The impact of lumbar orthosis on disability and pain in chronic low back pain

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0006725

Enrollment

Registered

2021-11-09

Start date

2021-03-17

Completion date

Unknown

Last updated

2021-12-02

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

Conditions

None listed

Interventions

Medical Device : 1) Experimental Group : Conventional therapy (8weeks) + Lumbosacral orthosis 2) Control Group : Only Conventional therapy (8weeks) Both groups received routine physical therapy twice

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Men or women between 20 and 60 yr of age 2) Conservative treatment (transforaminal epidural block or caudal block) for neurological low back pain with radicular pain 3) Episode lasting 1 to 3-mon 4) No contraindications to step I or step II analgesics, NSAID, benzodiazepines and thiocolchicoside. Signing the consent form, which was explained to them ?rst

Exclusion criteria

Exclusion criteria: 1) Patients who have used a lumbar belt during the last 6 mo 2) Patients who have suffered from a low back pain episode during the 6 mo preceding inclusion 3) Patients who had had a spinal operation during the 5 yr preceding inclusion 4) Patients who have secondary low back pain due to an accident at work 5) Patients who have a history of spinal arthrodesis 6) Patients who have an unstabilized or symptomatic, chronic cardiac or respiratory complaint 7) Patients who suffer from low back pain with an in?ammatory, tumoural, or infectious cause 8) Patients with a contraindication to step I or step II analgesics, NSAID, benzodiazepines, and thiocolchicoside 9) Patients who are pregnant Patients whose higher functions do not enable them to properly comprehend the protocol or to reliably record the data 10) Exclusion of patients with a chronic cardiac or respiratory complaint was justi?ed by the theoretical warning of the potential effect of wearing a lumbar belt on the increase in cardio-respiratory load

Design outcomes

Primary

Measure	Time frame
Roland-Morris disability questionnaire(RMDQ);The oswestry disability questionnaire (ODQ)’	—

Secondary

Measure	Time frame
Suface EMG on core muscles;Ultrasonographic study	—

Countries

Korea, Republic of

Contacts

Public ContactJaeHyung Kim

Catholic Kwandong University

rehabkjh@hanmail.net+82-32-290-3112

Outcome results