Status:
COMPLETED
The Effect of Secondary Prevention in Patients With Recurrent Low Back Pain
Lead Sponsor:
University Ghent
Conditions:
Low Back Pain, Recurrent
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
This study investigates the effect of a secondary intervention program for low back pain in patients with recurrent low back pain. One third of the subject will receive no therapy, one third wil recei...
Detailed Description
Participants: 60 individuals with recurrent non-specific LBP were recruited through advertisement in sport facilities, social media and among friends and family. Testing: The testing was performed ...
Eligibility Criteria
Inclusion
- In remission during testing
- recurrent low back pain (RLBP) \>6months
- 2 or more episodes in the past year
- Pain flare of ≥24 hours, characterized by an increase of ≥2 on an Numeric Rating Scale (NRS) scale and/or ≥5 on the Roland Morris Disability Questionnaire
- Followed by a pain-free episode of ≥1 month, characterized by a 0/10 on an NRS scale and/or \<2 on the Roland Morris Disability Questionnaire
- Non-specific RLBP (no cause for Low back pain (LBP); \>3y post discus herniation)
- 1 year or more post-natal
Exclusion
- Use of antidepressants or analgesics (except for NSAIDs or paracetamol), taken 2 weeks before the testing
- Neurologic, respiratory, circulatory, or severe orthopedic diseases
- Pregnancy
- Specific LBP causes
- A history of cognitive exercise therapy and/or specific motor control training
- current treatment or new therapies starting \<6 weeks before baseline assessment
Key Trial Info
Start Date :
September 29 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 30 2020
Estimated Enrollment :
76 Patients enrolled
Trial Details
Trial ID
NCT03852667
Start Date
September 29 2019
End Date
June 30 2020
Last Update
November 30 2021
Active Locations (1)
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1
Vakgroep Revalidatiewetenschappen
Ghent, Oost-Vlaanderen, Belgium, 9000