NCT03530943

Brief Summary

The current study utilized a randomized controlled trial, conducted in a real-life setting, to determine whether, how, under which conditions, and for whom, infusing various levels of human-animal interaction (HAI) in a 4-week, university-based stress prevention program provides an effective approach to prevent negative ramifications of university students stress, promote student executive functioning and learning, while safeguarding animal welfare. This study will examine effects of sole exposure to evidence-based stress prevention content, hands-on HAI with registered PET Partner teams, or combinations thereof on students' moment-to-moment well-being and longer-term functioning in socioemotional, cognitive and physiological domains.This study will also develop a comprehensive coding system and measure the dynamic nature of behavior of participants, handlers and animals during university- based animal assisted activities, as well as the HAI environment. The data and analyses will then be utilized to inform the development of a quantitative measure to capture of the quality of human animal interaction in various settings to experimentally determine causal pathways underlying program effects on humans and animals.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
300

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Aug 2016

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2016

Completed
1.6 years until next milestone

First Submitted

Initial submission to the registry

March 20, 2018

Completed
2 months until next milestone

First Posted

Study publicly available on registry

May 21, 2018

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2018

Completed
Last Updated

May 21, 2018

Status Verified

May 1, 2018

Enrollment Period

2.3 years

First QC Date

March 20, 2018

Last Update Submit

May 8, 2018

Conditions

Outcome Measures

Primary Outcomes (9)

  • Change in Salivary Cortisol (Diurnal)

    Participants provided three samples (wakeup, afternoon, bedtime) over two consecutive days for a total of six samples.

    Diurnal salivary cortisol was measured three times: at baseline one week before the intervention; at post-test one week following the conclusion of the intervention (baseline+5 weeks); and at follow-up six weeks after the posttest (baseline+11 weeks).

  • Change in Salivary Cortisol (Basal)

    Salivary cortisol was measured immediately preceding the beginning of each of the four programming sessions

  • Change in Salivary Cortisol (Momentary Reactivity)

    Salivary cortisol was measured two to three times each of the four programming sessions in response to various program activities.

  • Change in Momentary Emotion (Experience Sampling Method Questionnaire)

    Momentary emotion was measured three times each of the four programming sessions, immediately before entering the program area, and two additional times 30 and 50 minutes after the program start following various 10 minute activities

  • Change in Learning and Study Strategies (Learning and Study Strategies Inventory)

    Learning and study strategies were measured three times: at baseline one week before the intervention; at post-test one week following the conclusion of the intervention (baseline+5 weeks); at follow-up six weeks after the posttest (baseline+11 weeks).

  • Change in Depression (Beck Depression Inventory)

    Depression was measured three times: at baseline one week before the intervention; at post-test one week following the conclusion of the intervention (baseline + 5 weeks); and at follow-up six weeks after the posttest (baseline + 11 weeks).

  • Change in Anxiety (Beck Anxiety Inventory)

    Anxiety was measured three times: at baseline one week before the intervention; at post-test one week following the conclusion of the intervention (baseline + 5 weeks); and at follow-up six weeks after the posttest (baseline + 11 weeks).

  • Change in Perceived Stress (Perceived Stress Scale - 10)

    The Perceived Stress Scale -10 is a 10-item measure resulting in a single composite score ranging from 0 to 40 with higher scores representing higher levels of reported perceived stress.

    Perceived stress was measured three times: at baseline one week before the intervention; at post-test one week following the conclusion of the intervention (baseline + 5 weeks); and at follow-up six weeks after the posttest (baseline + 11 weeks).

  • Change in Executive Functioning (Behavior Rating Inventory of Executive Functioning - Adult Version)

    Executive functioning was measured three times: at baseline one week before the intervention; at post-test one week following the conclusion of the intervention (baseline + 5 weeks); and at follow-up six weeks after the posttest (baseline + 11 weeks).

