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Implementation of music Intervention in the Perioperative standard care (IMRPOVE-study)

Implementation of music Intervention in the perioperative standard care

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON23299
Enrollment
100
Registered
2019-10-08
Start date
2019-11-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal cancer, inflammatory bowel disease (IBD, consisting of Crohn’s disease and ulcerative colitis)

Interventions

Music intervention provided using headphones

Sponsors

Erasmus MC, University Medical Center Rotterdam Department of Surgery P.O. Box 2040, 3000 CA Rotterdam, The Netherlands
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Phase 1 Patients Adult patients who have undergone or will undergo a surgical procedure at the surgical department. In order to be eligible to participate in this study, a subject must meet all of the following criteria: 1. Age = 18 years old 2. Patients who have undergone an elective gastrointestinal (GI) surgical procedure for oncology treatment or inflammatory bowel disease (IBD, consisting of Crohn’s disease and ulcerative colitis (UC)) admitted to the GI nursing department 3. Written informed consent provided by patient or a medical representative of the patient. Health care professionals Institutional health care professionals involved in the perioperative period, including; 1. Surgeons 2. Surgery residents/ fellow’s 3. Anaesthesiologists 4. Nurse anaesthetists 5. Nurses involved in the perioperative process of the patient Phase 3 Music Intervention In order to be eligible to participate in this study, a subject must meet all of the following criteria: 1. Age = 18 years old 2. Patients planned for an elective gastrointestinal (GI) surgical procedure for oncology treatment or inflammatory bowel disease (IBD, consisting of Crohn’s disease and ulcerative colitis (UC)) admitted to the GI nursing department 3. Written informed consent provided by patient or a medical representative of the patient.

Exclusion criteria

Exclusion criteria: Phase 3 Music Intervention A potential subject who meets any of the following criteria will be excluded from participation in this study: 1. Severe hearing impairment causing problems with verbal communication. 2. Patients who are unable or unwilling to receive the music intervention. 3. Patients who do not adequately control the Dutch or English language.

Design outcomes

Primary

MeasureTime frame
The primary outcome is the adherence (%) to the music intervention, by calculating the percentage of patients who consented in receiving the intervention and who truly received the intervention during the implementation phase, and assessing the initial impact of the implementation on pain of the first POD.

Secondary

MeasureTime frame
Secondary outcomes consist of adherence to the implementation strategy, penetration of the intervention in the standard care, assessment of the determinants of practice for implementation and the effect of music on postoperative pain scores during the entire hospitalization, NSAIDs, opioid and sedative medication used perioperatively, postoperative complication, hospital and ICU LOS.

Contacts

Public ContactEllaha Kakar

Erasmus Medical Centre

e.kakar@erasmusmc.nl0628904317

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)