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Clinical Trials/NCT02191345
NCT02191345CompletedNot Applicable

A Randomized Controlled Trial Measuring the Effectiveness of Prerecorded Guided Imagery in Reducing Compassion Fatigue, Burnout, Perceived Stress, and State Anxiety of a Mental Health Nonprofit's Employees

FrontLine Service2 sites in 1 country69 target enrollmentStarted: July 1, 2014Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
69
Locations
2
Primary Endpoint
State Anxiety as Measured by the State Anxiety Short Form

Study Overview

Brief Summary

Primary Aim A. To determine if listening to prerecorded guided imagery 3 times per week for 4 weeks will reduce state anxiety, perceived stress, burnout, compassion fatigue, and vicarious trauma in Fronltine Service staff.

Primary Aim B. To determine if staff will continue to listen to guided imagery after the first 4 weeks of the study is over.

Detailed Description

The purpose of this study is to compare the change in stress levels of employees who listen to prerecorded guided imagery to employees who take breaks, and to determine if employees are likely to adopt prerecorded guided imagery as a self-care tool.

Participants will be randomly assigned to either the guided imagery group or the control group. Members of the control group will be asked to take a 10 minute break 3 times per week for 4 weeks. Members of the guided imagery group will be asked to listen to one prerecorded guided imagery track 3 times per week for 4 weeks. All participants will fill out questionnaires before and after the 4 week period. All participants will fill out a short form before and after listening to each guided imagery, or before and after taking each break.

Phase 2: After phase 1 is complete, all participants will have the option to participate in phase 2 of the study. During phase 2, participants will receive a calendar and put a mark on every day that they listen to a guided imagery track. At the end of 4 weeks, participants will turn in the calendar.

Study Design

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

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Staff of a nonprofit who work a minimum of three shifts per week
  • Willing and able to use about 8-15 minutes of their lunch hours three times per week for for four weeks for the study

Exclusion Criteria

  • Staff members will be excluded from the study if they currently listen to guided imagery
  • Those currently experiencing drug or alcohol abuse, suicidal ideation, or other serious mental health issue while not under the care of a trained mental health professional will also be excluded

Outcomes

Primary Outcomes

State Anxiety as Measured by the State Anxiety Short Form

Time Frame: 4 weeks

Participants in the experimental group will fill out the State Anxiety Short Form, a 6-item questionnaire before and after listening to guided imagery. Participants in the control group will fill out the same measure before and after taking a break. This will be done 3 times per week for a duration of 4 weeks.

Secondary Outcomes

  • Perceived Stress as measured by the Perceived Stress Scale(4 weeks)
  • Compassion Fatigue, Compassion Satisfaction, and Burnout, as measured by the ProQol(4 weeks)

Investigators

Sponsor
FrontLine Service
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Kimberly Juhas

Community Research Scholar

FrontLine Service

Study Sites (2)

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