Optimizing the Social Engagement System in Prader-Willi Syndrome: Insights From the Polyvagal Theory

March 30, 2023 updated by: Stephen Porges, Indiana University

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. We propose to confirm that several features of the behavioral phenotype of PWS may be explained within the context of a dysfunctional SES (Specific Aim I), which may be partially rehabilitated via an intervention designed as a 'neural exercise' of the SES (Specific Aim II).

Specific Aims:

Aim I: To demonstrate that children with PWS have atypical regulation of the SES. We hypothesize these effects will be manifested by dampened vagal regulation of the heart (low parasympathetic tone); poor middle ear muscle regulation resulting in auditory hypersensitivities and poor auditory processing; lack of voice intonation (prosody), and difficulties in accurately detecting the emotions of others.

Aim II: To demonstrate the effectiveness of the Listening Project Protocol (LPP) in decreasing the atypical features of the SES in adolescents with PWS. We hypothesize that individuals who complete the LPP will have improved vagal regulation of the heart, improved middle ear muscle regulation, increased voice intonation and improved ability to accurately detect the emotions of others.

Study Overview

Status

Terminated

Study Type

Interventional

Enrollment (Actual)

5

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Massachusetts
      • Brewster, Massachusetts, United States, 02631
        • Latham Centers School

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

13 years to 25 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Participants must be current residents at Latham Centers (LC) School in Brewster MA
  2. Participants must meet criteria for Prader-Willi Syndrome
  3. Participants must be between ages 13 - 25 years
  4. Participants must have normal hearing
  5. Participants must have normal vision (or corrected vision)

Exclusion Criteria:

  1. Individuals with current (or a history of) heart disease
  2. Individuals who are hearing-impaired
  3. Individuals who are being treated for seizure disorder
  4. Individuals who do not read/speak English
  5. Individuals who are sight-impaired without correction

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Filtered Music Intervention
All participants will participate in pre-intervention assessments (6 months, 1 week prior) and post-intervention assessments (1 week, 1 month post). The Filtered Music Intervention (i.e., Listening Project Protocol) will last for 1 hour per day, for 5 consecutive days.
The filtered music 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.
Other Names:
  • Safe and Sound Protocol

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Effect of Intervention on Autonomic regulation
Time Frame: Change from 1 week pre-intervention RSA to 1 month post-intervention
Respiratory sinus arrhythmia (RSA)
Change from 1 week pre-intervention RSA to 1 month post-intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Effect of Intervention on Heart period
Time Frame: Change from 1 week pre-intervention heart period to 1 month post-intervention
heart period
Change from 1 week pre-intervention heart period to 1 month post-intervention
Effect of Intervention on Auditory processing
Time Frame: Change from 1 week pre-intervention Filtered Words to 1 month post-intervention
Filtered Words subtest of SCAN
Change from 1 week pre-intervention Filtered Words to 1 month post-intervention
Effect of Intervention on Auditory processing
Time Frame: Change from 1 week pre-intervention Competing Words to 1 month post-intervention
Competing Words subtest of SCAN
Change from 1 week pre-intervention Competing Words to 1 month post-intervention
Effect of Intervention on Sensory Sensitivities
Time Frame: Change from 1 week pre-intervention BBC Sensory Scales to 1 month post-intervention
BBC Sensory Scales (questionnaire)
Change from 1 week pre-intervention BBC Sensory Scales to 1 month post-intervention
Effect of Intervention on Latency to Affect recognition
Time Frame: Change from 1 week pre-intervention DARE (latency) to 1 month post-intervention
Dynamic Affect Recognition Evaluation (DARE) - latency
Change from 1 week pre-intervention DARE (latency) to 1 month post-intervention
Effect of Intervention on Accuracy of Affect recognition
Time Frame: Change from 1 week pre-intervention DARE (accuracy) to 1 month post-intervention
Dynamic Affect Recognition Evaluation (DARE) - accuracy
Change from 1 week pre-intervention DARE (accuracy) to 1 month post-intervention
Effect of Intervention on Prosody
Time Frame: Change from 1 week pre-intervention Prosody to 1 month post-intervention
Analyses of vocal recordings
Change from 1 week pre-intervention Prosody to 1 month post-intervention
Effect of Intervention on Disruptive Behavior
Time Frame: Change from 1 week pre-intervention DBC to 1 month post-intervention
Developmental Behavior Checklist (DBC) (questionnaire)
Change from 1 week pre-intervention DBC to 1 month post-intervention
Effect of Intervention on Social behavior
Time Frame: Change from 1 week post-intervention LPP to 1 month post-intervention
Listening Project Parent (LPP) Questionnaire
Change from 1 week post-intervention LPP to 1 month post-intervention
Effect of Intervention on Oxytocin
Time Frame: Change from 1 week pre-intervention oxytocin to 1 month post-intervention
oxytocin levels derived from salivary sample
Change from 1 week pre-intervention oxytocin to 1 month post-intervention
Effect of Intervention on Vasopressin
Time Frame: Change from 1 week pre-intervention vasopressin to 1 month post-intervention
vasopressin levels derived from salivary sample
Change from 1 week pre-intervention vasopressin to 1 month post-intervention

