Pain Neuroscience Education and Physical Exercise Program in Chronic Back Pain
Primary Purpose
Chronic Pain, Musculoskeletal Pain, Back Pain
Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Health Education
Physical exercise
Usual care in Primary Care Physiotherapy Units
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Pain
Eligibility Criteria
Inclusion Criteria:
- Nonspecific back pain of at least 6 months.
- Accept to participate in the study and sign the informed consent.
Exclusion Criteria:
- Oncological pain.
- Spine fracture or surgical intervention in last year.
- Neurological cognitive alteration that prevents understanding the contents of PNE program (In case of doubt, assesment with Minimental test)
- Motor control alteration that prevents the execution of the planned PE program (Minimum requirement: execution in normal time of the Timed Up and Go test)
- Pregnancy.
- Bladder or bowel incontinence.
- Saddle anesthesia.
- Patients presenting other clinical conditions that may aggravate chronic spinal pain (chronic fatigue syndrome, fibromyalgia and complex regional pain syndrome).
- Patients with associated pathologies that make it impossible to perform physical exercise program.
- Patients under treatment with alternative therapies.
Sites / Locations
- Unidad de estrategias de Afrontamiento Activo para el dolor. SacylRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
PNE and PE program
Usual care in Primary Care Physiotherapy
Arm Description
Pain neuroscience education (Health education) and Physical exercise program.
Usual care in Primary Care Physiotherapy Units
Outcomes
Primary Outcome Measures
Change in Health-related Quality of Life at different time points
Medical Outcomes Study 36-Item Short-Form Health Survey (SF-36) V2. Spanish version. The SF-36 is a 36-item scale constructed to survey health status and quality of life. It yields an 8-scale profile of functional health and well-being scores as well as psychometrically-based physical and mental health summary. Each scale is directly transformed into a 0-100 scale. Higher scores indicate better overall quality of life.
Secondary Outcome Measures
Change in Pain assessment at different time points
Visual analog scale (VAS) scale. The VAS is a 100 mm long horizontal line ranging from '0: no pain at all' on one end to '100: worst pain imaginable' on the other end. Participants mark a point along the line that best represents the pain they are experiencing at that moment. A higher score indicates a higher level of pain.
Pressure pain threshold.
Pressure pain threshold (PPT). A digital pressure algometer is used at four standardized points to measure the pressure pain thresholds. Higher values represent a better tolerance to pressure pain.
Change in Pain Catastrophism at different time points
Pain catastrophizing scale (PCS). Spanish version. PCS is a short 13-item measure which evaluates the pain-related catastrophizing behaviours and cognitions of individuals. Score range from 0 - 52. A higher score indicates a higher level of catastrophism.
Change in Kinesiophobia at different time points
Tampa Scale of Kinesiophobia (TSK-11). Spanish version. TSK-11 is a self-report measure that contains 11 questions designed to assess a client's fear of movement and re-injury. Score range from 11 - 44. A higher score indicates a higher level of Kinesiophobia.
Change in Disability at different time points
Roland-Morris Disability Questionnaire (RMDQ). Spanish version. It is a self-administered disability questionnaire consisting of 24 questions that are specifically related to physical functions that may be affected by back pain. Score range from 0 - 24. A higher score indicates a higher level of Disability.
Change in Central sensitization levels at different time points
Central sensitization Inventory (CSI). Spanish version. Self-report instrument to detect the presence of central sensitization. It is a 25-item questionnaire that records the frequency of each symptom on a Likert scale from 0 (never) to 4 (always), resulting in a possible total score of 100. Higher scores are associated with higher levels of central sensitization.
Change in Drugs consumption
Record of consumption by types of drugs. Consumption is evaluated through a survey. The results are expressed in weekly doses per drug type.
Satisfaction survey. Satisfaction with the treatment
Client Satisfaction Questionnaire (CSQ-8). Spanish version. It is is a self-report instrument used to assess satisfaction with health services and it is used to assess participant satisfaction with the treatment. Scores range from 8 - 32. Higher scores are associated with higher satisfaction.
Modifications of body mass index.
modification of the body mass index (BMI). Weight in Kg. and Height ill be combined to report BMI in kg/m^2.
Full Information
NCT ID
NCT03654235
First Posted
August 24, 2018
Last Updated
February 19, 2020
Sponsor
Fundacion para la Investigacion y Formacion en Ciencias de la Salud
Collaborators
Castilla-León Health Service, University of Valladolid
1. Study Identification
Unique Protocol Identification Number
NCT03654235
Brief Title
Pain Neuroscience Education and Physical Exercise Program in Chronic Back Pain
Official Title
Pain Neuroscience Education and Physical Exercise Program in Patients With Chronic Back Pain. Intervention From Primary Care Physiotherapy Units
Study Type
Interventional
2. Study Status
Record Verification Date
February 2020
Overall Recruitment Status
Unknown status
Study Start Date
February 1, 2017 (Actual)
Primary Completion Date
November 30, 2020 (Anticipated)
Study Completion Date
December 30, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fundacion para la Investigacion y Formacion en Ciencias de la Salud
Collaborators
Castilla-León Health Service, University of Valladolid
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study evaluates the effects of a pain neuroscience education (PNE) and physical exercise (PE) program in patients with chronic back pain. Half of participants receive PNE and PE program supervised by a physiotherapist and the other half receive usual physiotherapy care supported by physiotherapy protocols in primary care.
