Skip to content

Comparison of Physical Versus Visual Distraction in the Reduction of Pain During Local Anesthesia

Comparison of Physical Versus Visual Distraction in the Reduction of Pain During Local Anesthesia

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04595721
Enrollment
0
Registered
2020-10-20
Start date
2022-03-31
Completion date
2022-07-31
Last updated
2022-04-20

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

Conditions

Pain

Keywords

Dental pain

Brief summary

The purpose of this study is to compare physical versus visual distractions to determine which technique reduces perceived pain better during local anesthesia injections.

Detailed description

Before the local anesthesia injection, patients will be asked to give a preliminary VAS score based on what level of pain 0-10 they anticipate they will feel during the local anesthesia injection. Following the injection the participant will be asked to quantify the pain felt during the injection on a 0-10 Visual analog scale (VAS). The VAS scores will only be taken from the first injection of the appointment. Participants will be asked their gender, race, age, geographic location they spent most of their lives as well. Participants will be de-identified and randomly assigned a number that will be recorded along with their collected data on a two-factor, password protected web server. Information collected during this study may be used for further analysis and publication.

Interventions

BEHAVIORALHidden object

Participant will be instructed to look at the hidden object image on the overhead light to look for a number of objects and observe the image.

BEHAVIORALStress ball

Participants will be handed a single-use, squeezable stress ball and instructed to squeeze the stress ball.

Sponsors

Virginia Commonwealth University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients needing a dental procedure that requires a buccal infiltration with Septocaine 1:100,000 epinephrine (EPI) (Articaine hydrochloride 4% and EPI 1:100,000) or an inferior alveolar nerve block injection with 2% lidocaine with 1:100,000 epinephrine. * Adults greater than 18 years old. * Patients with limited English proficiency will be included only if their primary language is Spanish.

Exclusion criteria

* Patients with a known or suspected allergy to anesthetic agent, sulfites, amide-type local anesthetic, or to any ingredient in anesthetic solutions will not be included. * Any patients taking medications affecting pain response on the day of the dental appointment. * Children younger than 18 years old. * Patients with limited English proficiency with a primary language other than Spanish

Design outcomes

Primary

MeasureTime frameDescription
Change in painUp to 30 minutesParticipants will be asked to rate their pain on a visual analog pain scale. The scale is rated from 0 (no pain) to 10 (pain as bad as it can be)

Outcome results

None listed

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