Corticospinal and Motor Behavior Responses After Physical Therapy Intervention in Patients With Chronic Low Back Pain.

Low Back Pain Clinical Trial

Official title:

Corticospinal and Motor Behavior Responses After 6-week Transcranial Direct Current Stimulation and Neuromuscular Electrical Stimulation Combined With Motor Control Exercises in Patients With Chronic Low Back Pain

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05156242
• Other study ID #: MU-CIRB 2021/327.2906
• Status: Recruiting
• Phase: N/A
• Start date: September 3, 2021
• Est. completion date: December 31, 2024

Study information

• Verified date: June 2024
• Source: Mahidol University
• Contact: Peemongkon Wattananon
• Phone: 66-2-441-5450
• Email: peemongkon.wat[@]mahidol.ac.th
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study aims to 1) determine the immediate effects of transcranial direct current stimulation (tDCS) on corticospinal excitability, lumbar multifidus muscle (LM) activation, as well as lumbar stability in patients with chronic low back pain (CLBP), 2) determine the immediate effects of neuromuscular electrical stimulation (NMES) on corticospinal excitability, LM activation, as well as lumbar stability in patients with CLBP, 3) compare the effectiveness of 6-week intervention program among tDCS priming with motor control exercise (MCE), NMES priming with MCE, and MCE alone in patients with CLBP, and 4) determine the associations among corticospinal excitability, LM activation, lumbar stability, movement patterns, and clinical outcomes in patients with CLBP.

Description:

This proposed study will use a sample of convenience between the ages of 18 and 40. Subjects who has low back pain more than 3 months or a recurrent pattern of low back pain at least two episodes that interfered with activities of daily living and/or required treatment will be recruited by flyers posted in 2 university physical therapy clinics, as well as word of mouth from subjects and friends. Subjects without a history of low back pain in lifetime will be also recruited to establish normative data. Subjects who are interested in participation will undergo a screening process using inclusion-exclusion criteria checklist and receive brief information regarding the study. If they meet all inclusion criteria, the consent process will be performed.

All subjects will fill out the information sheet for demographic data. Subjects in CLBP will undergo standardized movement system impairment examination and transverse abdominis muscle thickness measurement, self-report questionnaires; pain, disability, quality of life, and fear of movement) and functional tests (5-time sit to stand test, 2-minute step test, functional reach test, prone trunk extension test and abdominal curl test). The project manager responsible for organizing the data collection and blindness will arrange the appointments with the subjects for 2 biomechanical data collection. For the subjects who refuse to participate in biomechanical lab testing, they will proceed to 6-week intervention.

In the first visit (pre-intervention visit#1), biomechanical data including motion and clinical data, lumbar stability, and cortical excitability will be collected. The body landmarks will be identified. These landmarks include 1) lumbar spinous process of T12-S2, 2) lumbar erector spinae (ES) and multifidus (LM) (3 cm lateral to L3 spinous process and 2 cm lateral to L3 spinous process, respectively), 3) bilateral lateral epicondyle of femur, and 4) bilateral lateral malleolus. Spinous process of L1, S2, bilateral lateral epicondyle of femur, and bilateral lateral malleolus will be used as locations for motion tracking sensors, while ES and LM location will be used to place surface electrode for cortical excitability measurement.

For motion and clinical observation data collection, subjects will be instructed to perform 1) sustained positions including usual sitting, corrected position in sitting, usual standing, corrected position in standing, as well as 2) functional movements including active forward bend, stand to sit, sit to stand, walking for 30 seconds, stair ascending, stair descending, and pick up a box from the floor. Then, the subjects will be asked to perform clinical movement tests including active forward bend (waiter's bow), standing with posterior tilt, single leg stance on left and right foot, single leg squat on left and right leg, supine with right and left straight leg raise tests, supine with right and left hip abduction with knee flexion tests, quadruped backward rock test, prone with right and left knee flexion tests, prone with right and left hip internal/external rotation tests, prone with right and left hip extension tests. 1-2 repetitions of practice trial will be provided to familiarize with the movement. Each subject performs 2 sets of 3 consecutive repetitions of each functional movement and clinical movement test in fixed order, while 2 assessors independently rate presence/absence of aberrant movement. Thirty-second rest will be provided between movement tests (rest period can be longer if necessary). Pain intensity, heart rate and rating of perceive exertion (RPE) will be monitored after each test. Motion sensors will be removed.

After that, subjects will undergo lumbar stability test. Two electromagnetic tracking sensors will be placed on T12 and S2 spinous processes, while one sensor will be attached to hand-held dynamometer. Subjects will be asked to position in prone on the treatment bed with both feet on the floor. A researcher will apply 10-kg compression force on L1 to L5 spinous processes for 2 seconds. This 10-kg compression force is derived from the pilot work in which the researchers plotted the graph between compression force in X-axis and posteroanterior displacement in Y-axis. The graph demonstrated plateau (no displacement even increasing in compression force) at approximately 10 kg. Then, subjects will be asked to lift both legs away from the floor presumably activating LM, while the researcher re-apply the same compression force on L1 to L5 again. Pain will be recorded when applying compression force on each spinal level. Sensor displacement will be collected to represent lumbar stability.

