Dog-Assisted Therapy in Children During Blood or Dental Extraction. (Extra-can)

September 8, 2025 updated by: Esther Rodrigo Claverol, Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina

Efficacy Study of Dog-Assisted Therapy in Children During Blood or Dental Extraction: Extra-can Project

The purpose of the present study is to evaluate the efficacy of Animal Assisted Therapy (AAT) during blood extraction or dental procedures in a Primary Care Pediatric Service. Determine the improvement in facilitating the task of venipuncture or dental extraction for nursing or dental professionals. Estimate the reduction in the child's emotional stress during these procedures with the support of a therapy dog. Evaluate the emotional stress in the accompanying family member. These objectives will be accomplished through a randomized open label two-arm controlled study of AAT for children who need a blood or dental extraction.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

INTRODUCTION: Venous puncture for routine blood sampling can be distressing for many children, leading to heightened anxiety both before and during the procedure. Dental anxiety affects around 9% of European children and adolescents, potentially persisting into adulthood and resulting in dental avoidance behaviors. Animal-assisted therapy (AAT) is viewed as a distraction technique that could play a vital role in managing pain and distress for children. AAT is a planned, structured therapeutic intervention with specific goals, facilitated by healthcare professionals.

OBJECTIVES: Evaluate the efficacy of AAT during blood or dental extraction in a Primary Care Pediatric Service. Determine the improvement in facilitating the task of venipuncture or dental extraction for nursing or dental professionals. Estimate the reduction in the child's emotional stress during these procedures with the support of a therapy dog. Evaluate the emotional stress in the accompanying family member.

METHODOLOGY: Randomized two-arm clinical trial (control group and intervention group) involving children aged 3 to 8 requiring blood analysis or dental extraction in a Primary Health Care Center. Patients will be randomly assigned to the control and intervention groups. Sample size calculations suggest 60 patients in each group to detect statistically significant differences. The control group follows standard protocols, while the intervention group includes AAT with 10 minutes of pre-procedure interaction with the therapy dog, extraction performed with the therapy dog, and 5 minutes of post-procedure interaction. Personnel includes nurses or dentists, a pediatrician, and an AAT technician. Response variables include various scales measuring anxiety and distress, while control variables encompass age, gender, pathologies, extraction type, and pet ownership.

EXPECTED RESULTS: The implementation of AAT as an emotional support intervention, utilizing a therapy dog for distraction, is anticipated to improve symptomatology in the intervention group by reducing fear and anxiety post-procedure.

Study Type

Interventional

Enrollment (Estimated)

120

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Lleida, Spain, 25000
        • Recruiting
        • Centre d'Atenció Primària Primer de Maig
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Age between 3 and 12 years old.
  • Need a blood or dental extraction.
  • Willing to participate in the study on a voluntary basis.
  • Delivery of the information sheet and signature the informed consent.

Exclusion Criteria:

  • If in the initial interview they declared having allergy or fear of dogs.
  • Have aggression disorder towards dogs.
  • Not want to participate in the study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Control group
The control group underwent a blood and dental extraction will be performed according to the usual protocol of the health center.
Blood and dental extraction will be performed according to the usual protocol of the health center in both groups; with the additional assistance of the therapy dog in experimental group.
Other Names:
  • Dog Assisted Therapy
Experimental: experimental group

The experimental group underwent a blood and dental extraction will be performed according to the usual protocol of the health center, the same as control group, and in addition dog-assisted therapy will be performed.

Intervention (with the additional assistance of the therapy dog). Includes AAT with 10 minutes of pre-procedure interaction with the therapy dog, extraction performed with the therapy dog, and 5 minutes of post-procedure interaction.

Blood and dental extraction will be performed according to the usual protocol of the health center in both groups; with the additional assistance of the therapy dog in experimental group.
Other Names:
  • Dog Assisted Therapy

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Observation Scale of Behavioral Distress (OSBD) registered at baseline, during and immediately after the intervention
Time Frame: This scale registered behaviors in continuous 15-second intervals at baseline, during and immediately after the intervention
Is an instrument for measuring children's distress during painful medical procedures, assessed by an external observer. It is a 4-point Likert-type scale instrument (where the numerical values are weighted from 0 (not at all) to 3 (very much)) that evaluates 11 different behaviors
This scale registered behaviors in continuous 15-second intervals at baseline, during and immediately after the intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
State-Trait Anxiety Inventory Questionnaire (STAI) registered at baseline and immediately after the intervention
Time Frame: This questionnaire will be administered at baseline and immediately after the intervention, post-extraction.
Is a self-administered questionnaire that assesses the levels of clinical anxiety (both trait anxiety ("most of the time") and state anxiety ("at the present moment")). The total score on each of the subscales ranges from 0 to 60 points.
This questionnaire will be administered at baseline and immediately after the intervention, post-extraction.
Wong-Baker Faces Scale registered at baseline and immediately after the intervention
Time Frame: This scale will be administered at baseline and immediately after the intervention, post-extraction.
Is a tool that uses a combination of faces, numbers, and words to help a person effectively communicate the severity of their physical pain. A 0 point 'happy face' represents the absence or lack of pain. A 10 point 'crying face' represents the worst possible or most excruciating pain. All the faces in between represent a scoring of 2, 4, 6, or 8, respectively, based on the pain severity facial image chosen.
This scale will be administered at baseline and immediately after the intervention, post-extraction.

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluation questionnaire for health professionals administered immediately after the intervention
Time Frame: This questionnaire will be administered immediately after the intervention, post-extraction

This is a questionnaire that will be completed by the professionals (nursing or dentist) at the end of the intervention. Using a Likert scale from 0 to 10 (0= Not at all and 10= A lot). It contains the following questions:

  • Did you find it stressful to do the extraction? (CG+EG)
  • How relaxed you have seen the child? (CG+EG)
  • How calm have you seen the parents? (CG+EG)
  • Did the presence of the dog make the extraction easier? (EG)
  • Do you consider that the dog reduces the risk of accidents during extraction? (EG)
  • Has the presence of the dog interfered with your work? (EG)
This questionnaire will be administered immediately after the intervention, post-extraction
Parent satisfaction questionnaire administered immediately after the intervention
Time Frame: This questionnaire will be administered immediately after the intervention, post-extraction

The following questions will be asked in writing and answered by parents.Using a Likert scale from 0 to 10 (0= Not at all and 10= A lot). It contains the following questions:

  • Have you experienced this procedure (extraction) in a stressful way? (CG+EG)
  • How relaxed have you seen the child? (CG+EG)
  • In terms of satisfaction, how would you rate this procedure? (CG+EG)
  • Has the presence of the dog made the child feel calmer? (EG)
  • Has the presence of the dog made you feel calmer? (EG)
  • Do you think that the child has experienced the extraction as a less aggressive activity because of the presence of the dog? (EG)
  • Would you recommend this experience to other parents to do with their children? (EG)
This questionnaire will be administered immediately after the intervention, post-extraction

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Marta Ortega Bravo, PhD, IDIAP Jordi Gol

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2022

Primary Completion (Estimated)

November 30, 2025

Study Completion (Estimated)

December 30, 2025

Study Registration Dates

First Submitted

June 9, 2024

First Submitted That Met QC Criteria

June 18, 2024

First Posted (Actual)

June 21, 2024

Study Record Updates

Last Update Posted (Estimated)

September 15, 2025

Last Update Submitted That Met QC Criteria

September 8, 2025

Last Verified

September 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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