postoperative stress, sleep, pain in patients undergoing elective abdominal surgery
Conditions
Interventions
Group 1: The duration of observation is the period of the postoperative inpatient stay.
The control group does not receive any specific intervention.
Throughout the entire stay, participants’ activity
Sponsors
ukrb
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - patients undergoing elective abdominal surgery at the ukrb - informed consent - ability to independently perform the micro-interventions
Exclusion criteria
Exclusion criteria: - severe pulmonary diseases (e.g., COPD) - severe psychiatric disorders (e.g., anxiety and panic disorders) - postoperative inpatient stay of less than 48 hours - withdrawn informed consent - pregnancy - non-elective surgery - inability to independently perform the micro-interventions
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Postoperative differences in reduction of stress measured by 24h urinary cortisol, smartwatch data and questionnaire 2. Differences in postoperative quality of sleep measured by smartwatch data and questionnaire | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. overall satisfaction in patients 2. intensity of pain and pain medication needed 3. Analysis of the correlation between subjective self-reported and objectively measured physiological parameters | — |
Countries
Germany
Contacts
Public ContactKjell Sonnenberg
ukrb
Outcome results
None listed