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Clinical Trials/NCT04115670
NCT04115670
Unknown
Not Applicable

Influence of Health Determinants and Therapeutic Alliance on the Effectiveness of a Pain Neuroscience Education Combined With Motor Control Training With Neurocognitive Focus on Chronic Lumbar Pain in a Population of Professional Caregivers

Fundació Universitària del Bages1 site in 1 country50 target enrollmentDecember 2, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Low-back Pain
Sponsor
Fundació Universitària del Bages
Enrollment
50
Locations
1
Primary Endpoint
Change from Baseline in Pain perceived at 3 months: Visual Analogue Scale
Last Updated
6 years ago

Overview

Brief Summary

Protocols in which pain neuroscience education is combined with physical exercise have shown recently greater effectiveness in the treatment of low back pain in comparison to protocols based only on one of the two approaches. The professional caregiver has a high incidence of low back pain related to the specific aspects of this collection with the low physical condition, the typical tasks performed and other psychosocial aspects. Individual characteristics of these caregivers may condition the effectiveness of the therapy as well as demographic aspects or the alliance between patient and physiotherapist. The aim of this study is to determine the influence of certain health determinants on the effectiveness of a therapy that combines pain neuroscience education and motor control training from a neurocognitive perspective on chronic low back pain in a population of professional caregivers in Bages, analyzing the reduction of low back pain, the improvement of functionality, the reduction of muscle movement and the improvement of muscle coordination.

It will be a quasi-experimental pre-post design, prospective, with a control group, lasting 3 months. The intervention will be performed using a sample of professional caregivers, and the data will be collected before the intervention, at the end of the intervention, and 3-6 months after the intervention. Pain, functionality, conducts of fear/avoidance, and muscular coordination will be analyzed

Registry
clinicaltrials.gov
Start Date
December 2, 2019
End Date
December 20, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Fundació Universitària del Bages
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Of legal age
  • Participants who present lumbar or lumbosacral pain all the time for more than 1 year
  • Score of 6 on the Visual Analogical Scale
  • Have been at work (same position) longer than 1 year

Exclusion Criteria

  • Other alterations and diseases of the musculoskeletal system that may interfere with the results of the intervention.
  • Pregnancy during the study time
  • Older than 65 years old

Outcomes

Primary Outcomes

Change from Baseline in Pain perceived at 3 months: Visual Analogue Scale

Time Frame: Baseline and 3 months

Analisis of pain, using the Visual Analogue Scale, that measure from 0 (no pain) to 10 (excruciating pain)

Change from Baseline in Pain perceived at 6 months: Visual Analogue Scale

Time Frame: Baseline and 6 months

Analisis of pain, using the Visual Analogue Scale, that measure from 0 (no pain) to 10 (excruciating pain)

Secondary Outcomes

  • Change from Baseline in Fear and avoidance of movement at 3 months(Baseline and 3 months)
  • Change from Baseline in Pain disability at 3 months: Oswestry Disability Index(Baseline and 3 months)

Study Sites (1)

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