The Effects of the Safe and Sound Protocol on PTSD Symptoms and Anxiety
Primary Purpose
Post Traumatic Stress Disorder, Anxiety
Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Safe and Sound Protocol
Psychotherapy
Sponsored by
About this trial
This is an interventional treatment trial for Post Traumatic Stress Disorder focused on measuring Post Traumatic Stress Disorder, Anxiety, PTSD treatment, Safe and Sound Protocol, SSP, auditory intervention, music intervention
Eligibility Criteria
SSP Intervention Arm:
Inclusion Criteria:
- Client at Spencer Psychology in Bloomington, Indiana
- Diagnosed with PTSD or trauma not otherwise specified
- Already have agreed with therapist to administer SSP as a part of therapy
Exclusion Criteria:
- Tinnitus or hearing loss
- Diagnosed with cardiac arrhythmia
- At high risk for 2019 novel coronavirus (COVID-19) complications based on Center for Disease Control (CDC) guidelines, unless vaccinated
Comparison (Treatment As Usual) Arm Additional Criteria:
Inclusion Criteria:
- 18 years of age or older
- Active psychotherapy client at Spencer Psychology
- Diagnosis of PTSD or trauma not otherwise specified
- Match range of PCL-5 baseline scores with treatment arm during screener survey
Exclusion criteria:
- Currently using or have previously used the Safe and Sound Protocol (SSP) in therapy
- Current therapy includes Eye Movement Desensitization and Reprocessing (EMDR)
Sites / Locations
- Spencer Psychology
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Psychotherapy + SSP
Psychotherapy (treatment as usual)
Arm Description
All subjects enrolled in this study will receive the SSP intervention
Subjects who are receiving psychotherapy but not the SSP intervention
Outcomes
Primary Outcome Measures
Post Traumatic Stress Disorder Symptoms
Post Traumatic Stress Disorder Checklist for the DSM-5 (PCL-5), a 20-item self report, will be used. Total symptom severity scores range from 0 to 80, with higher scores indicating higher symptomology (poorer outcome).
Anxiety
Generalized Anxiety Disorder scale (GAD-7), 7-item self report will be used. Scores range from 0-21 points, with higher scores indicating greater anxiety symptoms (poorer outcome).
Secondary Outcome Measures
Self-reported disruption of autonomic reactivity
Body Perception Questionnaire (BPQ), 20-item self-report, be used. Raw scores range from 0-100, with higher scores indicating greater level of symptoms associated with autonomic activity (poorer outcome).
Mean heart period during posture shifts [SSP arm only]
Mean heart period during supine, sitting, and standing posture shifts will be measured using an earlobe pulse sensor (Photoplethysmography). Longer heart period (higher values, reported in milliseconds) are indicative of lower autonomic arousal states. This metric is intended as a measure of mechanism and and high values may be associated with a better outcome.
Respiratory sinus arrhythmia (RSA) during posture shifts [SSP arm only]
Respiratory sinus arrhythmia (RSA) - a component of heart rate variability - will be measured during supine, sitting, and standing posture shifts using an earlobe pulse sensor (Photoplethysmography). Greater RSA (higher values, reported in ln[milliseconds]^2) is associated with greater parasympathetic activity, which can help reduce physiological threat responses. This metric is intended to measure mechanism and high values may be associated with a better outcome.
Full Information
NCT ID
NCT04999852
First Posted
August 2, 2021
Last Updated
June 13, 2023
Sponsor
Indiana University
Collaborators
Spencer Psychology
1. Study Identification
Unique Protocol Identification Number
NCT04999852
Brief Title
The Effects of the Safe and Sound Protocol on PTSD Symptoms and Anxiety
Official Title
The Effects of the Safe and Sound Protocol on PTSD Symptoms and Anxiety
Study Type
Interventional
2. Study Status
Record Verification Date
June 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 12, 2021 (Actual)
Primary Completion Date
September 30, 2023 (Anticipated)
Study Completion Date
September 30, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Indiana University
Collaborators
Spencer Psychology
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The Safe and Sound Protocol (SSP) is a passive acoustic intervention that is designed as a "neural exercise" to promote efficient regulation of autonomic state. Prior research has shown that the SSP can improve autonomic function, auditory hypersensitivities, and emotion regulation in individuals with Autism Spectrum Disorders. This observational pilot study is being conducted to establish methods for an upcoming randomized controlled trial to test the utility of the SSP for trauma treatment.
