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Clinical Trials/NCT05089201
NCT05089201CompletedNot Applicable

A Pilot Study to Examine the Impact of a Therapy Dog Intervention on Loneliness and Related Health Outcomes in Vulnerable Populations

Virginia Commonwealth University1 site in 1 country72 target enrollmentStarted: November 16, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
72
Locations
1
Primary Endpoint
Attrition rate

Study Overview

Brief Summary

The purpose of this research study is to test whether an animal-assisted interaction (AAI) intervention is better than conversation with another person or treatment as usual for improving mood, anxiety, loneliness, quality of life, and indicators of health care services such as number of hospitalizations, length of hospital stay, and cost of services. Participants will be patients admitted for an inpatient stay at Virginia Commonwealth University Health who meet the study entry requirements.

Detailed Description

Participants will be randomly assigned (like the flip of a coin) to receive one of the following interventions:

  1. Animal-assisted interaction (a dog-handler team will visit them in their hospital room)
  2. Conversational interaction with just participants and the handler
  3. Treatment as usual (the regular services patients are currently receiving in the hospital)

Participation in this study will last six months. This includes the three days on which participants will receive one of the interventions described above, plus completing some questionnaires online or by phone one month and six months after the baseline visit. These questionnaires will ask questions about pet ownership, relationship with pets participants have had, loneliness, depression, anxiety, health-related quality of life, significant life events in the past year, and social supports. Approximately 180 individuals will participate in this study.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •18 years of age or older
  • •Projected to be admitted to the hospital for the upcoming four days
  • •Speak English
  • •Able to provide consent.

Exclusion Criteria

  • •Fear of, or allergy to, dogs
  • •Documented contact precautions
  • •Cognitive impairment that prevents consent or completion of measures.

Arms & Interventions

Animal-assisted interaction (AAI)

Experimental

Dogs and handlers will visit with patients for 20 minutes and discuss semi-scripted topics.

Intervention: Animal-assisted interaction (Behavioral)

Conversational interaction

Active Comparator

Handlers will have a 20 minute semi-scripted conversation with patients.

Intervention: Conversational control (Behavioral)

Treatment as usual

No Intervention

Patients will receive treatment as usual.

Outcomes

Primary Outcomes

Attrition rate

Time Frame: 30 months

Number of participants who do not complete the full study

Number of participants enrolled

Time Frame: 2 years

The number of eligible patients who sigh consent forms and are randomized to a condition

Secondary Outcomes

  • Change in loneliness(Baseline to 6 months)
  • Change in anxiety(Baseline to 6 months)
  • Change in depression(Baseline to 6 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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