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Animal Assisted Therapy in Dentistry (AAT)

University of North Carolina (UNC) logo

University of North Carolina (UNC)

Status

Completed

Conditions

Anxiety

Treatments

Other: Dog Therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT04708028
19-1911

Details and patient eligibility

About

A cross-sectional prospective study measuring physiologic biometrics and perceptions of stress during a dental procedure with or without a therapy dog present.

Full description

Patients will be consented, enrolled, and assigned to a control group (no dog) or to an experimental group (dog). The patient assigned to the experimental group will be exposed to the therapy animal prior to the dental appointment. Pre-dental procedure and post-dental procedure surveys will be given to all the subjects asking the same questions. Biometric data will be collected by measuring heart rates of the patient/subject during the dental appointment with a Shimmer or Polar device.

Enrollment

40 patients

Sex

All

Ages

7 to 17 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria: Subjects must meet all of the following inclusion criteria to be eligible for enrollment in the study:

  • 7-17 years of age
  • Patient undergoing 1 quadrant restorative dental procedure requiring a handpiece (e.g. multiple fillings, sealants and/or stainless-steel crowns) and/or extraction(s)
  • History of moderate dental anxiety with a Frankl score of 2-3 based on Epic chart review

Exclusion Criteria Subjects presenting with any of the following will not be included in the study:

  • Patients with developmental delay/special needs, Autism Spectrum Disorders (ASDs), craniofacial defects, chronic pain conditions, and/or dental syndromes
  • No history of dental anxiety
  • Moderate to severe allergy to dogs
  • Previous traumatic experience with a dog and/or self-reported fear of dogs
  • Patients who are not receiving dental care requiring a handpiece (for ex, prophylaxis only)
  • Patients with severe, documented xerostomia
  • Patients receiving sedation (pharmacological and conscious sedation) or general anesthesia
  • Patients who will have physical restraints placed during the dental procedure
  • Patient scheduled to have sedation or general anesthesia
  • Severe acute or chronic medical or psychiatric condition(s) that would interfere with the interpretation of results, and in the judgement of the Investigator, would make the subject inappropriate for entry into the trial
  • Patient with developmental/cognitive disability that cannot self-assent, comprehend and follow the requirements of the study based on research site personnel's assessment.
  • Inability or unwillingness of individual and legal guardian/representative to give written informed assent (from child) and consent (from adult).

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

Control
No Intervention group
Description:
No exposure to the therapy dog.
Dog Therapy
Experimental group
Description:
Introduced to a therapy dog and allowed to pet the dog for up to 2 minutes (timed) prior to the dental procedure.
Treatment:
Other: Dog Therapy

Trial documents
2

Trial contacts and locations

1

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Central trial contact

Laura A jacox, DMD, PhD, Ms; S.T. Phillips, BSDH

Data sourced from clinicaltrials.gov

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