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Home-based SSP on Individuals With PWS

Primary Purpose

Prader-Willi Syndrome

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Safe and Sound Protocol
Sponsored by
Indiana University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Prader-Willi Syndrome focused on measuring Polyvagal Theory, Social Behavior, Hyperacusis, Prosody, Auditory intervention

Eligibility Criteria

3 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Child participants must meet criteria for Prader-Willi Syndrome (per parent membership in Prader-Willi Parent Support Group).
  2. Child participants must be between ages 3-17 years. Parent must be 18 years or older.
  3. Child participants must have normal hearing (confirmed via parental report on Qualtrics questionnaire)

Exclusion Criteria:

1) Child participants who are hearing-impaired (without correction)

Sites / Locations

  • Integrated Listening Systems

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Safe and Sound Protocol

Arm Description

All child participants will participate in 1 pre-intervention assessment and 1 post-intervention assessment. The auditory intervention (i.e., Safe and Sound Protocol, SSP) will last for 1 hour per day, for 5 consecutive days.

Outcomes

Primary Outcome Measures

Change from baseline in sensory sensitivities at 1 week
Brain-Body Center Sensory Scales (BBC Sensory Scales) (parental questionnaire)

Secondary Outcome Measures

Change from baseline in disruptive behavior at 1 week
Developmental Behavior Checklist (DBC2) (questionnaire)
Change from baseline in social behavior at 1 week
Safe and Sound Protocol (SSP) Parent Questionnaire
Change from baseline in Foundational Abilities (balance, gross & fine motor control, sensory, social/emotional, auditory/language and attention/organization and sleep) at 1 week
Measure of Foundational Abilities (MFA) questionnaire
Change from baseline in prosody at 1 week
Prosody assessment of recorded speech

Full Information

First Posted
February 25, 2019
Last Updated
February 18, 2022
Sponsor
Indiana University
Collaborators
Integrated Listening Systems
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1. Study Identification

Unique Protocol Identification Number
NCT03871751
Brief Title
Home-based SSP on Individuals With PWS
Official Title
Evaluating the Effectiveness of Home-based SSP on Individuals With PWS
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Terminated
Why Stopped
Insufficient resources to complete study as planned
Study Start Date
April 8, 2019 (Actual)
Primary Completion Date
December 16, 2019 (Actual)
Study Completion Date
December 16, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Indiana University
Collaborators
Integrated Listening Systems

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The Polyvagal Theory focuses on how function and structure changed in the vertebrate autonomic nervous system during evolution. The theory is named for the vagus, a major cranial nerve that regulates bodily state. As a function of evolution, humans and other mammals have a "new" vagal pathway that links the regulation of bodily state to the control of the muscles of the face and head including the middle ear muscles. These pathways regulating body state, facial gesture, listening (i.e., middle ear muscles), and vocal communication collectively function as a Social Engagement System (SES). Because the Social Engagement System is an integrated system, interventions influencing one component of this system (e.g., middle ear muscles) may impact on the other components. Individuals with Prader-Willi Syndrome (PWS) exhibit many behaviors that are consistent with a compromised Social Engagement System. Atypical function of the Social Engagement System results in problems associated with state regulation (e.g., impulsivity, tantrums, and difficulty with change in routine), ingestion (e.g., difficulties in sucking at birth, hyperphagia), coordination of suck/swallow/breathe, intonation of vocalizations, auditory processing and hypersensitivity, and socialization. The investigatiors propose to confirm that several features of the behavioral phenotype of PWS may be explained within the context of a dysfunctional SES, which may be partially rehabilitated via an intervention designed as a 'neural exercise' of the SES (i.e., the Safe and Sound Protocol, "SSP"). Specific Aims: Aim I: To demonstrate the effectiveness of the Safe and Sound Protocol (SSP) on improvement of social and regulation behaviors in individuals with PWS. Aim II: To evaluate a new methodology for collecting and evaluating vocal samples for analyses of prosody, one of the indices of the functioning of the SES.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prader-Willi Syndrome
Keywords
Polyvagal Theory, Social Behavior, Hyperacusis, Prosody, Auditory intervention

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
All participants will receive the auditory intervention.
Masking
None (Open Label)
Masking Description
No masking.
Allocation
N/A
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Safe and Sound Protocol
Arm Type
Experimental
Arm Description
All child participants will participate in 1 pre-intervention assessment and 1 post-intervention assessment. The auditory intervention (i.e., Safe and Sound Protocol, SSP) will last for 1 hour per day, for 5 consecutive days.
Intervention Type
Behavioral
Intervention Name(s)
Safe and Sound Protocol
Other Intervention Name(s)
Listening Project Protocol
Intervention Description
The auditory intervention will consist of listening to computer-altered acoustic stimulation, designed to modulate the frequency band of vocal music passed to the participant. The frequency characteristics of the acoustic stimulation are selected to emphasize the relative importance of specific frequencies in conveying the information embedded in human speech. Modulation of the acoustic energy within the frequencies of human voice, similar to an exaggerated vocal prosody, are hypothesized to recruit and modulate the neural regulation of the middle ear muscles and to functionally reduce sound hypersensitivities and improve auditory processing.
Primary Outcome Measure Information:
Title
Change from baseline in sensory sensitivities at 1 week
Description
Brain-Body Center Sensory Scales (BBC Sensory Scales) (parental questionnaire)
Time Frame
pre-intervention (within 1 week before intervention), post-intervention (within 1 week after intervention)
Secondary Outcome Measure Information:
Title
Change from baseline in disruptive behavior at 1 week
Description
Developmental Behavior Checklist (DBC2) (questionnaire)
Time Frame
pre-intervention (within 1 week before intervention), post-intervention (within 1 week after intervention)
Title
Change from baseline in social behavior at 1 week
Description
Safe and Sound Protocol (SSP) Parent Questionnaire
Time Frame
post-intervention (within 1 week after intervention)
Title
Change from baseline in Foundational Abilities (balance, gross & fine motor control, sensory, social/emotional, auditory/language and attention/organization and sleep) at 1 week
Description
Measure of Foundational Abilities (MFA) questionnaire
Time Frame
pre-intervention (within 1 week before intervention), post-intervention (within 1 week after intervention)
Title
Change from baseline in prosody at 1 week
Description
Prosody assessment of recorded speech
Time Frame
pre-intervention (within 1 week before intervention), post-intervention (within 1 week after intervention)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Child participants must meet criteria for Prader-Willi Syndrome (per parent membership in Prader-Willi Parent Support Group). Child participants must be between ages 3-17 years. Parent must be 18 years or older. Child participants must have normal hearing (confirmed via parental report on Qualtrics questionnaire) Exclusion Criteria: 1) Child participants who are hearing-impaired (without correction)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jacek Kolacz, PhD
Organizational Affiliation
Indiana University/Kinsey Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Integrated Listening Systems
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80014
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
11587772
Citation
Porges SW. The polyvagal theory: phylogenetic substrates of a social nervous system. Int J Psychophysiol. 2001 Oct;42(2):123-46. doi: 10.1016/s0167-8760(01)00162-3.
Results Reference
background
PubMed Identifier
25136545
Citation
Porges SW, Bazhenova OV, Bal E, Carlson N, Sorokin Y, Heilman KJ, Cook EH, Lewis GF. Reducing auditory hypersensitivities in autistic spectrum disorder: preliminary findings evaluating the listening project protocol. Front Pediatr. 2014 Aug 1;2:80. doi: 10.3389/fped.2014.00080. eCollection 2014.
Results Reference
background

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Home-based SSP on Individuals With PWS

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