For cortical excitability measurement, the subjects will undergo corticospinal excitability measurement using transcranial magnetic stimulation (TMS). The researcher will use ES and LM landmarks for EMG electrode placement. Before placing surface EMG electrodes, the skin will be lightly abraded using abrasive paper and cleaned using cotton with alcohol to lower the skin impedance. Electrodes will be aligned parallel to the muscle fibers. Then, Subjects seat comfortably in a reclined chair with both arms supported. They will be asked to wear a swim cap used to identify stimulation areas for ES and LM. The researcher uses TMS with single-pulse monophasic to stimulate each point over pre-marked scalp sites on a 5 X 7 grid (0-5 cm lateral and from 5 cm anterior to 2 cm posterior to the vertex). Motor cortex stimulation is conducted during submaximal muscle contractions (at 20% MVIC) via EMG visual feedback. Five stimuli will be delivered at each point across the grid with 5-second interval between stimuli and 1-minute rest after each point stimulation. Motor evoke potentials (MEPs) will be recorded. These MEPs will be used to represent corticospinal excitability at baseline. After completion of corticospinal excitability data collection. All electrodes will be removed, and marks on the subject's skin will be erased.

The second visit (pre-intervention visit#2) will be scheduled 1-3 day apart from the first visit (pre-intervention visit#1). Evidence demonstrates the retention of changes in cortical excitability can last for 24 hours; thus, the second visit aims to wash out the effects of TMS on corticospinal excitability from TMS measurement before receiving tDCS or NMES. LM activation measurement at baseline will be collected. The subjects will be in prone position on treatment table with thorax (T3 level) and pelvis (S2 level) securely fastened to the bed. Then, ultrasound transducer will be placed at right L4-5 facet joint by the researcher who is blinded to the group assignment. Right LM thickness at rest will be recorded. After that, the subject will be asked to perform 2 repetitions of maximum voluntary isometric contraction (MVIC) of back extension with rotation to the left to activate right LM with 1-minute rest between repetitions. The researcher will measure right LM thickness during MVIC for both repetitions. Subject will be asked to rate the rating of perceived exertion (RPE) and take 5-minute rest to prevent muscle fatigue. The neuromuscular electrical stimulation (NMES) electrodes will be placed to bilateral LM, and the system will be set at interferential mode (6000 Hz, beat frequency 20-50 Hz, scanning effect). Then, ultrasound transducer will be placed at right L4-5 facet joint by the researcher. The NMES intensity will be set at maximal tolerance to presumably activate most motor units available in the LM. The subject will be asked to perform 2 repetitions of MVIC simultaneously with the NMES.

After LM activation measurement, subjects will be randomly assigned into 3 groups (tDCS priming with MCE group, NMES priming with MCE group, and MCE alone group). For the first visit, we aim to determine the effects of tDCS and NMES against MCE. The subjects in tDCS priming with MCE group will receive the tDCS using 5X7 cm electrodes in which anodal electrode will be placed on M1 representing the back muscles (1 cm anterior and 4 cm lateral to the vertex), while cathodal electrode will be placed on contralateral supraorbital area. The intensity will be set at 2 mA with 10-second fade in/out. The subject will be stimulated by tDCS for 20 minutes. The subjects in NMES priming with MCE group will receive the NMES using interferential mode (6000 Hz, beat frequency 20-50 Hz, scanning effect) on bilateral LM. The intensity will be set at the subject's maximum tolerance. Stimulation will be set at 10 seconds on and 60 seconds off to minimize muscle fatigue. The subjects in MCE group will receive MCE for 20 minutes. After that, all subjects will undergo LM activation, lumbar stability and cortical excitability measurements using the same protocol. These data will be used to determine the immediate effects of tDCS and NMES against MCE (Objective 1 and 3). The researcher will make an appointment with the subjects for 6-week intervention program.

The 6-week intervention program can start at any day based on the subject's preference but should no longer than 1 week after baseline measurement. For 6-week intervention program, the subjects in tDCS priming with MCE group will receive a 20-minute tDCS, while the subjects in NMES priming with MCE group will receive a 20-minute NMES using the same setting as previously mentioned, and the subjects in MCE alone group will receive a 20-minute sham tDCS by setting the intensity at zero mA. After 20 minutes, the subject will receive MCE.

The subject will receive tDCS, sham-tDCS or NMES for 20 minutes followed by 20-minute supervised MCE for every session. The subject is encouraged to perform the same exercise as physical therapy session for 15 minutes once a day and keep record in the exercise logbook. The subject will receive assigned intervention twice a week for 6 weeks. The total number of interventions is 12 sessions. To increase the generalizability of the study, the researchers will not fix the day of the week. The subjects can select any days in the week that is suitable for them. However, we keep twice a week as the evidence shows improvement in pain and disability. Subjects will be asked to fill out pain and disability questionnaires, as well as undergo functional tests at week 2.

