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CompletedNCT04104217Updated Aug 22, 2023

A Study of the Experience of Music Therapy in Cancer Patients With Delirium

An observational study in Cancer Patients With Delirium, sponsored by Memorial Sloan Kettering Cancer Center. Completed at 1 site in United States. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2023-08-22.

Sponsored by Memorial Sloan Kettering Cancer Center · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
17
Ages
18 Years to 75 Years
Sex
All
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Study summary

The purpose of this study is to improve our understanding of the experience of music therapy by cancer patients with delirium, and the experience of music therapists working with these patients. The researchers are focusing on patients with delirium because of the challenging symptoms of this condition.

At MSK, music therapy is routinely used in patients with cancer. Music therapy sessions are done at the patient's bedside, where the music therapist plays live music on a guitar, keyboard, harp, or percussion instrument, sometimes as accompaniment to singing.

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Conditions studied

  • Cancer Patients With Delirium

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Keywords

  • Music therapy
  • 19-270
03

In context

Delirium

1,057 studies on the registry are indexed under Delirium; 238 are open to participants now.

This study's enrollment of 17 is below the median of 200 across 418 observational studies indexed under Delirium.

Browse Delirium studies →

Lead sponsor

Memorial Sloan Kettering Cancer Center is the lead sponsor of 1,930 studies on the registry; 325 are open to participants now.

Of its 129 completed or terminated interventional studies of FDA-regulated products, 66 (51%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patient subjects who are referred for music therapy will be identified to the researcher by a board-certified music therapist on staff at MSKCC (excluding the Principal Investigator).

Inclusion criteria

  • adult patients (ages 18-75) with delirium
  • referred for and receive music therapy.
  • were identified as having delirium by the Confusion Assessment Method (CAM), Confusion Assessment Method for ICU patients (CAM-ICU) or a documented diagnosis by a clinician from the Department of Psychiatry and Behavioral Sciences in the patient's electronic medical record (EMR).
  • Patients that have had music therapy in the past will be eligible for the study
  • Only patients that recover from delirium (per CAM, CAM-ICU, or progress note by a clinician from the Department of Psychiatry and Behavioral Sciences) after receiving music therapy will be approached for interview by the researcher.

This study will also include their caregivers, music therapists, primary nurse, and bedside companions who have participated in or observed the participants' response to music therapy.

The music therapist participants are:

  • Board-certified senior music therapists with 10 or more years experience in the research site who sign a blanket consent form to participate in study.
  • Assigned to eligible patients by Integrative Medicine Service Client Service Representative (CSR).

The caregivers are:

  • Family or unrelated adult (>18) caregivers who observed bedside music therapy session(s) with patients meeting inclusion criteria

The staff caregivers are:

  • Primary nurse caring for eligible patients who receive their first music therapy session while experiencing delirium.
  • Patient care technicians (PCT) assigned as bedside companions for eligible patients who receive music therapy

Exclusion criteria

Exclusion Criteria:

  • have a known hearing impairment
  • do not speak English.
  • are heavily sedated, comatose, or expected to be discharged or expire within 48 hours
  • have known comorbidities of delirium tremens, steroid psychosis, or dementia

Caregivers will be excluded from the study if they do not speak English. Music therapists, nurses, or bedside companions will be excluded if they are not assigned to eligible patients.

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Study design

Observational model
Other
Time perspective
Prospective
Enrollment
17 participants (actual)
Patient registry
No

Groups and cohorts

  • patients

    Participate in 30-60 minute interviews after each music therapy session.

    Behavioral: Music therapy · Behavioral: Interviews

  • caregivers

    Participate in 30-60 minute interviews after each music therapy session (ideally within 3 days).

    Behavioral: Music therapy · Behavioral: Interviews

  • nurses

    Participate in 10-15 minute interviews after initial music therapy session.

    Behavioral: Music therapy · Behavioral: Interviews

  • music therapists

    Music therapist will notify the researcher if he/she has provided music therapy for a patient who is identified as having delirium. Music therapists will also be interviewed about the clinical process after initial and follow up music sessions.

    Behavioral: Interviews

Interventions

  • BehavioralMusic therapy

    Music therapy sessions may last 20-60 minutes, with length and frequency to be determined mutually (generally 1-3 times per week). Music therapy sessions are done at the patient's bedside, where the music therapist plays live music on a guitar, keyboard, harp, or percussion instrument, sometimes as accompaniment to singing.

  • BehavioralInterviews

    Each interview will be conducted in person in a private setting (with the exception of caregivers, who have the option to conduct interviews over the phone if it is not feasible to take place in the hospital). Each interview will follow a semi-structured interview guide and will ask for consent to audio record the interviews .

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What researchers measure

Primary outcomes

  1. thematic analysis of data with music therapists

    by interviews

    Time frame: 1 year

Secondary outcomes

  1. thematic analysis of data with caregivers, nurses, and patients

    by interviews

    Time frame: 1 year

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Study locations

1 site
  • Memorial Sloan Kettering Cancer Center
    New York, New York 10065, United States
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References and documents

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 22, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04104217
Lead sponsor
Memorial Sloan Kettering Cancer Center
Collaborators
New York University
Responsible party
Sponsor
First posted
Sep 26, 2019
Start date
Sep 23, 2019
Primary completion
Aug 18, 2023
Completion
Aug 18, 2023
Last update
Aug 22, 2023

Study contacts

Holly Mentzer, MA, LCAT, MT-BC
principal investigator · Memorial Sloan Kettering Cancer Center

Oversight

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

Not currently enrolling

This study is completed, as verified in Aug 2023. You cannot join it, but the record below documents what was studied.

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