Manual Therapy Plus Capacitive and Resistive Electric Transfer Therapy in Individuals With Chronic Low Back Pain

NCT05680467 | Completed

• 1 other identifier: EC-06/2022
• Study Type: interventional
• Target: 60
• Locations: 1 country
• Sites: 1

Brief Summary

Chronic low back pain is defined as back pain that lasts longer than 12 weeks. The aim of this clinical study is to investigate the efficacy of combining a program of manual techniques with the application of Capacitive and Resistive Electric Transfer (TECAR) therapy to treat chronic low back pain. Sixty adults with chronic low back pain will be randomly divided into three groups of 20 each. In the participants of the first group, a therapeutic protocol of manual soft tissue mobilization in the lumbar region will be applied. To the participants of the second group, the same protocol of manual techniques will be applied in combination with TECAR therapy, which will be applied through a conventional capacitive electrode as well as an antistatic electrode bracelet (making the hand of the physical therapist an antistatic electrode). The third group participants will receive no treatment. Both programs will include six treatments over two weeks. Pain in the last 24 hours with the Numeric Pain Rating Scale (NPRS), functional ability with the Roland-Morris Disability Questionnaire (RMDQ), Pressure Pain Threshold (PPT) in the lumbar region with an algometer, and lumbar flexion range of motion through fingertip-to-floor distance (FFD) test will be evaluated before and after the intervention with a follow-up one month later. For the statistical analysis of the results, a two-factor analysis of variance with repeated measurements will be applied, while the statistical significance index will be set at p \< .05.

Conditions

Chronic Low Back Pain

Keywords

Chronic Low back pain; Manual therapy; Capacitive and Resistive Electric Transfer Therapy

Outcome Measures

Primary Outcomes (4)

• Changes in low back pain intensity with Numeric Pain Rating Scale (NPRS)

  This tool is an eleven-point pain scale numbered from zero to 10. The left end of the scale corresponds to zero and is marked as "No pain", whereas the right end corresponds to 10 and is marked as "Maximum pain". Consequently, a higher value indicates more intense pain (Childs et al, 2005). The examinee is asked to choose an integer that best reflects the intensity of their pain. The NPRS is widely used to measure pain in both clinical practice and research, showing high test-retest reliability and high conceptual construct validity.

  pre-treatment, week: 1, 2, 6

• Changes in Pressure Pain Threshold (PPT) with pressure algometry

  Pressure pain threshold (PPT) is defined as the minimal amount of pressure that produces pain. PPT will be assessed by a digital algometer and will be evaluated bilaterally in the quadratus lumborum muscle, in the sacroiliac joints, and paravertebrally in the L4-L5 intervertebral space. The metal rod of the algometer will be placed vertically on the site and the examiner will apply gradually increasing pressure at a rate of 1Kg/s. PPT is calculated in kg/cm2 (Imamura et al., 2016)

  pre-treatment, week: 1, 2, 6

• Changes in functional capacity with the Greek Version of Roland-Morris Disability Questionnaire (RMDQ)

  The functional ability of the participants will be evaluated with the Greek version of the Roland-Morris questionnaire, which consists of 24 questions related to daily activities that patients often report difficulty performing due to low back pain. Each positive answer earns one point and the final score is calculated by adding all the points. Therefore, the higher the score, the greater the restriction. The Greek version of the questionnaire shows satisfactory reliability and validity (ICC: 0.44-0.92) (Boscainos et al., 2003).

  pre-treatment, week: 1, 2, 6

• Changes in lumbar spine flexion range of motion with the Fingertip-To-Floor Test

  Range of trunk forward flexion will be assessed through the Fingertip-To-Floor Test. When performing the test, the examinee is asked to try to reach the ground with the fingers of their hands by leaning forward while keeping their knees and hips extended. The examiner measures with a tape the distance of the fingers from the ground. The test is widely used in clinical practice to measure spinal mobility and shows high reliability and validity indices (Ekedahl et al. 2010).

