The Effectiveness of Guided Imagery for a Nonprofit's Employees

NCT ID: NCT02191345

Last Updated: 2017-02-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

69 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-07-31

Study Completion Date

2014-11-30

Brief Summary

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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

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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.

Conditions

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Focus of Study Stress

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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10 minute break

Participants asked to take a 10 minute break as usual 3 times per week for 4 weeks

Group Type NO_INTERVENTION

No interventions assigned to this group

Guided Imagery

Participants listen to one of 6 pre-recorded guided imagery tracks 3 times per week for 4 weeks

Group Type EXPERIMENTAL

Guided Imagery

Intervention Type BEHAVIORAL

Guided imagery is a stress management technique that uses verbal suggestion and descriptive language to guide the listener into imagining sensations and visualizing images in the mind in order to bring about a desired physical response, such as reduction in anxiety, stress, or pain. The guided imagery tracks chosen for the study were chosen because their goal is relaxation and stress relief, and their length is under 15 minutes.

Interventions

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Guided Imagery

Guided imagery is a stress management technique that uses verbal suggestion and descriptive language to guide the listener into imagining sensations and visualizing images in the mind in order to bring about a desired physical response, such as reduction in anxiety, stress, or pain. The guided imagery tracks chosen for the study were chosen because their goal is relaxation and stress relief, and their length is under 15 minutes.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institutes of Health (NIH)

NIH

Sponsor Role collaborator

FrontLine Service

OTHER

Sponsor Role lead

Responsible Party

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Kimberly Juhas

Community Research Scholar

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Ashwini Sehgal, MD

Role: STUDY_DIRECTOR

Case Western Reserve University, MetroHealth Medical Center

Kimberly A Juhas, MA

Role: PRINCIPAL_INVESTIGATOR

FrontLine Service

Locations

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FrontLine Service

Cleveland, Ohio, United States

Site Status

Countries

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United States

Other Identifiers

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IRB-2014-743

Identifier Type: OTHER

Identifier Source: secondary_id

MD002265

Identifier Type: -

Identifier Source: org_study_id

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