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Rehabilitation following lumbar disc surgery

Completed
Conditions
Low back pain post surgery
10028377
Registration Number
NL-OMON41704
Lead Sponsor
Vrije Universiteit Medisch Centrum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
200
Inclusion Criteria

Inclusion Criteria are: patients who underwent a first time, singe level lumbar discectomy and aged between 18-69 years. ;Inclusion criteria for the qualitative part: having received the intervenion in the randomised trial.

Exclusion Criteria

Co-morbidities of the lumbar spine (eg. fractures, carcinoma*s osteoporosis, etc) Also patients with cauda equina syndrome will be excluded. Furthermore patients that are pregnant and patients with general contra-indications for exercise therapy will be excluded.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Primary outcomes are: global perceived recovery (7-point scale), functional<br /><br>status (Oswestry Disability Index (ODI)), and pain<br /><br>intensity (leg and back) (11-point NRS).<br /><br><br /><br>Qualitative study: factors related to treatment adherence.</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Also general health (SF-36) return to work and quality of life (EuroQol) are<br /><br>measured. Costs will be recorded in cost diaries. Timing of measurement:<br /><br>baseline (in addition to outcomes at baseline also demographics and most<br /><br>important prognostic factors are measured), 3, 6 and 26 weeks.</p><br>
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