Assisted Animal Therapy: ReAnimal

NCT03898843 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 7

Last updated 2023-05-26

No results posted yet for this study

Summary

Assisted animal therapy (AAT) is getting more and more used worldwide, in such areas as gerontology, psychiatry, or oncology. It is a complementary therapy, and benefits for patients are various, including decrease of anxiety. In ICU, some case reports exist, but no study has ever been made in order to prove its benefits, not even its feasibility.

In ReAnimal, the investigator aims to compare a group of patients receiving assisted animal therapy, versus a group of patients not receiving it. Primary objective will be the evolution of anxiety scores between the 2 groups of patients. Secondary objectives will be the comparison of mood scores, post traumatic stress syndrome scores, pain scores, and physiologic parameters such as blood pressure, cardiac frequency. The investigating team will also compare multi drug resistant bacteria incidence between the 2 groups. In the assisted animal therapy group, patients will also be asked to answer a satisfaction questionnaire.

Conditions

  • Anxiety
  • Mood Disorders
  • Post Traumatic Stress Disorder

Interventions

OTHER

Animal assisted therapy

Patients of AAT group will leave their hospital bedroom to go in the session room, where they will meet a dog, who has come with his veterinary student master. Animal assisted therapy session will last at most 20 minutes, in which the patient is going to interact with the dog, pet him, play with him, etc.

BIOLOGICAL

Nasal swab sampling

All patients will have nasal swab sampling at inclusion and 7 days after AAT session or sham session in order to screen multidrug resistant bacteria

BEHAVIORAL

STAI-Y and POMS Questionnaires

Before and after AAT or sham session, patients will answer State-Trait Anxiety Inventory Y (STAI-Y), Profile of Mood States (POMS) questionnaires.

PROCEDURE

physiological parameters measure

Before and after AAT or sham session, blood pressure, heart rate dans respiratory rate will be measured.

OTHER

Visual Analog Scale (VAS)

Before and after AAT or sham session, pain will be evaluated thanks to VAS

BEHAVIORAL

Impact of Event Scale - Revised (IES-R)

Patients will answer IES-R questionnaire 3 months after AAT or sham session

BEHAVIORAL

satisfaction questionnaire

Patients of the AAT group will answer satisfaction questionnaire at the end of the AAT session and 3 months after AAT

BIOLOGICAL

Rectal swab sampling

All patients will have rectal swab sampling at inclusion and 7 days after AAT session or sham session in order to screen multidrug resistant bacteria

Sponsors & Collaborators

  • Hospices Civils de Lyon

    lead OTHER

Principal Investigators

  • Guillaume PETIT, MD · Hospices Civils de Lyon

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-09-18
Primary Completion
2022-08-24
Completion
2022-08-24

Countries

  • France

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03898843 on ClinicalTrials.gov