- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06536387
Storytelling Through Music to Improve Well-being Among Homeless Service Providers
Storytelling Through Music: a Novel Approach to Improve Well-being Among Homeless Service Providers
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Research has found that the burden of secondary traumatic stress among homeless service providers (HSP) is similar to that among other healthcare professionals, including nurses working in urban emergency departments and in inpatient psychiatric hospitals. Left unaddressed, secondary traumatic stress can cause compassion fatigue and emotional exhaustion, furthering a cycle of poor professional quality of life (QoL), burnout, and job turnover. Research has identified that arts-based interventions have promise in helping healthcare professionals cope with work-related emotions, assist in revealing genuine emotions linked to work-related stress, and in improving professional QoL. What remains unclear is if arts-based interventions can yield similar benefits amongst HSPs.
The purpose of this study, therefore, is to evaluate the feasibility of implementing Storytelling Through Music (STM) with HSPs working with the homeless population in Austin, Texas. STM is a six-week intervention that combines storytelling, reflective writing, song-writing, and self-care skills to improve emotion regulation through affective and cognitive coping skills. Our preliminary data suggests STM to be feasible and acceptable, and preliminary evidence demonstrates improved coping, psychosocial well-being, and burnout in nurses. Specifically, this project aims to:
Aim 1: Explore the contextual factors impacting the well-being of frontline HSPs.
Aim 2: Examine the feasibility of implementing Storytelling Through Music with HSPs.
Aim 3: Investigate the preliminary intervention effect on coping (emotion regulation, self-compassion); well-being (anxiety, depressive symptoms, loneliness, post-traumatic growth, insomnia); and work-related factors (secondary traumatic stress, burnout, compassion satisfaction, and intent to leave).
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Texas
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Austin, Texas, United States, 78712
- University of Texas at Austin
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- >18 years old
- employed in a homeless services organization in Austin/Travis County for at least 6 months
- licensed as a nurse or social worker
- ability to read and speak English
- access to computer, internet, and zoom.
Exclusion Criteria:
- previous participation in the STM intervention
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Storytelling Through Music
Storytelling Through Music is a six-week intervention that utilizes storytelling, reflective writing, self-care skills, and song-writing.
The intervention will be administered in small groups of 4-6 participants/group and with a hybrid approach.
The writing workshops will occur online, and the share circle (stories and songs shared with the group) will occur in person.
The group sizes will be kept small to ensure that each participant has adequate time to share their writing during the group sessions.
|
Storytelling Through Music is a six-week intervention that combines storytelling, reflective writing, song-writing, and self-care skills to improve emotion regulation through affective and cognitive coping skills.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Study Feasibility
Time Frame: Immediately post-intervention (6 weeks)
|
Feasibility will be evaluated by tracking the percentage of participants screened and enrolled.
The study will be deemed feasible with a 60% enrollment rate.
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Immediately post-intervention (6 weeks)
|
|
Intervention Feasibility
Time Frame: Immediately post-intervention (6 weeks)
|
Feasibility will be evaluated by tracking the average number of sessions the participants complete.
This intervention will be deemed feasible if 85% of the intervention is completed.
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Immediately post-intervention (6 weeks)
|
|
Intervention Acceptability
Time Frame: Immediately post-intervention (6 weeks)
|
An additional primary endpoint is acceptability.
Acceptability will be evaluated with semi-structured interview questions to understand the participant's perception of intervention delivery and content, as well as the perceived impact.
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Immediately post-intervention (6 weeks)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mean Change from Baseline in Depression Scores at 6 weeks and 10 weeks
Time Frame: Immediately post-intervention and 1-month post-intervention
|
The Patient-Reported Outcomes Measurement Information System (PROMIS) Depression Short-Form 8a will be used.The minimum score is 8, and the maximum score is 40.
Higher scores indicate higher levels of depressive symptoms.
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Immediately post-intervention and 1-month post-intervention
|
|
Mean Change from Baseline in Self-Compassion Scores at 6 weeks and 10 weeks
Time Frame: Immediately post-intervention and 1-month post-intervention
|
Self-Compassion Scale; range is 26-130; higher score is better outcome.
|
Immediately post-intervention and 1-month post-intervention
|
|
Mean Change from Baseline in Anxiety Scores at 6 weeks and 10 weeks
Time Frame: Immediately post-intervention and 1-month post-intervention
|
Patient-Reported Outcomes Measurement Information System (PROMIS) Emotional Distress-Anxiety Short-Form 8a will be used.
The minimum score is 8, and the maximum score is 40.
Higher scores indicate more anxiety.
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Immediately post-intervention and 1-month post-intervention
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Mean Change from Baseline in Emotion Regulation Scores at 6 weeks and 10 weeks
Time Frame: Immediately post-intervention and 1-month post-intervention
|
The Trait Emotional Intelligence Questionnaire-Short Form (TEIQue-SF) will be used to assess trait emotional intelligence (EI).
The questionnaire consists of 30 items rated on a 7-point scale, provides a global trait EI score, and scores for four subscales (i.e., well-being, self-control, emotionality, and sociability).
Higher scores correspond to high levels of trait EI.
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Immediately post-intervention and 1-month post-intervention
|
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Mean Change from Baseline in Loneliness Scores at 6 weeks and 10 weeks
Time Frame: Immediately post-intervention and 1-month post-intervention
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University of California Los Angeles (UCLA) Loneliness Scale; range is 0-60; lower score is better outcome.
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Immediately post-intervention and 1-month post-intervention
|
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Mean Change from Baseline in Post-traumatic Growth Scores at 6 weeks and 10 weeks
Time Frame: Immediately post-intervention and 1-month post-intervention
|
The Post-traumatic Growth Index (PTGI) consists of 21-items that measures the degree of positive changes in an individual's experience after a challenging life event.
The PTGI consists of 5 dimensions: Relating to Others (7-items), New Possibilities (5-items), Personal Strength (4-items), Spiritual Change (2-items), and Appreciation of Life (3-items).
Total scores can range from 0 to 105.
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Immediately post-intervention and 1-month post-intervention
|
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Mean Change from Baseline in Insomnia Scores at 6 weeks and 10 weeks
Time Frame: Immediately post-intervention and 1-month post-intervention
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The Patient-Reported Outcomes Measurement Information System (PROMIS) Sleep Disturbance Short-Form 6a will be used.
The minimum score is 6, and the maximum score is 30.
Higher scores indicate more sleep disturbance.
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Immediately post-intervention and 1-month post-intervention
|
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Mean Change from Baseline in Professional Quality of Life Scores at 6 weeks and 10 weeks
Time Frame: Immediately post-intervention and 1-month post-intervention
|
The Professional Quality of Life (ProQOL) has three subscales: Compassion Satisfaction, Burnout, and Secondary Traumatic Stress.
Scores are reported on individual subscales and can range from 10 to 50.
Higher levels indicate more of the construct.
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Immediately post-intervention and 1-month post-intervention
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Carolyn Phillips, University of Texas at Austin
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- STUDY00006156
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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