Effectiveness of Music Therapy on Level of Consciousness
Primary Purpose
Neurologic Disorder, Traumatic Brain Injury, Disorder of Consciousness
Status
Recruiting
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Music Stimulation
Alternative Stimulation
No Auditory Stimulation
Sponsored by
About this trial
This is an interventional treatment trial for Neurologic Disorder focused on measuring neurological rehabilitation, music therapy, level of consciousness, default mode network
Eligibility Criteria
Inclusion Criteria:
- early neurological rehabilitation (phase B)
- traumatic brain injury
- disorder of consciousness (coma, UWS, MCS)
- at minimum two weeks after disease onset
- admission to intensive care unit
- written consent from the patient's legal representative
- Exclusion of pregnancy
Exclusion Criteria:
- insufficient cardiorespiratory stability
- fractures or severe infratentorial brain injuries leading to impaired auditory evoked potentials
- previous brain damage
- Known mental disorders (dementia, depression)
- hearing loss or deafness in one or two ears
- wounds that do not allow you to wear headphones
- colonization with multi-resistant pathogens
- MRI contraindications
- claustrophobia
- weight>120 kg
Sites / Locations
- BDH-Clinic Hessisch OldendorfRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Active Comparator
Sham Comparator
Arm Label
Music Stimulation
Alternative Auditory Stimulation
No Auditory Stimulation
Arm Description
Patients preferred music is presented via headphones.
An audio book is presented via headphones.
Silence is presented via headphones.
Outcomes
Primary Outcome Measures
Change in level of consciousness
Level of consciousness is measured with the Coma-Recovery-Scale-Revised (Range: 0 to 23) before and after treatment.
Secondary Outcome Measures
Change in connectivity within the default mode network
Patients undergo a MRI scan before and after intervention. Each MRI scan has a duration of 30 minutes. Functional and structural sequences are measured. The resting-state scan (important for the assessment of the default mode network) has a duration of eight minutes and is performed without external stimulation.
Full Information
NCT ID
NCT04442971
First Posted
June 17, 2020
Last Updated
July 26, 2023
Sponsor
BDH-Klinik Hessisch Oldendorf
1. Study Identification
Unique Protocol Identification Number
NCT04442971
Brief Title
Effectiveness of Music Therapy on Level of Consciousness
Official Title
Investigation of the Effectiveness of Music Therapy on the Level of Consciousness of Neurological Early Rehabilitation Patients
Study Type
Interventional
2. Study Status
Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 15, 2020 (Actual)
Primary Completion Date
June 15, 2024 (Anticipated)
Study Completion Date
December 15, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
BDH-Klinik Hessisch Oldendorf
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
It is known that even in patients with severe disorders of consciousness (DOC), the perception of known stimuli triggers emotional reactions that can be interpreted as an expression of a residual function of consciousness. Music therapy has a long tradition in neurological rehabilitation. Frequently, active therapies with own music making and singing are implemented in clinical settings. In DOC patients, it is more likely to use passive music listening. However, findings on effectiveness are limited, as only a few studies have systematically investigated the effects of music therapy in this population. Therefore, the investigators want to investigate the effectiveness of passive listening to preferred music on the level of consciousness.
Detailed Description
Due to continuous improvements in acute medical care, the number of patients surviving severe brain damage has increased over the past decades. While some patients improve significantly during the first days after the injury, other patients remain in altered states of consciousness (i.e. coma, unresponsive wakefulness syndrome or minimally conscious state). In patients with disorders of consciousness (DOC), the auditory modality is preferably examined because the responsiveness within the motor and visual modality is often difficult to assess or impaired. Music is a special type of auditory stimulation that can be of particular benefit in DOC patients. The positive effects of music are attributed to the restoration of specific brain networks that are necessary for processing sensory inputs, as well as the emotional aspects of music, which can increase arousal and activate the reward system. Previous studies have shown that music, including passive listening to music, is associated with psychological and physical changes in both healthy and clinical populations. For example, listening to preferred music can reduce pain and anxiety and the need for sedation in different patient groups.
Music therapy has a long tradition in neurological rehabilitation. In DOC patients, passive listening to music is used (in contrast to active therapies used in fully conscious patients). Efficacy results are inconsistent, however, since only a few studies have systematically investigated the effects of music therapy. In previous investigations, either the sample size is very small or no control conditions have been used. A study that met both quality criteria was published by Sun & Chen in 2015. The authors compared two groups: while the music group (n = 20) listened to their favorite music for 15 to 30 minutes three times a day for a period of four weeks, the control group received no stimulation. Although the GCS values increased significantly in both groups, the music group showed a significantly stronger improvement in the level of consciousness. Based on this study, the present study wants to compare the effectiveness of passive listening to music with two control conditions (alternative auditory stimulation and no auditory stimulation) in early neurological rehabilitation patients.
It is a prospective, double-blind, controlled and randomized intervention study that is carried out monocentrically. Over a period of 24 months, 66 patients undergoing early neurological and neurosurgical rehabilitation after severe brain damage are included. For the individual patient, the study duration is a maximum of 38 days (preliminary phase: 3-7 days; intervention phase: 28 days; follow-up phase: 1-3 days). Patients are randomly assigned to one of three study arms (1. Musical stimulation; 2. Alternative auditory stimulation, 3. No auditory stimulation). In the preliminary phase (days 1 to 7), a native MRI (without contrast agent) and a CRS-R assessment are performed. In addition, there is a neurophysiological examination in which evoked potentials are recorded. In the subsequent main phase, the intervention takes place: Over a period of 28 days, the study participants wear headphones for 30 minutes a day, through which they are presented with preferred music (experimental arm), an audio book (comparative arm) or silence (control arm). In the main phase, a CRS-R test is carried out weekly to record the current state of consciousness. In the follow-up phase (1 to 3 days), the (native) MRI examination, the CRS-R assessment and the neurophysiological examination are repeated. The primary outcome measure is an improvement of the level of consciousness, measured with the Coma-Recovery-Scale-Revised (CRS-R).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neurologic Disorder, Traumatic Brain Injury, Disorder of Consciousness
Keywords
neurological rehabilitation, music therapy, level of consciousness, default mode network
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
66 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Music Stimulation
Arm Type
Experimental
Arm Description
Patients preferred music is presented via headphones.