  Time Frame: pre-treatment, week: 1, 2, 6

Study Arms (3)

"Soft Tissue Mobilization"

EXPERIMENTAL

Participants allocated to this group will receive six sessions of soft tissue mobilization technique accord to Kaltenborn (2018) .

Other: Manual Therapy

"Soft Tissue Mobilization" and "TECAR"

EXPERIMENTAL

Participants allocated to this group will receive the same manual therapy protocol with Group 1 in combination with Capacitive and Resistive Electric Transfer Therapy (TECAR).

Other: Manual Therapy plus TECAR

"Control"

ACTIVE COMPARATOR

Control Group

Other: Control

Interventions

Manual Therapy OTHER

The protocol will last 30 minutes and will include the application of the following manual techniques: * Lumbar soft tissue and joint cranial and lateral mobilization with the patient in the supine position * Bilateral medial lumbar soft tissue mobilization * Functional massage on the quadratus lumborum muscle with the patient in a lateral position on both sides * Extension with coupled sidebending mobilization of the thoracic area with the patient in a lateral position on both sides * Soft tissue lateral mobilization of the thoracic area with the patient in a lateral position on both sides

"Soft Tissue Mobilization"

Manual Therapy plus TECAR OTHER

The participants of this group will be given the same manual protocol as the first group in combination with the application of high frequency current. Soft tissue mobilization manipulations will be applied in combination with a capacitive conventional electrode and with a special electrode bracelet that makes the therapist's own hand as an antistatic electrode. The frequencies of the high frequency current will be 300khz, 500khz, and 1MHz, while as a reference electrode a flexible self-adhesive ground will be used placed on the abdomen

"Soft Tissue Mobilization" and "TECAR"

Control OTHER

Participants in this group will only receive general instructions about managing their back pain and counseling about avoiding activities that may worsen their symptoms.

"Control"

Eligibility Criteria

• Age: 20 Years - 60 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• Duration of symptoms 12 weeks
• Women - Men
• Age range between 20 and 60 years
• Written consent to participate in the study

You may not qualify if:

• Neuropathic pain extending along the lower limb due to nerve root compression
• Previous spine surgery
• History of spine trauma or fracture
• Implanted pacemakers
• Pregnancy
• Cancer
• Systemic musculoskeletal diseases, diagnosed neurodegenerative diseases (e.g., Parkinson's), epilepsy, and history of psychiatric disorders

Sponsors & Collaborators

• International Hellenic University: lead

Study Sites (1)

Department of Physiotherapy, Faculty of Health Sciences International Hellenic Universit

Thessaloniki, Sindos Thessaloníki, 57400, Greece

Location

MeSH Terms

Interventions

Musculoskeletal Manipulations

Intervention Hierarchy (Ancestors)

Complementary Therapies; Therapeutics; Physical Therapy Modalities; Rehabilitation

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: OUTCOMES ASSESSOR
• Masking Details: A masked assessor will conduct the measurements
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Dimitrios Lytras, Principal Investigator, Senior Lecturer of Physiotherapy

Model Details: Sixty participants with chronic low back pain will be randomly assigned to three groups of 20 each. The allocation of the sample to the groups will be performed using a randomization program (https://www.randomizer.org/) by an independent researcher. In the first group, a manual protocol will be applied with the simultaneous application of a high-frequency current through TECAR, in the second group, the same manual protocol will be applied without the TECAR device, while the third group will not receive any treatment. Participants of the two intervention groups will follow a total of six treatments over a period of three weeks with a follow-up after one month.

Study Record Dates

• First Submitted: December 24, 2022
• First Posted: January 11, 2023
• Study Start: December 15, 2022
• Primary Completion: March 15, 2023
• Study Completion: March 15, 2023
• Last Updated: March 28, 2023

Record last verified: 2023-03

Data Sharing

• IPD Sharing: Will not share

Locations

GR (1)