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What do patients in an interdisciplinary multimodal chronic pain therapy setting perceive as helpful?

What do patients in an interdisciplinary multimodal chronic pain therapy setting perceive as helpful? - /

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00021282
Enrollment
100
Registered
2020-08-31
Start date
2020-05-27
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

R52.1 R52.2

Interventions

Group 1: Observational study: patients with chronic pain are asked about their opinion and pain-related experience on the basis of questionnaires. The following questionnaires will be handed out at th
Day 14: type, severity and duration of pain, ODI, HADS-D, SF-12, FABQ, FESS, therapy elements perceived as helpful with justification, motivation to carry out the remaining treatment units, therapies
day 28 (end of day clinic treatment): type, severity and duration of pain, therapy elements perceived as helpful with justification, therapies carried out for the future including offers from the day
day 90 (follow-up) : Type, severity and duration of pain, continued treatment Forms made during the last 3 months including made / added, (not) realized, ODI, HADS-D, SF-12, FABQ, FESS.

Sponsors

Bereich konservative Orthopädie und Schmerztherapie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: - Pain symptoms without acute neurological deficits and without radicular components - Duration of complaint > 12 weeks for conservative therapy - Capable of working or retired temporarily / permanently due to reduced earning capacity or retired due to age - Ability to give consent

Exclusion criteria

Exclusion criteria: - Signs of inflammatory activity of bacterial or rheumatological origin - Existence of acute neurological deficits, tumor disease - Relevant secondary illnesses with regard to impairment of the ability to consent, exercise or exercise capacity

Design outcomes

Primary

MeasureTime frame
The main target variable is the value of the von Korff scale describing the stages of chronic pain.

Secondary

MeasureTime frame
English: Other variables are: - which therapy modules are rated as helpful by the patient (Likert scales for each therapy unit), - How many therapy modules were rated as helpful by the patients and whether this had an effect on depression (HADS-D), everyday activity (Oswestry Disability Index), quality of life (SF-12), self-efficacy despite pain (FESS) and avoidance behavior (FABQS) Has. - Which resolutions were really implemented after the therapy (comparing answers from questionnaire after 4 weeks (discharge) and after 3 months (follow-up)) - and how this affects the main target variable (stage of chronification).

Countries

Germany

Contacts

Public ContactEva Neubauer

Bereich konservative Orthopädie und Schmerzmedizin

Eva.Neubauer@med.uni-heidelberg.de.06221/56-29289

Outcome results

None listed

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