Trials / Completed
CompletedNCT01060280
Effectiveness of Group GDS and Individual GDS for Treatment of Low Back Pain in Primary Care
The Effectiveness of the Physiotherapy Techniques Group GDS and Individual GDS for the Treatment of Nonspecific Low Back Pain in Primary Care. A Cluster, Randomized, Controlled Trial.
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 461 (actual)
- Sponsor
- Kovacs Foundation · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
A cluster, randomized, controlled clinical trial, where the hypothesis is that Group GDS and Individual GDS are effective in the treatment of nonspecific low back pain. The clusters will be the participating physiotherapy departments in primary care who treat patients with low back pain. In each physiotherapy department there will be 3 groups: education group, Group GDS and Individual GDS. Patients will be followed for 12 months. Variables will be: demographic,intensity of pain, disability, quality of life, patient satisfaction, medication intake for current episode, non-pharmacologic treatment for current episode, co-morbidity, diagnostic tests, sick leave, and habitual physical activity. The questionnaires to be used are: Roland Morris Disability Questionnaire, PI-NRS, VAS, SF-12 and EQ-5d.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BEHAVIORAL | Education on active management | Routine clinical practice plus education on active management. |
| OTHER | Group GDS physiotherapy | Routine clinical practice (which will be substituted by Group GDS) plus education on active management. |
| OTHER | Individual GDS physiotherapy | Routine clinical practice (except for usual physiotherapy, which is substituted by Group and Individual GDS) plus education on active management. |
Timeline
- Start date
- 2010-05-01
- Primary completion
- 2011-10-01
- Completion
- 2012-09-01
- First posted
- 2010-02-02
- Last updated
- 2014-08-18
Locations
1 site across 1 country: Spain
Source: ClinicalTrials.gov record NCT01060280. Inclusion in this directory is not an endorsement.