitis

2. Age: 20 – 40 years

Exclusion Criteria

1.Any systemic illness contraindicating the use of ultrasonic scalers like Chronic pulmonary disease: Asthma, emphysema, cystic fibrosis, pneumonia, Cardiovascular disease with secondary pulmonary disease, Swallowing difficulty

2.Persons with uncontrolled diabetes or hypertension

3.Persons undergoing psychiatric treatment

4.Mentally challenged persons

5.Ophthalmic conditions which contraindicate the use of Virtual Reality box

6. Infectious diseases like HIV, Hepatitis, Tuberculosis (active stages)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Primary outcome of the study is to detect the effect of virtual reality box as a distraction aid in reducing anxiety, pain and sensitivity during oral prophylaxis in adults.Timepoint: 2 months
Secondary Outcome Measures
NameTimeMethod
ILTimepoint: NI
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