Effectiveness of a multidisciplinary intervention in subacute low back pain in the working populatio

Not Applicable

Completed

• Conditions: Subacute low back pain; Musculoskeletal Diseases; Low back pain

• Registration Number: ISRCTN21392091
• Lead Sponsor: a Marató de TV3 Foundation (Fundació La Marató de TV3) (Spain)

Brief Summary

2010 protocol in http://www.ncbi.nlm.nih.gov/pubmed/20067619 2019 results in https://pubmed.ncbi.nlm.nih.gov/31831074/ (added 18/02/2021)

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2008-05-09
• Study Completion: 2011-12-31
• Last Update Posted: 1 March 2021

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 501

Inclusion Criteria

Current information as of 01/02/10:
1. Men and women aged between 18 and 65, who present a current episode of non-specific subacute low back pain, occurs suddenly after a period of a minimum of 6months without LBP and lasts between 15 days and 12 weeks (after ruling out the red flag signs for potentially severe illnesses, listed in the exclusion criteria section)
2. Attended during the study recruiting period
3. Who agree to and sign the informed consent
4. Who understand Catalan or Spanish
5. Who can be accessible for at least twelve months.

Initial information at time of registration:
1. Men and women
2. Aged between 18 and 65
3. Those who present a current episode of non-specific subacute low back pain, the duration of which should last from 15 days to less than 12 weeks (after ruling out the red flag signs for potentially severe illnesses, listed in the exclusion criteria section)
4. Attended during the study recruiting period
5. Who agree to and sign the informed consent
6. Who understand Catalan or Spanish
7. Who remain at the same address for at least six months

Exclusion Criteria

1. Unwillingness to participate in the multidisciplinary intervention trial
2. Pregnancy or breast-feeding mothers
3. Concomitant drug or other substances abuse
4. Anti-inflammatory intolerance or allergy
5. Patients who had treatment for physical problems in the preceding three months and those referred for intensive functional restoration programmes
6. Coexisting cognitive impairment or any other cause of inability to answer the various questionnaires
7. Severe psychiatric disorders: Psychosis, major depression, etc.
8. Presence of red flag signs for potentially severe illnesses

Added 01/02/10:
9. Patients referred for intensive functional restoration programmes
10. Confirmed diagnosis of fibromialgia

Study & Design

• Study Type: Interventional
• Study Design: Not specified