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Effectiveness of a sensorimotor treatment program of movement control and sensory discrimination ability in patients with nonspecific chronic low back pain and "control impairment" according to O'Sullivan - a randomized controlled pilot study.

Effectiveness of a sensorimotor treatment program of movement control and sensory discrimination ability in patients with nonspecific chronic low back pain and "control impairment" according to O'Sullivan - a randomized controlled pilot study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00011063
Enrollment
30
Registered
2016-11-11
Start date
2016-09-15
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

nonspecific chronic low back pain with "control impairment" M54.5

Interventions

Group 1: 3 weeks of 3x30-45 minutes of specific training to improve motor control and tactile acuity over 3 weeks (individual training) Group 2: 3 weeks of 3x30-45 minutes of general physical back/cor

Sponsors

Hochschule für Gesundheit Department für angewandte Gesundheitswissenschaften
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: -low back pain (=3month) -= 18 years old -adequate ability to speak and write German -adequate mental ability to give informed consent -intact skin in the area of the low back

Exclusion criteria

Exclusion criteria: -serious diseases/red flags (neoplasm, fracture, acute infection, neurological disease) -current conservative physical therapy treatment or medical pain therapy -acute neurological symptoms (paresthesia, muscle weakness, no reflexes, SLR18) - a physician prohibited to be physical active because of particular diseases -pregnancy - low back pain operation (<1 year)

Design outcomes

Primary

MeasureTime frame
pain intensity and pain interference (BPI=Brief Pain Inventory), physical function (RMDQ=Roland Morris Disability Questionnaire and ODI=Oswestry Disability Index), Quality of life (SF-36=Short Form); assessments are performed 1-2 weeks before intervention, directly before the start of intervention, and after 3 weeks (after intervention is finished)

Secondary

MeasureTime frame
tactile discrimination ability (two-point discrimination threshold), movement control, adverse events, fear-avoidance beliefs (FABQ=Fear-Avoidance Belief Questionnaire); assessments are performed 1-2 weeks before intervention, directly before the start of intervention, and after 3 weeks (after intervention is finished)

Countries

Germany

Contacts

Public ContactChristian Thiel

Hochschule für Gesundheit

christian.thiel@hs-gesundheit.de+49 (0) 234 77727-628

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 25, 2026