Skip to main content
Clinical Trials/NCT04727749
NCT04727749
Completed
Not Applicable

A Study of the Pawsitive Impacts of Therapy Dog Visits With Adult Emergency Department Pain Patients

University of Saskatchewan1 site in 1 country211 target enrollmentJune 7, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain
Sponsor
University of Saskatchewan
Enrollment
211
Locations
1
Primary Endpoint
Change in Pain Score
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The goal of this unique 18 month study is to better understand the experiences of pain patients in the Royal University Hospital (RUH) Emergency Department (ED), to create excellence in health care. The purpose is to measure the impact of visiting therapy dogs on reducing ED patient pain.

Detailed Description

The goal of this unique 18 month study is to better understand the experiences of pain patients in the Royal University Hospital (RUH) Emergency Department (ED), to create excellence in health care. The purpose is to measure the impact of visiting therapy dogs on reducing ED patient pain. The background rationale is that pain is the primary reason individuals attend an ED, patient pain is generally not well managed in EDs, Saskatchewan EDs have among the longest wait times in the country, and anxiety associated with ED waiting can negatively impact patients' pain. Research suggests a therapy dog can change patients' perceptions of pain and its intensity and facilitate relaxation. The intervention will be examined for its impact on patients' sensory pain (i.e., physical pain severity), affective pain (i.e., emotional pain unpleasantness) and anxiety. It is important to find creative, low-cost ways to respond to patients attending the ED for pain. The primary objective of this study is to generate new health-related knowledge on the ED pain patient experience. The secondary objectives are to implement effective end-of-grant knowledge translation and dissemination strategies and undertake a successful model of collaborative, multidisciplinary research among researchers, patient advisors and system representatives, rooted in a One Health framework.

Registry
clinicaltrials.gov
Start Date
June 7, 2019
End Date
September 20, 2019
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Colleen Dell

Research Chair in One Health & Wellness, Professor, Tenured

University of Saskatchewan

Eligibility Criteria

Inclusion Criteria

  • Over the age of 18
  • Able to provide consent
  • Attending the Emergency Department because of pain/discomfort
  • Canadian Triage and Acuity Score (CTAS) of 2-5
  • Willing to visit with a therapy dog team (intervention group only)

Exclusion Criteria

  • Pain medications (specifically immediate release acetaminophen and opioid analgesics) within an hour prior to the visit

Outcomes

Primary Outcomes

Change in Pain Score

Time Frame: Baseline visit compared to 20 minutes post-visit

Pain score using the Edmonton Symptom Assessment System (revised version) (ESAS-r) 11-point rating scale (scale of 0 to 10), in which higher ratings indicate worse outcomes.

Number of Participants Stratified by Edmonton Symptom Assessment System (Revised Version) (ESAS-r) Pain Scores

Time Frame: 20 minutes post visit

Participants Stratified by Pain scores Edmonton Symptom Assessment System (revised version) (ESAS-r) 11-point rating scale (scale of 0 to 10), in which higher ratings indicate worse outcomes, Pain Scores at 20 Minutes Post Visit.

Secondary Outcomes

  • Number of Participants Stratified by Edmonton Symptom Assessment System (Revised Version) (ESAS-r) Depression Scores(20 minutes post-visit)
  • Number of Participants Stratified by Edmonton Symptom Assessment System (Revised Version) (ESAS-r) Well-Being Scores(20 minutes post-visit)
  • Number of Participants Stratified by Edmonton Symptom Assessment System (Revised Version) (ESAS-r) Anxiety Scores(20 minutes post-visit)
  • Change in Blood Pressure(20 minutes post-visit)
  • Change in Heart Rate(20 minutes post-visit)

Study Sites (1)

Loading locations...

Similar Trials