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Technology for physiotherapist to identify subgroups in patients with non-specific low back pain.

Technology for physiotherapist to identify subgroups in patients with non-specific low back pain. - Technology for patients with non-specific low back pain.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON45616
Enrollment
200
Registered
2017-03-09
Start date
2017-03-16
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

back complaints low backpain

Interventions

None listed

Sponsors

Saxion, University of Applied Sciences
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients * Between 18 and 65 years old * Acute ( 12 weeks) * Score > 30% points at the Oswestry Disability Index (ODI) * Signed the informed consent form;Healthy subjects * Between 18 and 65 years old * Signed the informed consent form

Exclusion criteria

Exclusion criteria: Patients * Presence of red flags* and lumbarsacral radicular syndrom * Previous backsurgery * Pregnancy or 30;Healthy subjects * non-specific lower back pain * Presence of red flags* and lumbarsacral radicular syndrom * Pregnancy or 30;*Red flags are: Cancer Unexplained weight loss Immunosuppression Prolonged use of steroids Intravenous drug use Urinary tract infection Pain that is increased or unrelieved by rest Fever Significant trauma related to age (e.g., fall from a height or motor vehicle accident in a young patient, minor fall or heavy lifting in a potentially osteoporotic or older patient or a person with possible osteoporosis) Bladder or bowel incontinence Urinary retention (with overflow incontinence) Physical examination Saddle anesthesia Loss of anal sphincter tone Major motor weakness in lower extremities Fever Vertebral tenderness Limited spinal range of motion Neurologic findings persisting beyond one month

Design outcomes

Primary

MeasureTime frame
The primary study parameter are the amount of EMG, with parameters relative rEMG, amplitude (mV), frequency amount(Fmed) in Hz. Range of motion of the trunk by using 3D kinematics and cross-sections and fatty degeneration of the multifidus by using ultrasound.

Secondary

MeasureTime frame
Questionnaires and personal characteristics.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)