After completion of 6-week intervention program, the subjects will undergo biomechanical data collection including motion, clinical observation, LM activation, lumbar stability, and cortical excitability. Clinical outcomes including pain, disability, quality of life, fear of movement, global rating of change, as well as patient's satisfaction will be also collected. Functional tests will be performed after 6-week intervention as well. Baseline and post 6-week data will be used to compare the effectiveness of 6-week intervention program among tDCS priming with MCE, NMES priming with MCE, and MCE alone in patients with CLBP (Objective 3). In addition, corticospinal excitability, LM activation, lumbar stability, movement patterns, and clinical outcomes will be used to determine the associations among parameters (Objective 4).

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 160
• Est. completion date: December 31, 2024
• Est. primary completion date: October 31, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 40 Years

Eligibility

Inclusion Criteria:

The inclusion criteria for individuals without a history of low back pain.

1. Between the ages of 18 and 40

2. No previous history of low back pain in lifetime.

The inclusion criteria for patients with CLBP individuals.

1. Between the ages of 18 and 40.

2. Having low back pain over 3 months or a recurrent pattern of LBP at least two episodes that interfered with activities of daily living and/or required treatment. This information will be obtained by interview during subjective examination.

Exclusion Criteria:

1. History of seizure for either the subject or any family member

2. Implanted pacemaker

3. Clinical signs of systemic disease

4. Definitive neurologic signs including pain, weakness or numbness in the lower extremity

5. Previous spinal surgery

6. Diagnosed osteoporosis, severe spinal stenosis, and/or inflammatory joint disease

7. Any lower extremity condition that would potentially alter trunk movement

8. Vestibular dysfunction

9. Extreme psychosocial involvement

10. Body mass index (BMI) greater than 30 kg/m2

11. Active treatment of another medical illness that would preclude participation in any aspect of the study

12. Menstruation or pregnancy (for female subject)

13. Diagnosed herniated nucleus pulposus (HNP)

14. Contraindications for TMS and tDCS including open wound, infection, lesions, arteriosclerosis, history of haemophilia or demand-type pacemaker

15. Acute cerebral hemorrhage

16. Medications that can interfere the effect of tDCS including sodium channel blocker, calcium channel blocker, NMDA receptor antagonist

Related Conditions & MeSH terms

• Back Pain
• Low Back Pain

Intervention

Device:
• Active-tDCS priming MCE
tDCS is used to enhance cortical excitability before motor control exercises.
• Sham-tDCS priming MCE
tDCS will be set at 0 mA for 20 minutes before motor control exercise.
• NMES priming MCE
NMES is used to enhance lumbar multifidus motor unit recruitment before motor control exercise.

Other:
• Conventional physical therapy
Conventional physical therapy includes modality for pain control, general exercise to improve muscle strength, endurance, and flexibility, and functional training (sit to stand, walking, etc.).

Locations

Country	Name	City	State
Thailand	Faculty of Physical Therapy, Mahidol University	Salaya	Nakhon Pathom

Sponsors (2)

Lead Sponsor	Collaborator
Mahidol University	University of South Carolina

Country where clinical trial is conducted

Thailand, 

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* Note: There are 34 references in all — Click here to view all references

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Corticospinal excitability measurement	Transcranial magnetic stimulation (TMS) will be used to measure corticospinal excitability including resting and active motor thresholds, motor evoke potentials, cortical silent period of LM, and topography (center of gravity coordinate; CoG and volume) of ES and LM, will be primary outcomes for objectives 1-4.	Change from baseline after 1 session and at 6 week after intervention.
Primary	Muscle function measurement	Ultrasound imaging will be used to measure muscle function including TrA and LM thickness, cross-sectional area, and pennation angle will be primary outcome for objective 1-4.	Change from baseline after 1 session and at 6 week after intervention.
Primary	Lumbar stability measurement	Electromagnetic tracking system will be used to measure spinal displacement during applying compression force to represent lumbar stability. This will be primary outcome measures for objective 1-4.	Change from baseline after 1 session and at 6 week after intervention.
Primary	Kinematic measurement	Inertial measurement unit will be used to measure lumbopelvic motions during functional and clinical movement tests. These data can represent movement control. These data will be primary outcome for objectives 3 and 4.	Change from baseline at 6 week after intervention.
Primary	Clinical observation of aberrant movement	Clinician will observe the movements and rate as presence or absence of aberrant movement.	Change from baseline at 6 week after intervention.
Secondary	Self-report questionnaires	self-report questionnaires including pain, disability, quality of life, fear avoidance, global rating of change and patient's satisfaction will be secondary outcomes for objectives 3 and 4. These data will be used to describe subject characteristics and evaluate perception on provided intervention.	Change from baseline at 6 week after intervention.
Secondary	Functional capacity	Functional tests including 5-time sit to stand test (seconds), 2-minute step test (number of steps), functional reach test (centimeters), prone trunk extension test (number of repetitions) and abdominal curl test (number of repetitions) will be secondary outcomes for objectives 3 and 4.	Change from baseline at 6 week after intervention.