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patient oriented.graduated.interdisciplinary.network - PAIN2020

patient oriented.graduated.interdisciplinary.network - PAIN2020 - PAIN2020

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
DRKS
Registry ID
DRKS00015443
Enrollment
4500
Registered
2019-01-08
Start date
2019-02-02
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

pain and risk for chronicity

Interventions

Group 1: primary data: interdisciplinary multimodal assessment is the core intervention of the new health care provision. Physicians, physiotherapists and psychologist work integretatly on a comprensi

Sponsors

Deutsche Schmerzgesellschaft e.V. (Konsortialführung)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1) min age 18 years 2) pain since at least for 6 weeks OR recurrent pain despite specialized treatment 3) limitation of daily life and percieved health related quality of life because of pain 4) risk for chronicity of pain 5) actual sick leave of at least 4 weeks OR cumulative sick leave of at least 6 weeks during the past 12 months 6) pain relevant diagnosies regarding localization and other conditions 7) pending decision about surgery procedures 8) extensive medical utilization of health care system

Exclusion criteria

Exclusion criteria: 1) cancer of any kind 2) relevant psychological or psychiatric disorder 3) already existing history of chronic pain in the past/actual

Design outcomes

Primary

MeasureTime frame
pain intensity (subscale characteristic pain intensity, grading chronic pain stages, von Korff), pain related limiation of function (subscale disability, grading chronic pain stages, von Korff), treatment effectiveness (global change item of the German Pain Questionnaire, Satisfaction with therapy questionnaire, ZUF8) from patient perspective are primary endpoints. They will be assessed at admission (except treatment effectiveness), 3 and 6 months follow up via self report questionnaire.

Secondary

MeasureTime frame
psychological distress, sick leave (days), health related quality of life, early retirement, direct costs (health policy) will be secondary endpoints. They will be assessed at admission and 3 resp. 6 months follow up via questionnaire, except early retirement and direct costs will be estimated via secondary analyses by the involved cost payer (BARMER).

Countries

Germany

Contacts

Public ContactKatharina Augustin

Deutsche Schmerzgesellschaft e.V.

pain2020@dgss.org+49 (0)30 39409689-5

Outcome results

None listed

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