Hospitalized Patients Clinical Trial
Official title:
Animal Assisted Therapy Intervention for Hospitalized Patients in a Tertiary Care Center: A Pilot Study
NCT number | NCT02959632 |
Other study ID # | 16-007730 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | November 2016 |
Est. completion date | July 30, 2020 |
Verified date | January 2021 |
Source | Mayo Clinic |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 21 |
Est. completion date | July 30, 2020 |
Est. primary completion date | July 30, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | 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. |
Country | Name | City | State |
---|---|---|---|
United States | Mayo Clinic | Rochester | Minnesota |
Lead Sponsor | Collaborator |
---|---|
Mayo Clinic |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of patients scoring improvement of symptoms using the VAS (visual analogue scale) | We will record the number of patients scoring improvement of symptoms using the VAS (visual analogue scale). | Baseline to 45 minutes | |
Secondary | Number of patients scoring improvement of feelings using the VAS (visual analogue scale) | We will record the number of patients scoring improvement of feelings using the VAS (visual analogue scale). | Baseline to 45 minutes |
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