Skip to content

Subproject 2: Musculoskeletal simulations towards a subject-specific spino-pelvic load transfer prediction

Subproject 2: Musculoskeletal simulations towards a subject-specific spino-pelvic load transfer prediction - dyn3M – SP2

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00028773
Enrollment
320
Registered
2022-04-12
Start date
2022-03-01
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

M54.5

Interventions

Group 1: Non-clinical population with chronic non-specific back pain, with chronic specific back pain and without back pain. Assessment of body measures, muscle activity (surface EMG) as well as body

Sponsors

BIH - Julius Wolff Institut für Biomechanik und Muskuloskeletale Regeneration
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Written consent to participate in the study Asym. (no LBP) and symptomatic (chronic LBP) Caucasian women and men aged 18-64 years. Pain duration >12 weeks Pain location: lumbar-pelvic region

Exclusion criteria

Exclusion criteria: Professional, competitive and elite athletes Acute infections Abuse of addictive substances Pregnancy BMI >28 kg/m2 Central or peripheral neurological impairments (e.g., spinal cord injuries, radicular symptoms, sensory deficits) Irritated, inflamed and infected tissue in the measurement areas of the back Fractures of the spine Osteoporosis Tumor diseases and bone metastases Previous operations on the spine Heavy drug therapy (opioids, muscle relaxants, antiepileptic drugs) Use of long-acting antihistamines and/or systemic glucocorticoids and/or immunosuppressive drugs Rheumatic diseases Active systemic diseases (e.g., tuberculosis, collagenosis, multiple sclerosis, autoimmune diseases, acquired immune deficiency syndrome) Internal diseases that pose a potential risk to study participants during measurements (e.g., coronary heart disease) and/or influence findings Poor posture or abnormalities of the lower extremities Advanced disc degeneration

Design outcomes

Secondary

MeasureTime frame
Spinal degeneration (objective MRI classification osteochondrosis according to Modic, spondyloarthritis according to Fujiwara, disc degeneration according to Pfirrmann, spinal stenosis according to Schizas, hip osteoarthritis, hip dysplasia, muscle status) at T0. Lower back pain (questionnaire: adapt. von Korff pain scale; Von Korff, Ormel, Keefe, & Dworkin, 1992) at T0 Pain grading lower back pain (questionnaire: adapt. von-Korff pain scale; Von Korff, Ormel, Keefe, & Dworkin, 1992) at T0 Impairment due to back pain (Roland-Morris-Disability Scale, Roland & Morris, 1983) at T0 Health-related quality of life (SF36) at T0.

Primary

MeasureTime frame
The clinical parameter used to test the hypotheses is the (physical) compression force of the lower lumbar spine segments.

Countries

Germany

Contacts

Public ContactTheresa Ahnert

Berlin Institute of Health, Charité - Universitätsmedizin BerlinForschungsgruppe - Biomechanik der Wirbelsäule

rueckenstudie@charite.de+49 (0)30-450 659 000

Outcome results

None listed

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