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Completed

NCT Number: NCT07553156

Mobile Application Versus Tell-show-do Technique for Improved Behavior Management of Dental Anxiety in Children Aged 7-11 Years: a Multicenter Randomized Control Trial in Karachi-Pakistan

This study aims to compare the effectiveness of a mobile application versus the conventional tell-show-do (TSD) technique in reducing dental anxiety among children aged 7-11 years attending their first dental visit. The study is a multicenter randomized controlled trial conducted at tertiary care dental hospitals in Karachi, Pakistan. Participants are randomly assigned to either a mobile application-based behavioral intervention or the TSD technique prior to a dental diagnostic procedure. The primary outcomes include changes in pulse rate and anxiety levels measured using the Raghavendra Madhuri Sujata Pictorial Scale (RMS-PS) before and after the intervention. The findings of this study will help determine whether mobile-based behavioral tools can improve anxiety management in pediatric dental settings.

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Key information

Age range

7 year–11 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Aga Khan University Hospital, Karachi, Sindh, Pakistan

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About this study

Dental anxiety is a common barrier to effective dental care in children and may lead to avoidance of treatment and poor oral health outcomes. Conventional behavioral management techniques such as tell-show-do (TSD) are widely used; however, the increasing availability of digital tools provides an opportunity to enhance patient preparation and reduce anxiety.

This study is a multicenter, open-label, randomized controlled trial conducted at tertiary care dental hospitals in Karachi, Pakistan. Children aged 7-11 years presenting for their first dental visit are enrolled and randomly allocated to either a mobile application-based behavioral intervention or the conventional TSD technique. The intervention is delivered for a standardized duration prior to a dental diagnostic procedure.

The primary outcomes include changes in pulse rate and anxiety levels assessed using the Raghavendra Madhuri Sujata Pictorial Scale (RMS-PS), measured before and after the intervention. Pulse rate is recorded three times at one-minute intervals at each time point and averaged. Secondary analyses include comparison of outcomes between intervention groups.

The study aims to evaluate whether a mobile application can serve as an effective alternative to traditional behavioral techniques in reducing dental anxiety among children in clinical settings.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children aged 7-11 years
  • Children with no prior experience of dental treatment i.e. FDV (first dental visit).

Exclusion criteria

  • Children with any systematic or mental disorder (given the challenges in communication and participation, children with special needs or serious systemic conditions should be prioritized for appropriate care rather than extending their time in the trial)
  • Children who are physically handicapped
  • Children who are undergoing medical treatment or taking any medication that affects the heart rate (it will affect our outcome measure of pulse rate)
  • Children with heart rate related disorders (which could introduce bias to the heart rate results).
  • Children with significant language barriers or special needs that prevent proper communication and understanding.

Treatment and study plan

Mobile application

Behavioral

A mobile application-based behavioral intervention is provided for approximately 5 minutes prior to the dental diagnostic procedure to familiarize children with the dental environment and reduce anxiety.

Tell-Show-Do Technique

Behavioral

The conventional tell-show-do behavioral technique is administered for approximately 5 minutes prior to the dental diagnostic procedure to prepare children and reduce anxiety.

Primary outcomes

  1. Change in Pulse Rate

    Time frame: Before and immediately after intervention and dental diagnosis procedure (within same visit)

    Pulse rate will be measured three times at one-minute intervals before and after the intervention and averaged to assess change.

  2. Change in Dental Anxiety Score (RMS-PS)

    Time frame: Before and immediately after intervention and dental diagnostic procedure (within same visit)

    Dental anxiety will be assessed using the Raghavendra Madhuri Sujata Pictorial Scale (RMS-PS) before and after the intervention. A validated child-friendly anxiety scale based on facial expressions.

Sponsors and collaborators

Lead sponsor

Aga Khan University Hospital, Pakistan

Other

Collaborators

  • Civil Hospital Karachi
  • Dow University of Health Sciences

Registry information

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Apr 27, 2026
Registry last updated
Apr 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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