Effects of Early Musical Intervention on Prevalence and Severity of Paroxysmal Sympathetic Hyperactivity After Severe Traumatic Brain Injury (MUSIC-TCNV)
Primary Purpose
Paroxysmal Sympathetic Hyperactivity
Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Musical intervention
Control
Sponsored by
About this trial
This is an interventional prevention trial for Paroxysmal Sympathetic Hyperactivity focused on measuring Music therapy, Paroxysmal sympathetic hyperactivity, Traumatic brain injury
Eligibility Criteria
Inclusion Criteria:
- Severe traumatic brain injury (either initial Glasgow Coma Scale < 8 or intracranial pressure > 20mmHg for more than 20 min)
- National health service coverage
- Informed consent signed by next of kin
Exclusion Criteria:
- Non-traumatic brain injury
- Conditions interfering with measures: bilateral fixed pupils, temporal bone fracture including acoustic channel, eye trauma, previous eye surgery, otorrhagia, hypoacusis,
- Preexisting autonomic nervous system imbalance: severe diabetes, arrhythmias, pace maker, implantable defibrillator, cardiac transplantation
- Respiratory rate < 9/min
- Patient subject to guardianship or wardship
- Pregnant or breastfeeding woman
- Current participation in another biomedical research protocol
Sites / Locations
- Service d'Anesthésie Réanimation- Hôpital de Hautepierre
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Sham Comparator
Arm Label
Musical intervention
Control
Arm Description
Music is provided through headphones: Two 30-min musical sessions per day (one in the morning and one in the evening) beginning at the onset of desedation (Day 0) until day 21. Both have inverted "U" shape.
Patients wear headphones twice a day during 30 minutes, starting at the onset of desedation (Day 0) until day 21, but no music is provided (blank playlist): Sham
Outcomes
Primary Outcome Measures
Paroxysmal Sympathetic Hyperactivity Assessment Measure [PSH-AM] (ranging from 0 to 29)
The PSH-AM combines the sum of Clinical Features Scale [CFS] (from 0 to 18) and the Diagnostic Likelihood tool [DLT] (from 0 to 11)
Secondary Outcome Measures
Area under the Clinical Features Scale curve
Mean Analgesia Nociception Index
Neurological Pupil Index
Pain (Critical-Care Pain Observation Tool)
Neurological outcome (Wessex Head Injury Matrix)
PSH-AM
Disability Rating Scale
Full Information
NCT ID
NCT02783105
First Posted
May 23, 2016
Last Updated
November 8, 2021
Sponsor
University Hospital, Strasbourg, France
Collaborators
Fondation Apicil, MDMS, Association française des traumatisés crâniens d'Alsace, Association strasbourgeoise des médecins et infirmiers en anesthésie réanimation
1. Study Identification
Unique Protocol Identification Number
NCT02783105
Brief Title
Effects of Early Musical Intervention on Prevalence and Severity of Paroxysmal Sympathetic Hyperactivity After Severe Traumatic Brain Injury
Acronym
MUSIC-TCNV
Official Title
Effects of Early Musical Intervention on Prevalence and Severity of Paroxysmal Sympathetic Hyperactivity After Severe Traumatic Brain Injury: the Prospective Randomized MUSIC-TCNV Trial.
Study Type
Interventional
2. Study Status
Record Verification Date
November 2016
Overall Recruitment Status
Terminated
Why Stopped
inclusion difficulties
Study Start Date
November 20, 2016 (Actual)
Primary Completion Date
January 4, 2019 (Actual)
Study Completion Date
December 18, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Strasbourg, France
Collaborators
Fondation Apicil, MDMS, Association française des traumatisés crâniens d'Alsace, Association strasbourgeoise des médecins et infirmiers en anesthésie réanimation
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Paroxysmal sympathetic hyperactivity (PSH) is a frequent symptom after traumatic brain injury and concerns up to 30% of severely brain-injured patients.
PSH is due to unbalanced autonomic nervous system activity, resulting in sympathetic surges causing hypertension, tachycardia, sweating and hypertonia. The affected patients suffer more pain, more cardiovascular distress, more infections and prolonged rehabilitation and mechanical ventilation; additionally it could lead to a worse outcome.
Classical music was shown to reduce autonomic nervous system imbalance in healthy people and in many medical diseases. It could be a means to dampen sympathetic surges for brain-injured patients presenting with PSH, as well.
Our study aims at demonstrating that early musical intervention, started with the weaning of sedation, can reduce both the prevalence and the severity of paroxysmal sympathetic hyperactivity in traumatic brain-injured patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Paroxysmal Sympathetic Hyperactivity
Keywords
Music therapy, Paroxysmal sympathetic hyperactivity, Traumatic brain injury
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
11 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Musical intervention
Arm Type
Experimental
Arm Description
Music is provided through headphones: Two 30-min musical sessions per day (one in the morning and one in the evening) beginning at the onset of desedation (Day 0) until day 21.
Both have inverted "U" shape.
Arm Title
Control
Arm Type
Sham Comparator
Arm Description
Patients wear headphones twice a day during 30 minutes, starting at the onset of desedation (Day 0) until day 21, but no music is provided (blank playlist): Sham
Intervention Type
Other
Intervention Name(s)
Musical intervention
Intervention Type
Other
Intervention Name(s)
Control
Intervention Description
Patients wear headphones twice a day during 30 minutes, starting at the onset of desedation (Day 0) until day 21, but no music is provided (blank playlist): Sham
Primary Outcome Measure Information:
Title
Paroxysmal Sympathetic Hyperactivity Assessment Measure [PSH-AM] (ranging from 0 to 29)
Description
The PSH-AM combines the sum of Clinical Features Scale [CFS] (from 0 to 18) and the Diagnostic Likelihood tool [DLT] (from 0 to 11)
Time Frame
from desedation (Day 0) to Day 21.
Secondary Outcome Measure Information:
Title
Area under the Clinical Features Scale curve
Time Frame
from Day 0 to Day 21.
Title
Mean Analgesia Nociception Index
Time Frame
from Day 0 to Day 21.
Title
Neurological Pupil Index
Time Frame
from Day 0 to Day 21.
Title
Pain (Critical-Care Pain Observation Tool)
Time Frame
from Day 0 to Day 21.
Title
Neurological outcome (Wessex Head Injury Matrix)
Time Frame
from Day 0 to Day 21.
Title
PSH-AM
Time Frame
Six and twelve months
Title
Disability Rating Scale
Time Frame
Six and twelve months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Severe traumatic brain injury (either initial Glasgow Coma Scale < 8 or intracranial pressure > 20mmHg for more than 20 min)
National health service coverage
Informed consent signed by next of kin
Exclusion Criteria:
Non-traumatic brain injury
Conditions interfering with measures: bilateral fixed pupils, temporal bone fracture including acoustic channel, eye trauma, previous eye surgery, otorrhagia, hypoacusis,
Preexisting autonomic nervous system imbalance: severe diabetes, arrhythmias, pace maker, implantable defibrillator, cardiac transplantation
Respiratory rate < 9/min
Patient subject to guardianship or wardship
Pregnant or breastfeeding woman
Current participation in another biomedical research protocol
Facility Information:
Facility Name
Service d'Anesthésie Réanimation- Hôpital de Hautepierre
City
Strasbourg
ZIP/Postal Code
67098
Country
France
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Effects of Early Musical Intervention on Prevalence and Severity of Paroxysmal Sympathetic Hyperactivity After Severe Traumatic Brain Injury
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