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The Impact of an Animal-assisted Activity on the Stress Level of Hospitalized Children

The Impact of an Animal-assisted Activity on the Stress Level of Hospitalized Children: a Randomized Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04663815
Enrollment
14
Registered
2020-12-11
Start date
2021-04-01
Completion date
2021-06-30
Last updated
2021-10-07

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

Conditions

Hospitalization in Children

Brief summary

The aim of this research is to study the effect of an animal-assisted activity (AAA) on the stress level of hospitalized children.

Detailed description

A hospitalization is a major stressor in a child's life, which can have negative effects on recovery. It is assumed that animal-assisted interventions can have a positive effect on the level of stress, but this has not yet been sufficiently researched. This study aims to measure a possible effect. Children who are hospitalized will receive an animal-assisted activity. A normal afternoon in their hospital room counts as a control activity. The stress level is measured through saliva cortisol, blood pressure, heart rhythm variability and a visual analogue stress scale.

Interventions

The intervention is an animal-assisted activity consisting of a visit to Villa Samson (a place on the campus of the hospital specifically intended for patients to meet pets), where the child will work with a therapy dog for 1 hour. Under supervision, the animal is stroked and combed by the child, they play games together, the child feeds the animal, etc.

OTHERControl intervention

The control intervention reenacts a normal stay in the hospital, so the child spends one hour in the hospital room where the child can play, watch tv, etc.

Sponsors

Universitair Ziekenhuis Brussel
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Randomized clinical trial.

Eligibility

Sex/Gender
ALL
Age
6 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* hospitalized in the Universitair Ziekenhuis Brussel * dutch and/or french speaking.

Exclusion criteria

* decreased immunity * multi-resistant germs * disturbed diabetes * fever of unknown origin * fear of animals * dogs or cats allergy * cognitive impairment

Design outcomes

Primary

MeasureTime frameDescription
Change in visual analogue stress scale1 hourA 10-point scale for patient self-reporting of stress. The scale ranges from 0-10 where 0 indicates a better and 10 indicates a worse outcome.
Change in systolic and diastolic blood pressure1 hourA marker of the activity of the sympathetic nervous system.
Change in saliva cortisol1 hourA marker of the activity of the hypothalamic - pituitary - adrenal axis.
Change in heart rate variability (HVR)1 hourA marker of the activity of the sympathetic nervous system.

Countries

Belgium

Outcome results

None listed

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