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Multimodal complex treatment in a subgroup of patients with vertebral pain syndroms

Multimodal complex treatment in a subgroup of patients with vertebral pain syndroms - ANOA Study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
DRKS
Registry ID
DRKS00011492
Enrollment
181
Registered
2017-01-11
Start date
2013-08-08
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

M40-M54

Interventions

Group 1: patients with chronic back pain with differnent grades of chronicity (MPSS) multimodal treatment OPS code 8-977 Multimodal nonsurgical complex treatment of the musculoskeletal system - inte

Sponsors

ANOA – Krankenhaus GmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: musculoskeletal vertebral pain syndrome with or without spread pain presence of disorders on at least two levels: complex functional findings, e.g. - linkages and / or - coordination disorders and / or - disorders of the posture / motion stabilization - vegetative disorders morphological disorders, e.g. - degenerative changes in the spine - intervertebral disc disorders - spinal stenosis psychosocial factors, e.g. - dysfunctional illness cognitions and behaviors - psychosocial influences on pain development

Exclusion criteria

Exclusion criteria: pain syndrome on the basis of advanced arthrosis with absolute surgical indication neurological system diseases rheumatic / inflammatory diseases tumor diseases pain on internist basis mental disorders as secondary diagnoses and psychosocial influences, if there is a highly significant influence on the development of the disease neurological deficits symptoms (radicular syndrome) with absolute surgical indication polyneuropathies pregnancy, lactation severe cardiopulmonary insufficiency (NYHA III and IV) mental illness as the main diagnosis, including F45.40 and F45.41 running pension process

Design outcomes

Primary

MeasureTime frame
pain intensity (aktual pain intensity, worst pain, average pain, mean of the pain intensity) (v. Korff-- Graded chronic pain status) The data were collected at the following measuring time points (MTP): T1 (before the intervention / baseline), T2 (end of intervention), T3 (6 months after the end of the intervention) and T4 (12 months after the end of the intervention).

Secondary

MeasureTime frame
Quality of life: SF 12 functionality: Oswestry Disability Index Pain Disability Index psychometry: HADS-D FF-Stabs Die Datenerhebung erfolgte an den folgenden Messzeitpunkte (MZP): T1: vor der Intervention, T2: am Ende der Intervention, T3: 6 Monate nach Interventionsende, T4: 12 Monate nach Interventionsende

Countries

Germany

Contacts

Public ContactAnke Steinmetz

Muskuloskeletales Zentrum undKonservative OrthopädieLoreley-Kliniken St. Goar-Oberwesel

A.Steinmetz@loreley-kliniken.de06741/ 800-205

Outcome results

None listed

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