Detailed Description
Justification: Chronic musculoskeletal pain (CMP) affects more than 20% of the population, its prevalence is increasing, generating suffering and high health expenditure. The current knowledge of neurophysiology of pain shows that the painful experience in CMP is not necessarily associated with peripheral tissue damage and is due more to an alteration of central mechanisms of pain processing and to the dysfunction of endogenous pain inhibitory mechanisms. Physical exercise (PE) has been shown to be effective in CMP. Pain neuroscience education (PNE) improves the levels of pain catastrophism, Kinesiophobia, quality of life, disability and also modifies maladaptive cognitions that favour a painful response.
Objectives: To evaluate the efficacy of a PNE and PE in patients with chronic back pain (CBP). Changes in pain intensity, pain thresholds, Catastrophism, kinesiophobia, disability, central sensitization and quality of are measured.
Material and methods: Multicenter randomized clinical trial (RCT) with 170 patients. Intervention group receive 6 sessions of PNE and a 6 weeks PE program (18 sessions) aimed at improving functional capacity, neurogenesis and cerebral plasticity. Control group receive usual physiotherapy treatment (supported by the current protocols in Primary Care in the Health System of Castilla y León). The outcome variables are measured by Visual Analog Scale (EVA), Pressure Pain Threshold (PPT), Kinesiophobia Tampa Scale (TKS-11), Central Sensitization Questionnaire (CSC), Pain Catastrophism Questionnaire (CCD), disability (Roland-Morris), Quality of life (SF-36) and satisfaction (CSQ-8). An initial assessment, post-intervention (week 10), at six months and at year is performed. Patients Evaluator and Outcomes Assessor are masked.
Applicability of results: The proposed intervention is simple and reproducible. It can be performed in the Primary Care Physiotherapy Units. It requires few resources, and it can produce changes in pain intensity, functionality and quality of life of patients with CBP
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Pain, Musculoskeletal Pain, Back Pain
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
Patients Evaluator and Outcomes Assessor are masked
Allocation
Randomized
Enrollment
170 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
PNE and PE program
Arm Type
Experimental
Arm Description
Pain neuroscience education (Health education) and Physical exercise program.
Arm Title
Usual care in Primary Care Physiotherapy
Arm Type
Active Comparator
Arm Description
Usual care in Primary Care Physiotherapy Units
Intervention Type
Other
Intervention Name(s)
Health Education
Intervention Description
6 pain neuroscience education sessions (10 hours) and delivery of printed reinforcement material.
Intervention Type
Other
Intervention Name(s)
Physical exercise
Intervention Description
Group physical exercise program (18 sessions; 3 sessions/week) leaded by a physiotherapist. It includes exercises to improve strength, coordination, balance and aerobic capacity. Work with double tasks, recreational activities to overcome kinesiophobia and activities to do at home are used in the program.
Intervention Type
Other
Intervention Name(s)
Usual care in Primary Care Physiotherapy Units
Intervention Description
Treatment supported by the protocol of primary care of physiotherapy in the health service of Castilla y León that was in force at the time of the intervention.
Patients receive 15 sessions of analgesic electrotherapy, thermotherapy and standardized physical exercise
Primary Outcome Measure Information:
Title
Change in Health-related Quality of Life at different time points
Description
Medical Outcomes Study 36-Item Short-Form Health Survey (SF-36) V2. Spanish version. The SF-36 is a 36-item scale constructed to survey health status and quality of life. It yields an 8-scale profile of functional health and well-being scores as well as psychometrically-based physical and mental health summary. Each scale is directly transformed into a 0-100 scale. Higher scores indicate better overall quality of life.
Time Frame
Change from baseline to post-treatment, to 6 months and at 12 months follow-up
Secondary Outcome Measure Information:
Title
Change in Pain assessment at different time points
Description
Visual analog scale (VAS) scale. The VAS is a 100 mm long horizontal line ranging from '0: no pain at all' on one end to '100: worst pain imaginable' on the other end. Participants mark a point along the line that best represents the pain they are experiencing at that moment. A higher score indicates a higher level of pain.
Time Frame
Change from baseline to post-treatment, to 6 months and at 12 months follow-up
Title
Pressure pain threshold.
