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Multimodal pain recognition for intermediate care patients in the postoperative waking phase

Multimodal pain recognition for intermediate care patients in the postoperative waking phase

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00023555
Enrollment
50
Registered
2020-11-19
Start date
2020-09-29
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Patients for whom a surgical intervention is planned within the next 3 days.

Interventions

Group 1: A multimodal data collection on patients is carried out with recording of pain over time, including the intensification of drug-based pain therapy. - Data acquisition at the IOI of the Ulm
- Statistical methods and machine learning methods
- publication. Course of studies: 1. examination of the inclusion and exclusion criteria 2. informing patients about the currently valid version of the Declaration of Helsinki in oral and written for

Sponsors

Sektion Medizinische PsychologieKlinik für Psychosomatische MedizinUniversitätsklinikum Ulm
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Men and women aged > 18 years; - All-round oriented patients capable of providing information preoperatively; - Surgical intervention is planned within the next 3 days. Due to the size and/or comorbidities, monitoring in the intensive or intermediate care unit is necessary; - Written consent of the patient to the study; - Start of data collection is the measurement of the preoperative signal level in terms of a baseline measurement; - The next measurement phase takes place postoperatively with the patient awake again, postoperatively for a maximum of 24 hours.

Exclusion criteria

Exclusion criteria: - pregnancy; - Neurological diseases associated with a restriction of peripheral conduction of stimuli such as - Cross-sectional symptoms - Muscular dystrophy - Polyneuropathy (also in advanced diabetes mellitus, C2 abusus) - Critical Illness Polyneuropathy (CIP) - clinical suspicion, - multiple sclerosis, Guillain-Barré syndrome, denervative neurological diseases - Cardiac pacemakers or electric defibrillators - no damage to such devices by the applied currents has so far been proven. We want to avoid potential damage to the devices and thus endangering the patient in any case! - Subsequently withdrawn consent to participate in the study.

Design outcomes

Primary

MeasureTime frame
The multimodal biosignal manifestation differs significantly from the intensity of pain (subjective or external observation).

Secondary

MeasureTime frame
Pain intensities can be trained and recognised using machine learning methods (algorithms of artificial intelligence).

Countries

Germany

Contacts

Public ContactSteffen Dr. Walter

Sektion Medizinische Psychologie Klinik für Psychosomatik und PsychotherapieUniversitätsklinikum Ulm

steffen.walter@uni-ulm.deDE +49 0731 500 61910

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026