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No Music followed by Patient-Oriented Music Intervention (POMI) - Sequence BA for Critical Illness (POMI_PhaseII Trial)

N/A
Waitlist Available
Led By Céline Gélinas, RN, PhD
Research Sponsored by McGill University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from bed turning (up to 90 minutes post baseline) to 30 minutes post bed turning
Awards & highlights

POMI_PhaseII Trial Summary

Introduction Many patients experience pain in the intensive care unit (ICU) despite receiving pain medication. Research has shown that music can help manage pain. Music interventions that have been studied so far have not been based on patient preferences, recommended tempo and duration, nor used music streaming. It is important that a music intervention take into consideration the expertise of ICU patients, family members and nurses/orderlies. Study objectives This study aims to evaluate the feasibility and acceptability of a new patient-oriented music intervention (POMI) to reduce pain in ICU patients. In addition, the aim is to evaluate the feasibility of conducting a crossover randomized controlled trial (RCT) to test the interventions in the adult ICU. A secondary objective will be to examine the preliminary efficacy of the POMI. Methodology/Study Design A single-blind 2x2 crossover pilot RCT will be used to evaluate the feasibility, acceptability, and preliminary efficacy of the POMI. Patients will undergo a sequence of two intervention periods: the POMI and the Active Control intervention (ACI; headphones/pillow without music). Patients will be randomly assigned to Sequence 1 or Sequence 2, where patients in Sequence 1 receive the POMI during the first intervention period, followed by the ACI in the second intervention period; and patients in Sequence 2 receive the ACI first, followed be the POMI (with a 4-hour washout period). Before the turning procedure, music will be stopped, and the headphones will be removed. For patients able to self-report, the music (or control period without music) will be delivered either via headphones or a music pillow, depending on their individual preference. For patients unable to self-report, music (or control period without music) will be delivered via the music pillow. Twenty-four patients (12 patients able to self-report their pain and 12 patients unable to self-report) will be recruited. The 12 patients able to self-report will be asked about their music preferences and to complete an acceptability questionnaire (AQ). For the 12 patients unable to self-report, 12 family members will be recruited to answer questions on the patient's music preferences and to complete an AQ. In addition, 12 nurses/orderlies (involved in the turning procedure for a patient participant) will be recruited and asked to complete an AQ.

Eligible Conditions
  • Critical Illness
  • Acute Pain
  • Emotional Distress

POMI_PhaseII Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from bed turning (up to 90 minutes post baseline) to 30 minutes post bed turning
This trial's timeline: 3 weeks for screening, Varies for treatment, and from bed turning (up to 90 minutes post baseline) to 30 minutes post bed turning for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Acceptability questionnaire, adapted from the validated Treatment Acceptability and Preferences questionnaire, 0-20 rating scores
Feasibility of intervention delivery
Secondary outcome measures
Change from Baseline Critical-Care Pain Observation Tool (CPOT) at 30 minutes
Change from Baseline Critical-Care Pain Observation Tool (CPOT) at Bed Turning
Change from Baseline Pain distress on the 11-point Numeric Rating Scale (NRS) at 30 minutes
+6 more

POMI_PhaseII Trial Design

2Treatment groups
Experimental Treatment
Group I: Patient-Oriented Music Intervention (POMI) followed by No Music - Sequence ABExperimental Treatment1 Intervention
Patient participants will first receive 20-30 minutes of the patient-oriented music intervention (POMI) first, followed by no music, with a minimal washout period of four hours
Group II: No Music followed by Patient-Oriented Music Intervention (POMI) - Sequence BAExperimental Treatment1 Intervention
Patient participants will first receive no music first, followed by 20-30 minutes of the patient-oriented music intervention (POMI), with a minimal washout period of four hours

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Who is running the clinical trial?

McGill UniversityLead Sponsor
394 Previous Clinical Trials
998,333 Total Patients Enrolled
2 Trials studying Critical Illness
487 Patients Enrolled for Critical Illness
Céline Gélinas, RN, PhDPrincipal InvestigatorMcGill University
1 Previous Clinical Trials
353 Total Patients Enrolled

Frequently Asked Questions

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~16 spots leftby Apr 2025