The goal of this observational registry is to systematically collect and analyse real-world clinical and patient-reported data in individuals receiving treatment for acute and chronic pain. The main questions it aims to answer are: How do pain intensity, functional status, and quality of life evolve over time in patients with acute and chronic pain? How are different routine clinical treatment approaches associated with patient-reported outcomes in real-world clinical practice? Participants already receiving standard care for pain management will have routine clinical data recorded as part of their treatment and will be asked to complete standardized questionnaires on pain intensity, functional status, and quality of life at multiple time points during treatment and follow-up. Data are collected using a secure electronic system and are pseudonymised prior to analysis in accordance with Swiss data protection regulations.
Eligibility
Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Signed informed consent by the participant or legal guardian for minors.
* Diagnosis of acute or chronic pain (chronic pain defined as pain lasting ≥ 3 months), including nociceptive, neuropathic, or mixed pain conditions.
* Referral for interdisciplinary outpatient pain assessment or treatment.
* Sufficient proficiency in German, French, Italian, or English to complete digital assessments (parental proxy allowed for paediatric participants if needed).
* All age groups included.
Exclusion Criteria:
* Lack of capacity to provide informed consent or absence of a legal guardian for minors.
* Inability to understand study languages and complete assessments even with assistance.
* Acute life-threatening conditions precluding participation.
* Site-specific safety considerations as determined by treating clinician.
Primary outcome measure(s)
Feasibility of baseline assessment — Baseline (at enrollment) Feasibility is defined as the proportion of eligible participants who complete the full multidomain digital baseline assessment across all predefined domains.
Data quality of baseline assessment — Baseline (at enrollment) Data quality will be evaluated by completeness of core variables of the multidomain digital baseline assessment (percentage of missing data at item and domain level).
Trial sites (1)
Facility
City
Region
Status
Universitätsklinik für Anästhesiologie und Schmerzmedizin, Inselspital, Universitätsspital Bern
Bern
Canton of Bern
More Insel Gruppe AG, University Hospital Bern trials in Switzerland
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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