Arm Title
Alternative Auditory Stimulation
Arm Type
Active Comparator
Arm Description
An audio book is presented via headphones.
Arm Title
No Auditory Stimulation
Arm Type
Sham Comparator
Arm Description
Silence is presented via headphones.
Intervention Type
Behavioral
Intervention Name(s)
Music Stimulation
Intervention Description
Patients wear headphones for 30 minutes/day over a period of four weeks and listen to their preferred music.
Intervention Type
Behavioral
Intervention Name(s)
Alternative Stimulation
Intervention Description
Patients wear headphones for 30 minutes/day over a period of four weeks and listen to an audio book.
Intervention Type
Behavioral
Intervention Name(s)
No Auditory Stimulation
Intervention Description
Patients wear headphones for 30 minutes/day over a period of four weeks and hear silence.
Primary Outcome Measure Information:
Title
Change in level of consciousness
Description
Level of consciousness is measured with the Coma-Recovery-Scale-Revised (Range: 0 to 23) before and after treatment.
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Change in connectivity within the default mode network
Description
Patients undergo a MRI scan before and after intervention. Each MRI scan has a duration of 30 minutes. Functional and structural sequences are measured. The resting-state scan (important for the assessment of the default mode network) has a duration of eight minutes and is performed without external stimulation.
Time Frame
4 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
early neurological rehabilitation (phase B)
traumatic brain injury
disorder of consciousness (coma, UWS, MCS)
at minimum two weeks after disease onset
admission to intensive care unit
written consent from the patient's legal representative
Exclusion of pregnancy
Exclusion Criteria:
insufficient cardiorespiratory stability
fractures or severe infratentorial brain injuries leading to impaired auditory evoked potentials
previous brain damage
Known mental disorders (dementia, depression)
hearing loss or deafness in one or two ears
wounds that do not allow you to wear headphones
colonization with multi-resistant pathogens
MRI contraindications
claustrophobia
weight>120 kg
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Melanie Boltzmann, PhD
Phone
0049 5152 781 256
Email
m.boltzmann@bdh-klinik-hessisch.oldendorf
First Name & Middle Initial & Last Name or Official Title & Degree
Simone B Schmidt, PhD
Phone
0049 5152 781 215
Email
si.schmidt@bdh-klinik-hessisch.oldendorf
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jens D Rollnik, MD
Organizational Affiliation
BDH-Clinic Hessisch Oldendorf
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Melanie Boltzmann, PhD
Organizational Affiliation
BDH-Clinic Hessisch Oldendorf
Official's Role
Principal Investigator
Facility Information:
Facility Name
BDH-Clinic Hessisch Oldendorf
City
Hessisch Oldendorf
ZIP/Postal Code
31840
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Melanie Boltzmann, PhD
Phone
0049 5152 781 256
Email
m.boltzmann@bdh-klinik-hessisch-oldendorf.de
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
All IPD that underlie results in a publication.
IPD Sharing Time Frame
Period of availability begins when results are published, at the earliest in Dec 2022
IPD Sharing Access Criteria
IPD can be obtained from the principal investigator upon reasonable request.
Citations:
PubMed Identifier
26640445
Citation
Kotchoubey B, Pavlov YG, Kleber B. Music in Research and Rehabilitation of Disorders of Consciousness: Psychological and Neurophysiological Foundations. Front Psychol. 2015 Nov 27;6:1763. doi: 10.3389/fpsyg.2015.01763. eCollection 2015.
Results Reference
background
PubMed Identifier
26284020
Citation
Perrin F, Castro M, Tillmann B, Luaute J. Promoting the use of personally relevant stimuli for investigating patients with disorders of consciousness. Front Psychol. 2015 Jul 30;6:1102. doi: 10.3389/fpsyg.2015.01102. eCollection 2015.
Results Reference
background
PubMed Identifier
26277246
Citation
Hole J, Hirsch M, Ball E, Meads C. Music as an aid for postoperative recovery in adults: a systematic review and meta-analysis. Lancet. 2015 Oct 24;386(10004):1659-71. doi: 10.1016/S0140-6736(15)60169-6. Epub 2015 Aug 12. Erratum In: Lancet. 2015 Oct 24;386(10004):1630.
Results Reference
background
PubMed Identifier
23689789
Citation
Chlan LL, Weinert CR, Heiderscheit A, Tracy MF, Skaar DJ, Guttormson JL, Savik K. Effects of patient-directed music intervention on anxiety and sedative exposure in critically ill patients receiving mechanical ventilatory support: a randomized clinical trial. JAMA. 2013 Jun 12;309(22):2335-44. doi: 10.1001/jama.2013.5670.
Results Reference
background
PubMed Identifier
25912580
Citation
Sun J, Chen W. Music therapy for coma patients: preliminary results. Eur Rev Med Pharmacol Sci. 2015 Apr;19(7):1209-18.
Results Reference
background
Learn more about this trial
Effectiveness of Music Therapy on Level of Consciousness
We'll reach out to this number within 24 hrs