- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06468111
Dog-Assisted Therapy in Children During Blood or Dental Extraction. (Extra-can)
Efficacy Study of Dog-Assisted Therapy in Children During Blood or Dental Extraction: Extra-can Project
Study Overview
Status
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
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Esther Rodrigo Claverol, MD
- Phone Number: 0034973272446
- Email: erodrigo.lleida.ics@gencat.cat
Study Contact Backup
- Name: Esther Rodrigo Claverol, MD
- Phone Number: 0034977272446
- Email: erodrigo.lleida.ics@gencat.cat
Study Locations
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Lleida, Spain, 25000
- Recruiting
- Centre d'Atenció Primària Primer de Maig
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Contact:
- Esther Rodrigo Claverol, MD
- Phone Number: 0034973272446
- Email: erodrigo.lleida.ics@gencat.cat
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
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
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 |
|---|---|
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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.
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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:
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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:
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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
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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
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This scale registered behaviors in continuous 15-second intervals at baseline, during and immediately after the intervention
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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.
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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.
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This questionnaire will be administered at baseline and immediately after the intervention, post-extraction.
|
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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.
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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.
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This scale will be administered at baseline and immediately after the intervention, post-extraction.
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Evaluation questionnaire for health professionals administered immediately after the intervention
Time Frame: This questionnaire will be administered immediately after the intervention, post-extraction
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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:
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This questionnaire will be administered immediately after the intervention, post-extraction
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Parent satisfaction questionnaire administered immediately after the intervention
Time Frame: This questionnaire will be administered immediately after the intervention, post-extraction
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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:
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This questionnaire will be administered immediately after the intervention, post-extraction
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Collaborators and Investigators
Collaborators
Investigators
- Study Director: Marta Ortega Bravo, PhD, IDIAP Jordi Gol
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- DMP ID: 2163
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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