Secondary Outcomes (5)

  • Salivary Alpha-Amylase (Diurnal)

    Diurnal salivary alpha-amylase was measured three times: at baseline one week before the intervention; at post-test one week following the conclusion of the intervention (baseline+5 weeks); and at followup six weeks after the posttest (baseline+11 weeks)

  • Salivary Alpha-Amylase (Basal)

    Salivary alpha-amylase was measured immediately preceding the beginning of each of the four programming sessions

  • Salivary Alpha-Amylase (Momentary Reactivity)

    Salivary alpha-amylase was measured two to three times during each of the four programming sessions in response to various program activities.

  • Attitudes Towards Learning

    Attitudes towards learning were measured three times: at baseline one week before the intervention; at post-test one week following the conclusion of the intervention (baseline+5 weeks); and at follow-up six weeks after the posttest (baseline+11 weeks)

  • Self-perceived worry (Penn State Worry Questionnaire)

    Self-perceived worry was measured three times: at baseline one week before the intervention; at post-test one week following the conclusion of the intervention (baseline + 5 weeks); and at follow-up six weeks after the posttest (baseline + 11 weeks).

Other Outcomes (1)

  • Video observation coding

    Recordings captured each dog-handler station, capturing 70-80 minutes throughout the program beginning 10 minutes before participants entry in the room through the end of each session.

Study Arms (3)

Academic Stress Management

ACTIVE COMPARATOR

Students assigned to the Academic Stress Management (ASM) condition will attend a series of once weekly, one hour long workshops over four consecutive weeks during which time they will receive 100% exposure to various evidence-based academic stress management tools.

Behavioral: Academic Stress Management tools

Human Animal Interaction Enhanced

EXPERIMENTAL

Students assigned to the Human Animal Interaction - Enhanced (HAI-E) condition will attend a series of once weekly, one hour long workshops over four consecutive weeks. This group receives 50% exposure to structured and unstructured animal assisted activities and 50% exposure to various evidence-based academic stress management tools.

Behavioral: Animal Assisted ActivitiesBehavioral: Academic Stress Management tools

Human Animal Interaction only

EXPERIMENTAL

Students assigned to the Human Animal Interaction - only (HAI-O) condition will attend a series of once weekly, one hour long workshops over four consecutive weeks. This group will be receive 100% exposure to structured and semi-structured animal assisted activities.

Behavioral: Animal Assisted Activities

Interventions

Students interact with canines in small group settings under the supervision of their handlers during structured and semi-structured activities designed to strengthen physiological, emotion and behavioral regulation

Human Animal Interaction EnhancedHuman Animal Interaction only

Evidence-based workshops focus on evidence-based content and activities designed to enhance academic stress management knowledge and skills, motivation and learning, adaptive sleep, and study and test-taking behavior through strengthening physiological, emotion and behavioral regulation

Academic Stress ManagementHuman Animal Interaction Enhanced

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Current enrollment at the campus

You may not qualify if:

  • Children under 18 years old
  • Prior history of animal abuse
  • Participation in an an academic stress management workshop within 6 months of study participation

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Washington State University

Pullman, Washington, 99164, United States

RECRUITING

Related Publications (2)

  • Pendry P, Carr AM, Gee NR, Vandagriff JL. Randomized Trial Examining Effects of Animal Assisted Intervention and Stress Related Symptoms on College Students' Learning and Study Skills. Int J Environ Res Public Health. 2020 Mar 15;17(6):1909. doi: 10.3390/ijerph17061909.

  • Pendry P, Kuzara S, Gee NR. Evaluation of Undergraduate Students' Responsiveness to a 4-Week University-Based Animal-Assisted Stress Prevention Program. Int J Environ Res Public Health. 2019 Sep 10;16(18):3331. doi: 10.3390/ijerph16183331.

MeSH Terms

Conditions

Anxiety DisordersBehavior, Animal

Condition Hierarchy (Ancestors)

Mental DisordersBehavior

Study Officials

  • Patricia Pendry, PhD

    Washington State University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Patricia Pendry, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Masking Details
Participants remained unaware of their treatment allocation until after completing the baseline (pretest) assessments and the onset of their intervention
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 20, 2018

First Posted

May 21, 2018

Study Start

August 1, 2016

Primary Completion

December 1, 2018

Study Completion

December 1, 2018

Last Updated

May 21, 2018

Record last verified: 2018-05

Data Sharing

IPD Sharing
Will not share

Locations