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Stability of Autonomic regulation
Time Frame: Change from 6 months pre-intervention RSA to 1 week pre-intervention
Respiratory sinus arrhythmia (RSA)
Change from 6 months pre-intervention RSA to 1 week pre-intervention
Immediate effects of intervention on Autonomic regulation
Time Frame: Change from 1 week pre-intervention RSA to 1 week post-intervention
Respiratory sinus arrhythmia (RSA)
Change from 1 week pre-intervention RSA to 1 week post-intervention
Short-term effects of intervention on Autonomic regulation
Time Frame: Change from 1 week post-intervention RSA to 1 month post-intervention
Respiratory sinus arrhythmia (RSA)
Change from 1 week post-intervention RSA to 1 month post-intervention
Stability of Heart period
Time Frame: Change from 6 months pre-intervention heart period to 1 week pre-intervention
heart period
Change from 6 months pre-intervention heart period to 1 week pre-intervention
Immediate effects of intervention on Heart period
Time Frame: Change from 1 week pre-intervention heart period to 1 week post-intervention
heart period
Change from 1 week pre-intervention heart period to 1 week post-intervention
Short-term effects of intervention on Heart period
Time Frame: Change from 1 week post-intervention heart period to 1 month post-intervention
heart period
Change from 1 week post-intervention heart period to 1 month post-intervention
Stability of Auditory processing
Time Frame: Change from 6 months pre-intervention Filtered Words to 1 week pre-intervention
Filtered Words subtest of SCAN
Change from 6 months pre-intervention Filtered Words to 1 week pre-intervention
Immediate effects of intervention on Auditory processing
Time Frame: Change from 1 week pre-intervention Filtered Words to 1 week post-intervention
Filtered Words subtest of SCAN
Change from 1 week pre-intervention Filtered Words to 1 week post-intervention
Short-term effects of intervention on Auditory processing
Time Frame: Change from 1 week post-intervention Filtered Words to 1 month post-intervention
Filtered Words subtest of SCAN
Change from 1 week post-intervention Filtered Words to 1 month post-intervention
Stability of Auditory processing
Time Frame: Change from 6 months pre-intervention Competing Words to 1 week pre-intervention
Competing Words subtest of SCAN
Change from 6 months pre-intervention Competing Words to 1 week pre-intervention
Immediate effects of intervention on Auditory processing
Time Frame: Change from 1 week pre-intervention Competing Words to 1 week post-intervention
Competing Words subtest of SCAN
Change from 1 week pre-intervention Competing Words to 1 week post-intervention
Short-term effects of intervention on Auditory processing
Time Frame: Change from 1 week post-intervention Competing Words to 1 month post-intervention
Competing Words subtest of SCAN
Change from 1 week post-intervention Competing Words to 1 month post-intervention
Stability of Sensory Sensitivities
Time Frame: Change from 6 months pre-intervention BBC Sensory Scales to 1 week pre-intervention
BBC Sensory Scales (questionnaire)
Change from 6 months pre-intervention BBC Sensory Scales to 1 week pre-intervention
Stability of Latency to Affect recognition
Time Frame: Change from 6 months pre-intervention DARE latency to 1 week pre-intervention
Dynamic Affect Recognition Evaluation (DARE) - latency
Change from 6 months pre-intervention DARE latency to 1 week pre-intervention
Immediate effects of intervention on Latency to Affect recognition
Time Frame: Change from 1 week pre-intervention DARE latency to 1 week post-intervention
Dynamic Affect Recognition Evaluation (DARE) - latency
Change from 1 week pre-intervention DARE latency to 1 week post-intervention
