- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03849144
The Effect of a Therapy Dog Activity on Employees' Stress, Mood, and Job Satisfaction and Commitment
October 11, 2024 updated by: Virginia Commonwealth University
The goal of the current study is to determine if participating in a therapy dog activity is associated with changes in perceived stress, mood, and job satisfaction and commitment.
A secondary goal is to explore a potential dose effect of multiple treatments as well as control for novelty effect.
Study Overview
Status
Withdrawn
Conditions
Intervention / Treatment
Detailed Description
This study will be conducted at Aetna Headquarters in Hartford, Connecticut.
A pre-post repeated measures design will be used to compare study participant outcomes between a treatment (therapy dog activity) and comparison (low impact physical activity) condition.
Outcome variables of interest are perceived stress measured by a stress visual analog scale (SVAS), mood measured by the Positive and Negative Affect Scale (PANAS), and job satisfaction and commitment measured by an investigator-developed Job Satisfaction Survey (consisting of a combination of existing validated scales).
Pet ownership, attitudes toward dogs measured by the Dog Attitude Scale, and trait stress, measured by the Perceived Stress Scale, will be assessed as moderating variables.
Study Type
Interventional
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Connecticut
-
Hartford, Connecticut, United States, 06156
- Aetna Headquarters
-
-
Virginia
-
Richmond, Virginia, United States, 23298
- Virginia Commonwealth University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Current Aetna employees
Exclusion Criteria:
- Individuals not employed by Aetna. Note:employees are self-selecting to participate, therefore dog fears or allergies are not listed as exclusion criteria.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Therapy dog activity
Interact with visiting therapy dogs for 15 minutes on two Fridays
|
Visiting therapy dogs and their owners, evaluated and registered as therapy dog teams with Pet Partners will be spread around a large room on the Aetna campus.
Employees will arrive at scheduled times to visit with the dogs for 15 minutes, talking to the dogs and owners and petting the dogs
|
|
Active Comparator: Low impact physical activity
Participate in 15-minute low impact physical activity on two Fridays
|
The low impact exercise will consist of stretching exercises conducted by a member of Aetna's wellness team in the same room for 15 minutes.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Single Item Stress Measure
Time Frame: Baseline to week 3
|
Changes in self reported stress on visual analog scale (VAS) immediately before and after each activity.
Scale ranges from "none" to "most severe imaginable" on 15 cm scale.
|
Baseline to week 3
|
|
20-item Positive and Negative Affect Schedule
Time Frame: Baseline to week 3
|
Self reported mood immediately before and after each activity.
Each item is scored 1-5 (1 = strongly disagree; 5 = strongly agree).
10 items comprise the positive affect scale with scores ranging from 10 - 50, with higher scores indicating higher positive affect.
10 items comprise the negative affect scale with total scores ranging from 10 - 50, with lower scores indicating lower negative affect.
|
Baseline to week 3
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Single Item Stress Measure
Time Frame: Baseline to week 5
|
Changes in self reported stress on visual analog scale (VAS) after two intervention activities.
Scale ranges from "none" to "most severe imaginable" on 15 cm scale.
|
Baseline to week 5
|
|
20-item Positive and Negative Affect Schedule
Time Frame: Baseline to week 5
|
Self reported mood two intervention activities.
Each item is scored 1-5 (1 = strongly disagree; 5 = strongly agree).
10 items comprise the positive affect scale with scores ranging from 10 - 50, with higher scores indicating higher positive affect.
10 items comprise the negative affect scale with total scores ranging from 10 - 50, with lower scores indicating lower negative affect.
|
Baseline to week 5
|
|
9-item Job Satisfaction and Commitment Scale
Time Frame: Baseline to week 5
|
Self reported job satisfaction ( 3 items) and commitment (6 items) at baseline, after the first and last activity.
Each item is scored 1-5 (1 = strongly disagree, 5 = strongly agree).
Total scores range from 9-45 with higher scores indicating greater job satisfaction and commitment
|
Baseline to week 5
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Sandra Barker, PhD, Virginia Commonwealth University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
March 15, 2019
Primary Completion (Estimated)
May 10, 2019
Study Completion (Estimated)
July 12, 2019
Study Registration Dates
First Submitted
November 21, 2018
First Submitted That Met QC Criteria
February 19, 2019
First Posted (Actual)
February 21, 2019
Study Record Updates
Last Update Posted (Actual)
October 15, 2024
Last Update Submitted That Met QC Criteria
October 11, 2024
Last Verified
October 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- HM20014106
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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