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Effect of Vibrasthetic Device on Pain Reduction During Local Anesthesia in Pediatric Patients

Effect of Vibrasthetic Vibration Device on Pain Reduction During Local Anesthesia in Pediatric Patients: A Randomized Clinical Study

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07306650
Enrollment
22
Registered
2025-12-29
Start date
2025-12-26
Completion date
2026-06-30
Last updated
2026-01-02

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

Conditions

Behavior Management, Healthy

Keywords

Vibrasthetic, Vibration, child behavior management, local anesthesia, pediatric dentistry

Brief summary

The goal of this clinical trial is to test if children aged between 6 and 14 years who are receiving a dental injection will feel less pain by using a vibration device applied to the injection site during the injection compared to vibrating the lip using only the researcher's hands without using the vibration device. It will also test if this device makes them feel less anxious during the injection. The main question it aims to answer is: Does using the Vibrasthetic device make dental injections more comfortable for children? Researchers will compare the effect of using this vibration device versus using their hands for manual vibration of the lip in the same child. Participants will: * Experience one method of vibration during their visit to the dentist (either the vibration device or manual vibration). * then after 2 weeks they will go to the same dentist again and experience the other method of vibration. * Receive the dental treatment they need in both visits. Participants will be asked to rate the pain they felt after the injection. This will be done by the participants choosing one of 6 pictures we will show them. Each picture explains the level of the pain they felt, and each picture has a score. We will score the pain the participants felt by looking at which picture they chose to describe their pain from the injection.

Detailed description

Each participant will start their dental appointment by them sitting on a chair beside the dental chair and having their heart rate recorded by a pulse oximeter for baseline comfort level. They will be randomly assigned to either receive the vibration using the Vibrasthetic vibration device or by the dentist researcher manually vibrating the participant's lip during the injection. Topical anesthesia will be applied on the injection site and then they will receive the dental injection along with experiencing vibration in the area of the dental injection administered. Immediately after the injection, the participant will rate the pain intensity felt during the injection using validated Pain Scale (Wong-Baker). During the injection, a separate researcher, called the monitor, will monitor the participant's pain using the FLACC scale (Face, Legs, Activity, Cry, Consolability). Also, the monitor will record the participant's behavior using the Frankl scale, after which the participant will receiver their needed dental treatment. In the following visit, the participant will receive the other vibration method before their dental treatment with the recording of the same metrics by the researchers.

Interventions

Battery powered, no need to replace vibrating head of the unit (only a plastic barrier is required to cover the device), not investigated before.

PROCEDUREManual vibration

The operator will hold the participant's lip between their forefinger and thumb to manually vibrate the lip and hence vibrating the injection site.

Sponsors

King Abdulaziz University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
6 Years to 14 Years
Healthy volunteers
Yes

Inclusion criteria

* Children aged 6-14 years * who have previously received local anesthesia * and whose behavior, according to the Frankl scale, was positive or definitely positive * and the absence of systemic diseases or known allergies to local anesthetic agents

Exclusion criteria

* Uncooperative children * Children with special healthcare needs * Children with conditions affecting pain perception

Design outcomes

Primary

MeasureTime frameDescription
Pain levelParticipant will record the level of pain felt immediately after receiving the injection. This usually occurs around 10 mins after the start of the appointment.Measured subjectively using an Arabic validated Wong-Baker Faces Pain Rating Scale by the participant choosing the picture that best describes the pain they felt. Minimum score is zero, maximum score is 10. Score of zero is the best outcome, which translates into No hurt = no pain felt. Score of 10 is the worst outcome, which translates into Hurts most = severe pain felt

Secondary

MeasureTime frameDescription
Behavior and cooperationThis metric is measured by judging the participant's behavior, and is recorded after the injection is given. This will take around 10 mins from the start of the appointment.Measured using Frankl behavior scale. The investigator monitoring the participant will record the participant's behavior during and after receiving the injection. Behavior can be scored as definitely negative (--), negative (-), positive (+), or definitely positive (++). A score of (--) is the worst outcome, and a score of (++) is the best outcome.

Countries

Saudi Arabia

Contacts

Primary ContactMariam B Aldajani, Master of Dental Science (MDS)
maldajani@kau.edu.sa00966-567808848
Backup ContactGhalia Y Bhadila
gbhadila@kau.edu.sa00966-503637670

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026