post surgical pain
Conditions
Interventions
Group 1: intraoperative audio intervention via headphones under anaesthesia during surgery
Group 2: intraoperative headphone application under anaesthesia during surgery
Sponsors
UK Essen
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Open abdominal surgery - Consent to participate in the study
Exclusion criteria
Exclusion criteria: - Patients with hearing impairment or intolerance to headphones - Diagnosis of dementia, cognitive impairment - Lack of consent - Insufficient knowledge of German - MG 30 (chronic pain), pre-existing
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evidence of a difference in postoperative pain levels (NRS 0-10) within the first 24 hours after surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| - Evidence of a difference in postoperative pain levels (NRS) within the first 2 / 48 hours after surgery between patients with and without intraoperative audio intervention - Demonstration of a difference in postoperative pain medication requirements (morphin equivalents) within the first 2 / 24 / 48 hours after surgery between patients with and without intraoperative audio intervention - Evaluation of patients' subjective treatment expectations. and Investigation of the influence of audio interventions on patient satisfaction (GEEE questionnaire) - Perioperative anaesthesiological regime, e.g. general anaesthesia, regional anaesthesia (procedure) +/- analgosedation - Socio-demographic data, e.g. age, gender, educational level, social status, handedness - Psychological comorbidities: Depression, anxiety disorder (case history) | — |
Countries
Germany
Contacts
Public ContactBeatrice Oehler
UK Essen
Outcome results
None listed