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Animal Assisted Therapy Intervention for Hospitalized Patients in a Tertiary Care Center

Not Applicable
Completed
Conditions
Hospitalized Patients
Interventions
Behavioral: Animal Assisted Therapy
Registration Number
NCT02959632
Lead Sponsor
Mayo Clinic
Brief Summary

The purpose of this study is to evaluate the common symptoms leading to an Animal Assisted Therapy consult, and to measure its (AAT) influence on the symptoms and feelings of hospitalized patients.

Detailed Description

Animal Assisted Therapy is being provided by the Caring Canines program and is formally available to patients by referrals. In this study, we would like to capture why patients are being referred and to measure the influence of AAT on the symptoms and feelings of patients.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
21
Inclusion Criteria

Inclusion Criteria (Patients):

  • Patients admitted to St Mary's or Methodist Hospital and subsequently referred for AAT.
  • Subjects undergoing Animal Assisted Therapy as part of their standard care.
  • Patients 18-80 years of age.
  • Patients who are able to read and answer pre and post intervention survey questionnaire and satisfaction survey.

Inclusion Criteria (Care Team Members):

  • Care team members of the study participants.
  • 18-80 years of age.
  • Who are able to read and answer pre and post intervention survey questionnaire and satisfaction survey.
Exclusion Criteria

Exclusion Criteria (Patients):

  • Patients with diagnoses of bipolar disorder, schizophrenia or dementia.
  • Unable to give consent.
  • Pregnant women (as verbalized by participant).

Exclusion Criteria (Care Team Members):

  • Care team members of the study participants who do not want to participate.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Patients receiving AATAnimal Assisted TherapyHospitalized patients receiving Animal Assisted Therapy (AAT). Animal Assisted Therapy (Pet Visit) will be provided to the hospitalized patients.
Primary Outcome Measures
NameTimeMethod
Number of patients scoring improvement of symptoms using the VAS (visual analogue scale)Baseline to 45 minutes

We will record the number of patients scoring improvement of symptoms using the VAS (visual analogue scale).

Secondary Outcome Measures
NameTimeMethod
Number of patients scoring improvement of feelings using the VAS (visual analogue scale)Baseline to 45 minutes

We will record the number of patients scoring improvement of feelings using the VAS (visual analogue scale).

Trial Locations

Locations (1)

Mayo Clinic

🇺🇸

Rochester, Minnesota, United States

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