search
Back to results

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
Universidade Federal do Rio Grande do Norte
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    July 15, 2022
    Last Updated
    July 19, 2022
    Sponsor
    Universidade Federal do Rio Grande do Norte
    search

    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

    Learn more about this trial

    Transcranial Direct Current Stimulation Combined With Exercise in Low Back Pain

    We'll reach out to this number within 24 hrs