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SEHAT Virtual Oral Health Promotion for School Adolescents in Pakistan

Evaluating the Impact of Novel Oral Health Promotion Program "SEHAT" Among Adolescents in Pakistan's Resource-Constrained Settings: A Cluster Randomized Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07536958
Acronym
SEHAT
Enrollment
1500
Registered
2026-04-17
Start date
2026-04-01
Completion date
2027-09-01
Last updated
2026-04-22

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

Conditions

Oral Health Behavior Change

Keywords

Oral Hygiene, Oral Health Education, Adolescents, Plaque Score, Gingival Index, Oral Health Promotion, Digital Health, Distant Education, Telehealth

Brief summary

The goal of this cluster-randomized trial is to learn if the SEHAT program works to improve oral health among school adolescents in Pakistan. It will also assess how the program affects oral health behaviors and knowledge. The main questions it aims to answer are: 1. Does the SEHAT program improve toothbrushing behavior and oral hygiene? 2. Does the SEHAT program reduce plaque and gingival scores among adolescents? 3. Does the program improve oral health knowledge and awareness? Researchers will compare the SEHAT virtual intervention with conventional oral health education and a control group to see which approach is most effective. Participants will: 1. Take part in either the virtual SEHAT session or conventional in-person oral health education, or receive no intervention (control) 2. Watch structured 30-minute sessions delivered via Zoom (virtual group) or classroom instruction (conventional group) 3. Participate in follow-up assessments to measure plaque, gingival indices, and oral health knowledge and behaviors.

Detailed description

This study is a cluster randomized trial evaluating the effectiveness of the SEHAT (School-Based Education for Oral Health Awareness Using Advanced Telecommunication Technology) intervention among adolescents aged 11-14 years in public schools in Rawalpindi, Pakistan. The trial aims to improve oral health behaviors, knowledge, and clinical outcomes, including plaque and gingival scores. Schools (clusters) will be randomly assigned to one of three groups: virtual SEHAT intervention, conventional in-person oral health education, or control (no intervention). The virtual intervention will deliver structured 30-minute sessions via Zoom, incorporating interactive elements, culturally relevant content, and reinforcement strategies, while the conventional group will receive the same content through face-to-face classroom instruction. Outcome assessments will include clinical oral health measures (plaque and gingival indices) and self-reported oral health knowledge and behaviors, collected at baseline, post-intervention, and at follow-up timepoints to evaluate short- and medium-term effects. The study will also explore sustained engagement, feasibility, and acceptability of digital oral health education in resource-constrained school settings. This trial addresses gaps in evidence regarding digital oral health interventions in low-resource settings, particularly for adolescents, and will provide data to guide scalable, culturally adapted, school-based oral health promotion strategies.

Interventions

BEHAVIORALSEHAT Virtual Oral Health Education

A structured oral health promotion program delivered virtually using interactive sessions designed to improve oral health knowledge and behaviors.

BEHAVIORALConventional Oral Health Education

Face-to-face classroom-based oral health education using standardized content.

Sponsors

Shifa College of Dentistry
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

This is a cluster randomized, parallel-assignment trial in which school grades (clusters) are randomly assigned to one of three groups: the virtual SEHAT intervention, conventional in-person oral health education, or a control group receiving no intervention. Each cluster receives only the assigned intervention, and outcomes will be compared between groups to evaluate the effectiveness of the interventions on oral health behaviors, knowledge, attitude and clinical measures such as plaque and gingival indices.

Eligibility

Sex/Gender
ALL
Age
11 Years to 15 Years
Healthy volunteers
Yes

Inclusion criteria

For the Schools/grades: * Public high schools situated in the urban and rural areas of the Rawalpindi city, Punjab, Pakistan to account for the regional variations. * Single-gender schools housing classes 6th to 10th. * A minimum total enrollment of 300 - 500 students * A minimum of 30 students per section in the targeted grades (6th, 7th, and 8th). * The schools that sign an agreement to * Participate in the trial * Be randomized to any of the study arms * Assign the trial related tasks to the teachers. For study participants. * Currently enrolled students in 6th, 7th and 8th grades. * Diverse socioeconomic backgrounds * Students with parental and personal informed consent to participate in the trial

Exclusion criteria

* Students currently undergoing active orthodontic treatment. * Students with physical or cognitive impairments that prevent the use of digital interfaces. * Students with systemic medical conditions that manifest as oral health complications.

Design outcomes

Primary

MeasureTime frameDescription
Silness-Löe Plaque IndexBaseline and follow-up assessments at 3, 6, and 12 monthsThe index assigns a score from 0 to 3 based on the amount of plaque present on four surfaces of a tooth. 0 = No plaque in the gingival area. 3 = Abundance of plaque along the gingival margin. Higher scores indicate a worse outcome (greater accumulation of dental plaque).

Countries

Pakistan

Contacts

CONTACTSadia Musharraf, BDS, MCPS, PhD (Candidate)
sadia.scd@stmu.edu.pk92 321 6127576
PRINCIPAL_INVESTIGATORSadia Musharraf, BDS, MCPS, PhD (Candidate)

Shifa College of Dentistry, Shifa Tameer e Millat University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 23, 2026