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Pilot study on the validity and satisfaction of app-based questionnaire surveys of pain localization, experience and postoperative recovery in patients after surgery

Pilot study on the validity and satisfaction of app-based questionnaire surveys of pain localization, experience and postoperative recovery in patients after surgery - AiDolor

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00035551
Enrollment
100
Registered
2024-11-22
Start date
2024-06-27
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

Only the operating department, the place of surgery and the size of the operation are recorded. The underlying diseases according to ICD-10 are not recorded.

Interventions

Group 1: Inpatients who have undergone surgery in the Department of Surgery at Ulm University Hospital in one of the following departments: Department of General and Visceral Surgery, Department of Tr
Radbruch L et al. 1999) and on postoperative recovery (Quality of Recovery Questionnaire (Qor-15)
Myles et al., 1999, Kahl et al. 2021). Both questionnaires were completed by the participants both as paper questionnaires and digitally on a smartphone. The order of completion is randomized. Satisfa

Sponsors

Sektion Schmerztherapie, Klinik für Anästhesiologie und Intensivmedizin, Universitätsklinikum Ulm
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Surgery at Ulm University Hospital at the CKL Surgical Clinic (Clinic for General and Visceral Surgery, Clinic for Trauma, Hand, Plastic and Reconstructive Surgery, Clinic for Neurosurgery, Clinic for Urology)

Exclusion criteria

Exclusion criteria: Patients who are unable to give consent Lack of written consent Insufficient digital competence Understanding or communication difficulties, relevant language barrier, so that it is not possible to complete a questionnaire Relevant cognitive impairment, so that it is not possible to complete a questionnaire Children and adolescents < 18 years of age Patients in the final stages of a tumor disease Emergency operations Patients requiring intensive care Planned postoperative mechanical ventilation Cranial interventions Relevant movement disorders of the upper extremities, e.g. coordination disorder or tremor, paralysis, etc. Operations on the leading upper extremity Obstetrics patients Cardiac surgery

Design outcomes

Primary

MeasureTime frame
Consistency of pain localization, experience and recovery in the postoperative phase Paper form and in digital smartphone format.

Secondary

MeasureTime frame
Satisfaction with and efficiency of the digital smartphone format

Countries

Germany

Contacts

Public ContactHannes Hofbauer

Sektion Schmerztherapie, Klinik für Anästhesiologie und Intensivmedizin, Universitätsklinikum Ulm

hannes.hofbauer@uni-ulm.de0049 731 50060033

Outcome results

None listed

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