Transcranial Direct Current Stimulation Combined With Exercise in Low Back Pain
Primary Purpose
Low Back Pain, Transcranial Direct Current Stimulation
Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Transcranial direct current stimulation
Sham Transcranial direct current stimulation
Sponsored by
About this trial
This is an interventional treatment trial for Low Back Pain focused on measuring Transcranial Direct Current Stimulation, Low back pain, Exercise, Chronic pain, Combined modality therapy, Motor cortex
Eligibility Criteria
Inclusion Criteria:
- Men and women with chronic nonspecific low back pain (for more than 12 weeks) and minimum pain intensity of 3 on numerical pain rating scale.
Exclusion Criteria:
- diagnosis of fracture and spine pathologies, fibromyalgia, spine surgery in the last year;
- low cognitive level assessed by the Mini Mental State Examination;
- presence of central neurological diseases (such as Parkinson's and stroke) or psychiatric (such as depression or schizophrenia);
- history of epileptic illness;
- seizure history;
- brain implants;
- pacemaker;
- pregnancy.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Sham Comparator
Arm Label
Stimulation + exercise group
Sham stimulation + exercise group
Arm Description
30-minute exercise program (based on Pilates method) combined with active transcranial direct current stimulation.
This arm will perform the same procedures of experimental group but the stimulator will be turned off after 30 seconds and the volunteers will not receive current for the rest of the session.
Outcomes
Primary Outcome Measures
Pain intensity
Pain intensity measured by numerical pain rating scale (11 points scale)
Functional performance associated to back pain
Functional performance associated with low back pain measured by Roland Morris Disability Questionnaire (24 itens)
Secondary Outcome Measures
Pressure pain threshold
Pressure pain threshold measured by pressure algometer.
Individual quality of life
Measurement of quality of life using SF-36 questionnaire (36 items, divided into 8 subscales)
Patient global impression of change
Patient global impression of change measured by a scale with seven points, where 1 is equal to no change or worse and 7 is much better.
Central Sensitization
Evaluation of Central Sensitization using Central Sensitization Inventory (CSI).The questionnaire is divided into two parts, the first with a score from 0 to 100 measures 25 somatic and emotional symptoms, while the second part relates to specific previous diagnoses.
Adverse events
Patient perception of any adverse event during the intervention protocol.
Use of medications
Patient declaration of medication use.
Full Information
NCT ID
NCT05467566
First Posted
July 15, 2022
Last Updated
July 19, 2022
Sponsor
Universidade Federal do Rio Grande do Norte
1. Study Identification
Unique Protocol Identification Number
NCT05467566
Brief Title
Transcranial Direct Current Stimulation Combined With Exercise in Low Back Pain
Official Title
The Effects of Transcranial Direct Current Stimulation Combined With Pilates Based Exercise in the Treatment of Patients With Chronic Low Back Pain
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 2022 (Anticipated)
Primary Completion Date
August 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidade Federal do Rio Grande do Norte
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
The purpose of this study is to evaluate the effects of transcranial direct current stimulation combined with Pilates based exercise on chronic low back pain. This is a randomized clinical trial composed of two arms.
Detailed Description
Chronic low back pain may be associated with pathoanatomical, neurophysiological, physical, psychological and social factors. Treatments that relieve the symptoms of these patients are of great importance to improve the quality of life of these individuals. Thus, this study aims to evaluate the effects of transcranial direct current stimulation combined with Pilates based exercise on chronic low back pain. This is a randomized clinical trial that will be composed of men and women between 18 and 65 years of age, with a history of low back pain for more than 12 weeks and a minimum pain intensity equal to 3 cm on the numerical pain scale. The volunteers will be randomized into two distinct groups: stimulation + exercise group (EG - will perform a Pilates based exercise protocol combined with transcranial direct current stimulation) and sham stimulation + exercise group (SG - will perform the same exercise program combined with sham stimulation). The interventions, regardless of the group, will be carried out three times a week for four weeks. Participants will be submitted to three assessments: the first (T0) will be performed before the treatment protocols; the second (T1) will be performed after the four weeks of intervention; and the third (T2) will be a follow-up one month after the end of the treatment protocol. Pain sensation, functional performance, central sensitization, quality of life, pressure pain threshold, global impression of change, adverse events and medication use will be evaluated. For the statistical analysis, a mixed model ANOVA will be performed for the inter and intragroup comparison, with Tukey's post hoc, considering a significance level of 5%.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Low Back Pain, Transcranial Direct Current Stimulation
Keywords
Transcranial Direct Current Stimulation, Low back pain, Exercise, Chronic pain, Combined modality therapy, Motor cortex
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
42 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Stimulation + exercise group
Arm Type
Experimental
Arm Description
30-minute exercise program (based on Pilates method) combined with active transcranial direct current stimulation.