Description
Pressure pain threshold (PPT). A digital pressure algometer is used at four standardized points to measure the pressure pain thresholds. Higher values represent a better tolerance to pressure pain.
Time Frame
Change from baseline to post-treatment, to 6 months and at 12 months follow-up
Title
Change in Pain Catastrophism at different time points
Description
Pain catastrophizing scale (PCS). Spanish version. PCS is a short 13-item measure which evaluates the pain-related catastrophizing behaviours and cognitions of individuals. Score range from 0 - 52. A higher score indicates a higher level of catastrophism.
Time Frame
Change from baseline to post-treatment, to 6 months and at 12 months follow-up
Title
Change in Kinesiophobia at different time points
Description
Tampa Scale of Kinesiophobia (TSK-11). Spanish version. TSK-11 is a self-report measure that contains 11 questions designed to assess a client's fear of movement and re-injury. Score range from 11 - 44. A higher score indicates a higher level of Kinesiophobia.
Time Frame
Change from baseline to post-treatment, to 6 months and at 12 months follow-up
Title
Change in Disability at different time points
Description
Roland-Morris Disability Questionnaire (RMDQ). Spanish version. It is a self-administered disability questionnaire consisting of 24 questions that are specifically related to physical functions that may be affected by back pain. Score range from 0 - 24. A higher score indicates a higher level of Disability.
Time Frame
Change from baseline to post-treatment, to 6 months and at 12 months follow-up
Title
Change in Central sensitization levels at different time points
Description
Central sensitization Inventory (CSI). Spanish version. Self-report instrument to detect the presence of central sensitization. It is a 25-item questionnaire that records the frequency of each symptom on a Likert scale from 0 (never) to 4 (always), resulting in a possible total score of 100. Higher scores are associated with higher levels of central sensitization.
Time Frame
Change from baseline to post-treatment, to 6 months and at 12 months follow-up
Title
Change in Drugs consumption
Description
Record of consumption by types of drugs. Consumption is evaluated through a survey. The results are expressed in weekly doses per drug type.
Time Frame
Change from baseline to post-treatment, to 6 months and at 12 months follow-up
Title
Satisfaction survey. Satisfaction with the treatment
Description
Client Satisfaction Questionnaire (CSQ-8). Spanish version. It is is a self-report instrument used to assess satisfaction with health services and it is used to assess participant satisfaction with the treatment. Scores range from 8 - 32. Higher scores are associated with higher satisfaction.
Time Frame
at 10 weeks
Title
Modifications of body mass index.
Description
modification of the body mass index (BMI). Weight in Kg. and Height ill be combined to report BMI in kg/m^2.
Time Frame
Change from baseline to post-treatment, to 6 months and at 12 months follow-up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Nonspecific back pain of at least 6 months.
Accept to participate in the study and sign the informed consent.
Exclusion Criteria:
Oncological pain.
Spine fracture or surgical intervention in last year.
Neurological cognitive alteration that prevents understanding the contents of PNE program (In case of doubt, assesment with Minimental test)
Motor control alteration that prevents the execution of the planned PE program (Minimum requirement: execution in normal time of the Timed Up and Go test)
Pregnancy.
Bladder or bowel incontinence.
Saddle anesthesia.
Patients presenting other clinical conditions that may aggravate chronic spinal pain (chronic fatigue syndrome, fibromyalgia and complex regional pain syndrome).
Patients with associated pathologies that make it impossible to perform physical exercise program.
Patients under treatment with alternative therapies.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Federico Montero Cuadrado
Phone
+34 651529993
Email
fmonteroc@saludcastillayleon.es
First Name & Middle Initial & Last Name or Official Title & Degree
Miguel Á. Galán Martín
Phone
+34 609686744
Email
magalanm@saludcastillayleon.es
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Miguel A. Galán Martín
Organizational Affiliation
Castilla-León Health Service
Official's Role
Principal Investigator
Facility Information:
Facility Name
Unidad de estrategias de Afrontamiento Activo para el dolor. Sacyl
City
Valladolid
ZIP/Postal Code
47011
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Miguel Angel Galán-Martín
Phone
983255400
Ext
88870
Email
magalanm@saludcastillayleon.es
First Name & Middle Initial & Last Name & Degree
Federico Montero Cuadrado
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
31679512
Citation
Galan-Martin MA, Montero-Cuadrado F, Lluch-Girbes E, Coca-Lopez MC, Mayo-Iscar A, Cuesta-Vargas A. Pain neuroscience education and physical exercise for patients with chronic spinal pain in primary healthcare: a randomised trial protocol. BMC Musculoskelet Disord. 2019 Nov 3;20(1):505. doi: 10.1186/s12891-019-2889-1.
Results Reference
derived
Learn more about this trial
Pain Neuroscience Education and Physical Exercise Program in Chronic Back Pain
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