Effect of Music Prehabilitation on Preoperative Anxiety Before Surgery (NCT05982184) | Clinical Trial Compass
CompletedNot Applicable
Effect of Music Prehabilitation on Preoperative Anxiety Before Surgery
Netherlands116 participantsStarted 2023-10-03
Plain-language summary
The goal of this multicenter randomized controlled trial is to investigate the effect of music prehabilitation on preoperative anxiety in patients undergoing elective oncological colorectal resection. Patients will be asked to listen to music three times a day starting one week before day of surgery. Anxiety levels will be compared with the control group that is not explicitly instructed to listen to music by using validated questionnaires
Who can participate
Age range16 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Patients aged ≥ 16 years
* Patients undergoing elective oncological colorectal surgery at participating center
* Minimal hospital stay of 2 days postoperatively.
* Sufficient knowledge of the Dutch language
* Communicable and able to assess the questionnaires
* Patients who have access to personal music playing device and headphones/earphones. - Written informed consent acquired from the patient
Exclusion Criteria:
* Patients with severe hearing impairment (defined as no or barely verbal communication possible).
* Patients with an expected stay of less than two nights in the hospital
* Patients who are professional musicians.
* Active music players or singers who may play or sing every week
* Patients who actively listen to music with a duration of \> 30 minutes daily. Active listening is defined as music listening with headphones/earphones, while this is not combined with any other activity (e.g. exercising, working, driving or religious activities).
* Patients who have a preoperative waiting period of less than five days.
* Participation in another study that may possibly intervene with the outcome measures. (e.g. use of psychiatric medication during inclusion or prehabilitation interventions or similar procedures according to the judgement of the research team)
* Assessment of primary outcome is not possible.
* Patients with mental disorders influencing their ability to adhere to the study protocol and/or assess the questionnaires.
* Inability or u…
What they're measuring
1
Patient reported anxiety measured by the 6-item Spielberger State-trait Anxiety (STAI-6) inventory at admission.
Timeframe: Baseline and day of admittance to hospital