Comparison of the effect of braille pamphlet and Audio-tactile Performance Technique on the oral health of visually impaired adolescents

Not Applicable

• Conditions: Evaluating the level of knowledge, attitude, and information about how to deal with dental trauma in visually impaired adolescents..

• Registration Number: IRCT20231025059848N1
• Lead Sponsor: Mashhad University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 January 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

Congenital, totally visually impaired adolescent
bring the parental consent form
Age 10 to 19 years

Exclusion Criteria

Unwillingness to participate in the study

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The level of awareness of the participants in the form of knowledge score. Timepoint: before the intervention and six months after the intervention. Method of measurement: questionnaire.;The level of awareness of the participants in the form of attitude score. Timepoint: before the intervention and six months after the intervention. Method of measurement: questionnaire.;The level of awareness of the participants about how to deal with dental trauma. Timepoint: before the intervention and six months after the intervention. Method of measurement: questionnaire.

Secondary Outcome Measures

Name	Time	Method
Determination of DMFT (Decayed, Missing, Filled Teeth) index. Timepoint: before the intervention three, and six months after the intervention. Method of measurement: Clinical examination.;Determination of OHI (Oral Hygiene Index). Timepoint: before the intervention three, and six months after the intervention. Method of measurement: Clinical examination.;Determination of DI (Debris Index). Timepoint: before the intervention three, and six months after the intervention. Method of measurement: Clinical examination.;Determination of BOP (Bleeding on Probing) index. Timepoint: before the intervention three, and six months after the intervention. Method of measurement: Clinical examination.