Short-term effects of intervention on Latency to Affect recognition
Time Frame: Change from 1 week post-intervention DARE latency to 1 month post-intervention
Dynamic Affect Recognition Evaluation (DARE) - latency
Change from 1 week post-intervention DARE latency to 1 month post-intervention
Stability of Accuracy of Affect recognition
Time Frame: Change from 6 months pre-intervention DARE accuracy to 1 week pre-intervention
Dynamic Affect Recognition Evaluation (DARE) - accuracy
Change from 6 months pre-intervention DARE accuracy to 1 week pre-intervention
Immediate effects of intervention on Accuracy of Affect recognition
Time Frame: Change from 1 week pre-intervention DARE accuracy to 1 week post-intervention
Dynamic Affect Recognition Evaluation (DARE) - accuracy
Change from 1 week pre-intervention DARE accuracy to 1 week post-intervention
Short-term effects of intervention on Accuracy of Affect recognition
Time Frame: Change from 1 week post-intervention DARE accuracy to 1 month post-intervention
Dynamic Affect Recognition Evaluation (DARE) - accuracy
Change from 1 week post-intervention DARE accuracy to 1 month post-intervention
Stability of Prosody
Time Frame: Change from 6 months pre-intervention prosody to 1 week pre-intervention
Analyses of vocal recordings
Change from 6 months pre-intervention prosody to 1 week pre-intervention
Immediate effects of intervention on Prosody
Time Frame: Change from 1 week pre-intervention prosody to 1 week post-intervention
Analyses of vocal recordings
Change from 1 week pre-intervention prosody to 1 week post-intervention
Short-term effects of intervention on Prosody
Time Frame: Change from 1 week post-intervention prosody to 1 month post-intervention
Analyses of vocal recordings
Change from 1 week post-intervention prosody to 1 month post-intervention
Stability of Disruptive behavior
Time Frame: Change from 6 months pre-intervention DBC to 1 week pre-intervention
Developmental Behavior Checklist (DBC) (questionnaire)
Change from 6 months pre-intervention DBC to 1 week pre-intervention
Immediate effects of intervention on Disruptive behavior
Time Frame: Change from 1 week pre-intervention DBC to 1 week post-intervention
Developmental Behavior Checklist (DBC) (questionnaire)
Change from 1 week pre-intervention DBC to 1 week post-intervention
Short-term effects of intervention on Disruptive behavior
Time Frame: Change from 1 week post-intervention DBC to 1 month post-intervention
Developmental Behavior Checklist (DBC) (questionnaire)
Change from 1 week post-intervention DBC to 1 month post-intervention
Stability of Oxytocin
Time Frame: Change from 6 months pre-intervention oxytocin to 1 week pre-intervention
oxytocin levels derived from salivary sample
Change from 6 months pre-intervention oxytocin to 1 week pre-intervention
Stability of Vasopressin
Time Frame: Change from 6 months pre-intervention vasopressin to 1 week pre-intervention
vasopressin levels derived from salivary sample
Change from 6 months pre-intervention vasopressin to 1 week pre-intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Stephen W Porges, PhD, Indiana University/Kinsey Institute

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2017

Primary Completion (Actual)

March 8, 2023

Study Completion (Actual)

March 8, 2023

Study Registration Dates

First Submitted

March 23, 2017

First Submitted That Met QC Criteria

March 29, 2017

First Posted (Actual)

April 5, 2017

Study Record Updates

Last Update Posted (Actual)

April 3, 2023

Last Update Submitted That Met QC Criteria

March 30, 2023

Last Verified

March 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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