Companion Dog Walking for ICU Survivor Health (POOCH)

Feasibility and Acceptability of a Randomized Controlled Trial Comparing a Companion Dog-Walking Intervention to an Attention Control Education Intervention on the Psychological Health of Adult Intensive Care Unit Survivors

The goal of this clinical trial is to determine the feasibility and acceptability of a randomized controlled trial comparing a pet dog walking intervention to an attention control education intervention in adult intensive care unit survivors.

The main question[s] it aims to answer are:

• What is the feasibility of a pet dog-walking intervention compared to an attention control education intervention on depression, anxiety, cortisol, and quality of life for adult ICU survivors.
• What is the acceptability of a pet dog-walking intervention compared to an attention control education intervention on depression, anxiety, cortisol, and quality of life for adult ICU survivors.

The secondary question[s] it aims to answer are:

- What are the differences in depression, anxiety, serum cortisol, and quality of life between and within a companion dog walking intervention compared to an attention control education intervention for ICU survivors?

Participants in the intervention group will be asked to:

• Participate in dog walking with their pet dog at least three times per week, for at least 10 minutes each walk, for 8-weeks.
• Wear an activity monitor and record their dog walks in a diary.
• Complete surveys to measure depression, anxiety, and quality of life at the start of the study, after week 4, and after week 8.
• Have blood drawn to measure cortisol levels at the start of the study, after week 4, and after week 8.

Participants in the control group will be asked to:

• Read educational materials about their pet dog's health once every week (education materials are provided by the researchers).
• Wear an activity monitor and record when they read their education materials in a diary.
• Complete surveys to measure depression, anxiety, and quality of life at the start of the study, after week 4, and after week 8.
• Have blood drawn to measure cortisol levels at the start of the study, after week 4, and after week 8.

Participants will be assigned to an intervention group or a control group to see if there are differences in depression, anxiety, serum cortisol, and quality of life.

Study Overview

• Status: Recruiting
• Conditions: Depression; Quality of Life; Anxiety; Post Intensive Care Syndrome
• Intervention / Treatment: Behavioral: Companion Dog Walking; Behavioral: Attention Control Group

• Study Type: Interventional
• Enrollment (Estimated): 30
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Lindsey Nelson, MSN, RN; Phone Number: 719-255-4484; Email: lnr2m@mail.umkc.edu

Study Locations

• United States
  • Colorado
    • Colorado Springs, Colorado, United States, 80907
      • Recruiting
      • Penrose Hospital
    • Colorado Springs, Colorado, United States, 80923
      • Recruiting
      • St. Francis Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Adult (≥18 years)
• ICU survivors (spent ≥24 hours in the ICU)
• Will be discharged directly home from hospital.
• Able to speak, read, and understand English
• Physically capable of dog walking
• Individuals who have symptoms of depression and/or anxiety
• Individuals who own a companion dog and walk their dog <10 minutes/week
• Participants scoring ≤ 20 seconds on the TUG Test

Exclusion Criteria:

• Individuals at high risk for suicide
• Individuals with severe depression or anxiety
• Individuals who recently started treatment for depression and/or anxiety
• Individuals with cognitive impairment
• Dog walking is deemed unsafe with and for the dog
• Medical Provider authorization is indicated but not provided
• Individuals who live outside a 45-mile radius of Colorado Springs.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Other
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Intervention Group; Companion dog walking	Behavioral: Companion Dog Walking; Participants will be asked to walk their dog three times per week, for a minimum of 30 minutes each day of walking, over an 8-week period.
Active Comparator: Attention Control Group; Educational resources about dog health	Behavioral: Attention Control Group; Participants will be asked to read educational materials on dog health once per week, over an 8-week period.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Study Feasibility as assessed by recruitment results, attrition rates, intervention fidelity, and missing data points	Data will be collected to answer the following questions: To what extent does the recruitment procedure produce study participants?; How many participants met inclusion and exclusion criteria?; What are the obstacles to recruitment?; What was the attrition rate of participants?; To what extent was fidelity of the intervention maintained by participants?; To what extent were measurements completed?; What was the extent and patterns of missing data?	Feasibility data will be collected and analyzed from the time identifying, screening, and recruiting eligible participants begins to the time the final participant completes the study; no more than 12 months.
Study Acceptability as assessed by participant responses to survey questions regarding the amount of time spent in the study, the measurement tools used, the masking procedure, and the intervention.	Participants will complete an exit survey and will be asked to report on: (1) the acceptability of the time spent in the study and per session, (2) the acceptability of completing the measurement tools, (3) the acceptability of the masking procedure, (4) the acceptability of the intervention, (5) if they intend to continue the intervention after the end of the study, and (6) to report any suggestions for improvement they have.	Acceptability will be assessed post-intervention after participants complete the 8-week study period.

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in Depression	The Center for Epidemiologic Studies Depression Scale is a 20-item self-report tool that assesses intensity of depression using a 4-point Likert scale. Lower scores indicate milder levels of depression while higher scores indicate more severe depression (potential score 0-60). Clinically meaningful depression is represented by a score of 16 or greater.	Depression will be measured at baseline, half way through the intervention (at the end of week 4), and post intervention (at the end of week 8).
Change in Anxiety	The Spielberger State Trait Anxiety Inventory is a 40-item self-report assessment tool using a 4-point Likert scale that assesses both trait and state anxiety. The higher a participant's score (potential score 20-80 on each subscale) the higher the level of anxiety. No/low anxiety = 20-37 points; moderate anxiety= 38-44 points; and high anxiety=45-80 points, with a cut-off point of 39 indicting clinically significant symptoms of anxiety.	Anxiety will be measured at baseline, half way through the intervention (at the end of week 4), and post intervention (at the end of week 8).
Change in Quality of Life as assessed by health related quality of life indicators including physical functioning, physical and emotional limitations, social functioning, bodily pain, general and mental health.	The Short Form 36 is a 36-item self-report questionnaire using various ranking questions to measure health related quality of life. The Shot Form 36 examines eight dimensions of health related quality of life (physical functioning, physical and emotional limitations, social functioning, bodily pain, general and mental health). The higher the score (max score =100) the better the health and wellbeing, the lower the score (minimum score=0) the poorer the health and wellbeing.	Quality of life will be measured at baseline, half way through the intervention (at the end of week 4), and post intervention (at the end of week 8).
Change in Serum Cortisol	Peripheral venous blood samples will be obtained from participants or analysis at a laboratory.	Serum Cortisol will be measured at baseline, half way through the intervention (at the end of week 4), and post intervention (at the end of week 8).

Collaborators and Investigators

• Sponsor: University of Missouri, Kansas City
• Collaborators: Sigma Theta Tau International Honor Society of Nursing
• Investigators: Principal Investigator: Lindsey Nelson, MSN, RN, University of Missouri, Kansas City

Study record dates

Study Major Dates

• Study Start (Actual): May 15, 2023
• Primary Completion (Estimated): May 1, 2024
• Study Completion (Estimated): May 1, 2024

Study Registration Dates

• First Submitted: March 28, 2023
• First Submitted That Met QC Criteria: April 18, 2023
• First Posted (Actual): April 19, 2023

Study Record Updates

• Last Update Posted (Estimated): December 5, 2023
• Last Update Submitted That Met QC Criteria: November 28, 2023
• Last Verified: April 1, 2023

More Information

Terms related to this study

• Keywords: Depression; Anxiety; Quality of life; Post Intensive Care Syndrome; ICU Survivors; Companion dog
• Additional Relevant MeSH Terms: Behavioral Symptoms; Depression
• Other Study ID Numbers: 2094468

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No