Music Therapy as a Treatment for Delirium in Acutely Hospitalized Older Patients

Not Applicable

Completed

• Conditions: Delirium of Mixed Origin; Delirium Confusional State; Delirium in Old Age; Delirium Superimposed on Dementia
• Interventions: Behavioral: Preferred Recorded Music (PRM); Behavioral: Preferred Live Music (PLM)

• Registration Number: NCT05398211
• Lead Sponsor: Oslo University Hospital

Brief Summary

The purpose of this study is to assess feasibility and potential effectiveness of two different music interventions for managing delirium symptoms in acute geriatric patients.

Detailed Description

Delirium is a neuropsychiatric syndrome characterized by an acute alteration in attention, awareness, arousal and cognition, precipitated by an acute illness, intoxication, trauma or surgery. It is highly prevalent in older, frail and acutely hospitalized patients, and associated with poor outcomes, with few effective treatment alternatives. Non-pharmacological interventions and music show promising effects.

This study protocol aims to determine whether music interventions (MIs) delivered by a credentialed music therapist, are feasible and effective for regulating delirium symptoms in acute geriatric patients and whether the standardized delirium tools are sensitive to detect observable responses. Primary, feasibility outcomes are evaluating recruitment rate, treatment fidelity and adherence, as well as feasibility and accuracy in data collection procedures. Main effect-outcome is delirium severity, but delirium duration, cognitive status, length of hospital stay, and medication use will also be recorded. The randomised repeated measures controlled trial design will record the participant responses before and after exposure to MIs (+/- 2 hours). Participants with delirium from an acute geriatric ward will be randomized to either live or recorded MI. Each intervention will be delivered to n=30 participants (n=60 in total), for 30 minutes, over three consecutive days. Ethical approval has been obtained from Regional Ethics Committee South East Norway.

Study Timeline

• Study First Submitted: 2022-05-13
• Study First Submitted QC: 2022-05-25
• Study First Posted: 2022-05-31
• Study Start: 2022-06-15
• Primary Completion: 2023-05-31
• Study Completion: 2023-05-31
• Status Verified: 2024-04
• Last Update Submitted: 2024-04-29
• Last Update Posted: 2024-04-30

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 26

Inclusion Criteria

• Aged ≥ 65 and with delirium or possible delirium at admission or detected within the last 72 hours, and still present.
• Appropriate informed consent is obtained.
• Participants will not be excluded if they are under long term care and have comorbidities such as dementia or mild cognitive impairment.
• Patients will not be excluded if they have Covid-19.

Exclusion Criteria

• Patients who were previously enrolled, and were readmitted during the study period will not be re-included.
• The patients with severe hearing impairments, severe psychiatric conditions, and/or severe alcohol/substance addiction where that is the main reason for admission will be excluded.
• The patients whose assessed musical preferences involve orchestral or other kinds of music which cannot be performed live by voice and a guitar.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Preferred Recorded Music (PRM)	Preferred Recorded Music (PRM)	The Preferred Live Music (PLM) aims to elicit participants' responses from live music and the ensuing musical and non-musical interactions with the music therapist (MT). In the PLM intervention, preferred songs performed live on guitar or electronic keyboard will be played by a credentialed MT. When appropriate participants may also play percussion instruments offered to them. Elements of improvisation will be incorporated to allow for active engagement by the participants, and to provide opportunities for musical and non-musical attunement to emerge.
Preferred Live Music (PLM)	Preferred Live Music (PLM)	The Preferred Recorded Music (PRM) intervention aims to detect responses directly attributable to the music. Participants listen to pre-recorded preferred originally-published versions of music accessed by Spotify music-streaming service and played through loud-speakers. The MT will only start the music, and otherwise not be present during the interventions to ensure the minimal direct interaction with the participants.

Primary Outcome Measures

Name	Time	Method
Recruitment rate	Up to 52 weeks	How many participants were recruited and randomized per month on average from those eligible, calculated by dividing the total number of the participants recruited by the total number of months that the trial recruited for.
Treatment fidelity rating and internal and external validity of the study	Up to 52 weeks	The level of treatment fidelity will be determined using NIH Behavioral Change Consortium questionnaire which assesses 5 mutually exclusive categories: study design, training, delivery, receipt, and enactment. The tool lists 25 fidelity attributes that should be rated dichotomously as:" Present", "Absent but should be present", or "Not applicable".
Retention and attrition rates	Up to 52 weeks	Retention is defined as trial completion on study intervention, and will be calculated by dividing the number of participants completing the study by the total number of participants recruited. Attrition rates will be estimated by the percentage of participants that withdrew from the study, and calculated by dividing the number of the participants who withdrew by the total number recruited.
Adherence and deviations rates	Up to 52 weeks	Adherence to the study protocol is defined as compliance with the described study protocol, and protocol deviations as any change or divergence from the study protocol for each participant. Adherence rate will be estimated by calculating the percentage of the music sessions (interventions) actually completed from those described in the protocol (by dividing the number of completed sessions by the number of planned sessions), and deviation rates will be measured by counting the deviations per participant during their participation in the study.

Secondary Outcome Measures

Name	Time	Method
Length of hospital stay	Up to 3 weeks.	The total number of days from admittance to the Acute Geriatric Department to discharge from hospital.
Delirium severity	Up to 7 days	Delirium severity as assessed by Observational Scale of Level of Arousal (OSLA), Richmond Agitation Sedation Scale (RASS).
Cognitive status	Up to 7 days.	Pre-post interventions changes in attention, orientation and short-term memory, assessed by backwards tests and digit span tests, recall tasks and orientation questions from Memorial Delirium Assessment Scale-MDAS)
Use of "rescue medication" during hospital stay	Up to 3 weeks.	The total number of psycho-pharmacological medications per patients will be registered.
Duration of delirium during hospital stay	Up to 3 weeks.	As diagnosed according to Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5) criteria

Trial Locations

Locations (1)

Oslo University Hospital; 🇳🇴 Oslo, Norway