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Clinical Trials/NCT03100721
NCT03100721
Completed
Not Applicable

Pain Neuroscience Education as a Complement to Physiotherapy in Patients With Chronic Musculoskeletal Pain: a Non-randomized Controlled Trial

University of Malaga1 site in 1 country100 target enrollmentApril 4, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Musculoskeletal Pain
Sponsor
University of Malaga
Enrollment
100
Locations
1
Primary Endpoint
Change from Baseline self-efficacy at 1 and 4 months
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Chronic musculoskeletal pain (CMP) is highly prevalent, disabling and with high socio-economic costs, with many negative effects on quality of life. CMP affects the ability to perform work, social, recreational and domestic tasks by changing the mood and concentration of this population that suffers.

In a study carried out in 2010, 17% of the Spanish population had experienced pain in the last month and according to the severity of symptoms 12% felt severe , 64% moderate and 24% mild pain. In this same study it is specified that 61% was due to back pain, 29% due to neck pain and 23% due to shoulder pain.

Pain neuroscience education (PNE) has been shown as an effective treatment strategy in increasing knowledge and understanding of neurobiology, neurophysiology and pain processing, modifying beliefs about it, improving patient skills and encouraging to the accomplishment of physical and social activities in different chronic pathologies.

Detailed Description

Study design and setting: The design of the present study will be a quasi-experimental study with 2 follow-ups (one month and four months after intervention) that will be performed between Apr 2018 and Apr 2020 in public health system in Malaga, Spain. The outcomes will be assessed at baseline (t0), one month (t1) and four months after the physiotherapy treatment begins (t2). Written informed consent will be acquired for all participants prior to their participation.

Registry
clinicaltrials.gov
Start Date
April 4, 2018
End Date
January 22, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Alejandro Luque-Suarez

PhD

University of Malaga

Eligibility Criteria

Inclusion Criteria

  • Age between 18-65 years
  • Chronic Musculoskeletal Pain according to the ACCTION-APS Pain Taxonomy (AAPT), included chronic axial musculoskeletal low back pain

Exclusion Criteria

  • Chronic postoperative musculoskeletal pain and chronic musculoskeletal pain related to a traumatic injury six months before the beginning of the trial
  • Inability to provide written informed consent and/or complete questionnaires in Spanish.

Outcomes

Primary Outcomes

Change from Baseline self-efficacy at 1 and 4 months

Time Frame: 1 and 4 months

This outcome will be measured with the Chronic Pain Self-Efficacy Scale

Secondary Outcomes

  • Change from Baseline pain and pain interference at 1 and 4 months(1 and 4 months)
  • Change from Baseline analgesic medication at 1 and 4 months(1 and 4 months)

Study Sites (1)

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