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RecruitingNCT04442971Updated Sep 19, 2025

Effectiveness of Music Therapy on Level of Consciousness

An interventional study of Music Stimulation and Alternative Stimulation in Neurologic Disorder, Traumatic Brain Injury and Disorder of Consciousness, sponsored by BDH-Klinik Hessisch Oldendorf. Recruiting at 1 site in Germany. Open to participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2025-09-19.

Sponsored by BDH-Klinik Hessisch Oldendorf · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
66
Allocation
Randomized
Ages
18 Years to 85 Years
Sex
All
01

Study 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.

Read the 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).

02

Conditions studied

  • Neurologic Disorder
  • Traumatic Brain Injury
  • Disorder of Consciousness

Keywords

  • neurological rehabilitation
  • music therapy
  • level of consciousness
  • default mode network
03

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
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
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
66 participants (estimated)

Study arms

  • Experimental
    Music Stimulation

    Patients preferred music is presented via headphones.

    Behavioral: Music Stimulation

  • Active comparator
    Alternative Auditory Stimulation

    An audio book is presented via headphones.

    Behavioral: Alternative Stimulation

  • Sham comparator
    No Auditory Stimulation

    Silence is presented via headphones.

    Behavioral: No Auditory Stimulation

Interventions

  • BehavioralMusic Stimulation

    Patients wear headphones for 30 minutes/day over a period of four weeks and listen to their preferred music.

  • BehavioralAlternative Stimulation

    Patients wear headphones for 30 minutes/day over a period of four weeks and listen to an audio book.

  • BehavioralNo Auditory Stimulation

    Patients wear headphones for 30 minutes/day over a period of four weeks and hear silence.

05

What researchers measure

Primary outcomes

  1. Change in level of consciousness

    Level of consciousness is measured with the Coma-Recovery-Scale-Revised (Range: 0 to 23) before and after treatment.

    Time frame: 4 weeks

Secondary outcomes

  1. 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.

    Time frame: 4 weeks

06

Study locations

1 of 1 sites recruiting
07

References and documents

Publications

  • 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. PubMed 26640445 ↗
  • 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. PubMed 26284020 ↗
  • 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. PubMed 26277246 ↗
  • 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. PubMed 23689789 ↗
  • Sun J, Chen W. Music therapy for coma patients: preliminary results. Eur Rev Med Pharmacol Sci. 2015 Apr;19(7):1209-18. PubMed 25912580 ↗

Individual participant data

Plan to share: Yes — All IPD that underlie results in a publication.

Supporting information: Study protocol, Sap, Icf

08

Registry details

Key details

Study ID
NCT04442971
Lead sponsor
BDH-Klinik Hessisch Oldendorf
Responsible party
Sponsor
First posted
Jun 23, 2020
Start date
Jun 15, 2020
Primary completion
Jun 15, 2026 (estimated)
Completion
Dec 15, 2026 (estimated)
Last update
Sep 19, 2025

Study contacts

Melanie Boltzmann, PhD
Contact
m.boltzmann@bdh-klinik-hessisch.oldendorf
0049 5152 781 256
Simone B Schmidt, PhD
Contact
si.schmidt@bdh-klinik-hessisch.oldendorf
0049 5152 781 215
Jens D Rollnik, MD
study director · BDH-Clinic Hessisch Oldendorf
Melanie Boltzmann, PhD
principal investigator · BDH-Clinic Hessisch Oldendorf

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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