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STEADY; sustained technology for the evaluation of lumbar atrophy and dysfunction*

STEADY; sustained technology for the evaluation of lumbar atrophy and dysfunction* - STEADY;

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON43299
Enrollment
200
Registered
2016-10-25
Start date
Unknown
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

non-specific lower back pain

Interventions

- lumbar artrophy
- multifidus
- technology

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 64 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 * Psychiatric diagnosis * Insufficient knowledge of the Dutch language;Healthy subjects * non-specific lower back pain * Presence of red flags and lumbarsacral radicular syndrom * Pregnancy * Previous backsurgery * Psychiatric diagnosis * Insufficient knowledge of the Dutch language * Body mass index > 30

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
Personal characteristics.

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)