Implementation of music Intervention in the Perioperative standard care (IMRPOVE-study)
- Conditions
- Colorectal cancer, inflammatory bowel disease (IBD, consisting of Crohn’s disease and ulcerative colitis)
- Registration Number
- NL-OMON23299
- Lead Sponsor
- Erasmus MC, University Medical Center Rotterdam Department of Surgery P.O. Box 2040, 3000 CA Rotterdam, The Netherlands
- Brief Summary
ot applicable
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 100
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.
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.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method