This study will enroll clients at the Spencer Psychology clinic who are set to take part in SSP under the supervision of their therapist. Because the therapists have participated in the design of the protocol and will participate in data collection and analysis, SSP will be considered a research procedure. In addition to taking part in SSP, subjects complete a set of questionnaires and have their pulse measured before starting the SSP intervention, after having completed 2/5 hours of the SSP, one week after completing all 5 hours of the SSP, and one month after completing the SSP intervention. The investigators will also pull relevant information from Spencer Psychology's medical records to document diagnosis, track client progress during study, and augment self-reported demographics. Clients who are receiving psychotherapy but not the SSP will be recruited as a comparison group.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post Traumatic Stress Disorder, Anxiety
Keywords
Post Traumatic Stress Disorder, Anxiety, PTSD treatment, Safe and Sound Protocol, SSP, auditory intervention, music intervention
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
46 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Psychotherapy + SSP
Arm Type
Experimental
Arm Description
All subjects enrolled in this study will receive the SSP intervention
Arm Title
Psychotherapy (treatment as usual)
Arm Type
Active Comparator
Arm Description
Subjects who are receiving psychotherapy but not the SSP intervention
Intervention Type
Device
Intervention Name(s)
Safe and Sound Protocol
Other Intervention Name(s)
SSP
Intervention Description
SSP is a non-invasive acoustic vagus nerve stimulator consisting of 5 hours of filtered and processed music designed to promote efficient regulation of autonomic state, and available through an app. The SSP is delivered via a mobile app and may fall under the heading of medical devices under the category of software functions/mobile medical applications.
Intervention Type
Behavioral
Intervention Name(s)
Psychotherapy
Intervention Description
All participants, regardless of study arm, will be recruited from the pool of Spencer Psychology clients who are actively recieving psychotherapy. Participants will continue to recieve psychotherapy during the course of the study.
Primary Outcome Measure Information:
Title
Post Traumatic Stress Disorder Symptoms
Description
Post Traumatic Stress Disorder Checklist for the DSM-5 (PCL-5), a 20-item self report, will be used. Total symptom severity scores range from 0 to 80, with higher scores indicating higher symptomology (poorer outcome).
Time Frame
2--4 months
Title
Anxiety
Description
Generalized Anxiety Disorder scale (GAD-7), 7-item self report will be used. Scores range from 0-21 points, with higher scores indicating greater anxiety symptoms (poorer outcome).
Time Frame
2--4 months
Secondary Outcome Measure Information:
Title
Self-reported disruption of autonomic reactivity
Description
Body Perception Questionnaire (BPQ), 20-item self-report, be used. Raw scores range from 0-100, with higher scores indicating greater level of symptoms associated with autonomic activity (poorer outcome).
Time Frame
2--4 months
Title
Mean heart period during posture shifts [SSP arm only]
Description
Mean heart period during supine, sitting, and standing posture shifts will be measured using an earlobe pulse sensor (Photoplethysmography). Longer heart period (higher values, reported in milliseconds) are indicative of lower autonomic arousal states. This metric is intended as a measure of mechanism and and high values may be associated with a better outcome.
Time Frame
2--4 months
Title
Respiratory sinus arrhythmia (RSA) during posture shifts [SSP arm only]
Description
Respiratory sinus arrhythmia (RSA) - a component of heart rate variability - will be measured during supine, sitting, and standing posture shifts using an earlobe pulse sensor (Photoplethysmography). Greater RSA (higher values, reported in ln[milliseconds]^2) is associated with greater parasympathetic activity, which can help reduce physiological threat responses. This metric is intended to measure mechanism and high values may be associated with a better outcome.
Time Frame
2--4 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
SSP Intervention Arm:
Inclusion Criteria:
Client at Spencer Psychology in Bloomington, Indiana
Diagnosed with PTSD or trauma not otherwise specified
Already have agreed with therapist to administer SSP as a part of therapy
Exclusion Criteria:
Tinnitus or hearing loss
Diagnosed with cardiac arrhythmia
At high risk for 2019 novel coronavirus (COVID-19) complications based on Center for Disease Control (CDC) guidelines, unless vaccinated
Comparison (Treatment As Usual) Arm Additional Criteria:
Inclusion Criteria:
18 years of age or older
Active psychotherapy client at Spencer Psychology
Diagnosis of PTSD or trauma not otherwise specified
Match range of PCL-5 baseline scores with treatment arm during screener survey
Exclusion criteria:
Currently using or have previously used the Safe and Sound Protocol (SSP) in therapy
Current therapy includes Eye Movement Desensitization and Reprocessing (EMDR)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jacek Kolacz, PhD
Organizational Affiliation
Indiana University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Spencer Psychology
City
Bloomington
State/Province
Indiana
ZIP/Postal Code
47403
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
The Effects of the Safe and Sound Protocol on PTSD Symptoms and Anxiety
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