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Validation and application of a core set of patient-relevant outcome domains to assess the effectiveness of multimodal pain therapy (VAPAIN) Sub-study: Validation of candidate instruments to assess patient relevant core domains in the setting of Multimodal Pain Therapy

Validation and application of a core set of patient-relevant outcome domains to assess the effectiveness of multimodal pain therapy (VAPAIN) Sub-study: Validation of candidate instruments to assess patient relevant core domains in the setting of Multimodal Pain Therapy - VAPAIN

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00009600
Enrollment
360
Registered
2017-01-17
Start date
2015-03-01
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

Approval of psychometric properties of common scales to assess pain intensity in patients with chronic pain attending a multimodal pain therapy

Interventions

Group 1: quantitative validation Patients receive a set of questionnaires three times during routine documentation ot the specific institutions (Admission, discharge, follow up) consisting of: 1. Pai

Sponsors

Universitätsklinikum Carl Gustav Carus Dresden
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Study population for quantitative part All patients fulfilling the following inclusion criteria: age = 18 years, chronic permanent or recurrent pain for at least 6 months, not sufficiently satisfied in symptom reduction by previous unimodal pain therapy appraoches (commonly minimum 3 attemps) indicating necessity of a multimodal pain Treatment Approach, medium or high impairment of physical and psychological functioning, sufficient capability to tolerate physical activation, and sufficient skills in German language assessed by an interdisciplinary team in one of four cooperating German comprehensive pain center. Study population for qualitative part All patients fulfilling the following inclusion criteria: age = 18 years, chronic permanent or recurrent pain for at least 3 months, medium or high impairment of physical and psychological functioning, sufficient capability to tolerate physical activation, and sufficient skills in German language assessed by an interdisciplinary team in one of four cooperating German comprehensive pain center. Further to be included into the qualitative validation study (focus groups) patients have to have completed a multimodal pain program and have to be discharged at least for 3 months and not more than 9 months (including booster week if available).

Exclusion criteria

Exclusion criteria: patients not participating in multimodal pain therapy

Design outcomes

Primary

MeasureTime frame
psychometric properties (validity, reliability, sensitivity to Change) of common scales to assess pain intensity in patients with chronic pain attending a multimodal pain therapy supplemented by emotional wellbeing and a specific form of the Short Form 12. NRS pain intensity NRS pain frequency NRS interference because of pain Chronic pain grade: “Characteristic Pain Intensity” McGill Questionnaire “Present Pain Intensity” Multidimensional Pain Inventory: “Pain Severity” SF 36 Subskala “Bodily Pain” Obstacles for return to work “pain intensity” Depression-Anxiety-Stress-Scale SF 12

Secondary

MeasureTime frame
not planned

Countries

Germany

Contacts

Public ContactUlrike Kaiser

UniversitätsSchmerzCentrumUniversitätsklinikum Carl Gustav Carus

ulrike.kaiser.usc-tkl@uniklinikum-dresden.de0351 458 4547

Outcome results

None listed

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