Arm Title
Sham stimulation + exercise group
Arm Type
Sham Comparator
Arm Description
This arm will perform the same procedures of experimental group but the stimulator will be turned off after 30 seconds and the volunteers will not receive current for the rest of the session.
Intervention Type
Device
Intervention Name(s)
Transcranial direct current stimulation
Intervention Description
Exercise protocol + application of active direct current stimulation for 30 minutes.
Intervention Type
Device
Intervention Name(s)
Sham Transcranial direct current stimulation
Intervention Description
Exercise protocol + application of simulation of direct current stimulation for 30 minutes. The stimulator will be turned off after 30 seconds and the volunteers will not receive current for the rest of the session.
Primary Outcome Measure Information:
Title
Pain intensity
Description
Pain intensity measured by numerical pain rating scale (11 points scale)
Time Frame
Change from baseline in pain intensity at four weeks after intervention and 1 month of follow-up
Title
Functional performance associated to back pain
Description
Functional performance associated with low back pain measured by Roland Morris Disability Questionnaire (24 itens)
Time Frame
Change from baseline in functional performance at four weeks after intervention and 1 month of follow-up
Secondary Outcome Measure Information:
Title
Pressure pain threshold
Description
Pressure pain threshold measured by pressure algometer.
Time Frame
Change from baseline in pressure pain threshold at four weeks after intervention and 1 month of follow-up
Title
Individual quality of life
Description
Measurement of quality of life using SF-36 questionnaire (36 items, divided into 8 subscales)
Time Frame
Change from baseline in quality of life questionnaires at four weeks after intervention and 1 month of follow-up
Title
Patient global impression of change
Description
Patient global impression of change measured by a scale with seven points, where 1 is equal to no change or worse and 7 is much better.
Time Frame
Change from baseline in Patient global impression of change at each intervention day and at four weeks of intervention and 1 month of follow-up.
Title
Central Sensitization
Description
Evaluation of Central Sensitization using Central Sensitization Inventory (CSI).The questionnaire is divided into two parts, the first with a score from 0 to 100 measures 25 somatic and emotional symptoms, while the second part relates to specific previous diagnoses.
Time Frame
Change from baseline of central sensitization at four weeks after intervention and 1 month of follow-up.
Title
Adverse events
Description
Patient perception of any adverse event during the intervention protocol.
Time Frame
Up to 4 weeks of intervention and 1 month of follow-up.
Title
Use of medications
Description
Patient declaration of medication use.
Time Frame
Up to 4 weeks of intervention and 1 month of follow-up.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Men and women with chronic nonspecific low back pain (for more than 12 weeks) and minimum pain intensity of 3 on numerical pain rating scale.
Exclusion Criteria:
diagnosis of fracture and spine pathologies, fibromyalgia, spine surgery in the last year;
low cognitive level assessed by the Mini Mental State Examination;
presence of central neurological diseases (such as Parkinson's and stroke) or psychiatric (such as depression or schizophrenia);
history of epileptic illness;
seizure history;
brain implants;
pacemaker;
pregnancy.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Liane B Macedo, PhD
Phone
+55 (84) 3342-2287
Email
liane.macedo@ufrn.br
12. IPD Sharing Statement
Plan to Share IPD
No
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Transcranial Direct Current Stimulation Combined With Exercise in Low Back Pain
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