Electrical Stimulation With Interferential Current in the Non-especific Chronic Low Back Pain: Effects on the Autonomic Nervous System.

The aim of this study it's to analyze the relationship between autonomic nervous system balance (ANSb) and chronic pain conditions, especially in this case, non-especific chronic low back pain (CLBP).

Most of physiotherapy approaches focus only in biomechanical aspects, leaving aside what kind of factors could perpetuate CLBP. Since 1985, ANSb was studied due to its potential contribution to chronic pain.

Electrical stimulation, through interferential currents (IFC), it's a safe and well-known therapy used in CLBP with good outcomes regarding pain relief.

The main objective of this study it's to quantify the association between CLBP and ANSb alterations. In second place, the research team aims to record the influence of IFC over pain and ANSb in those subjects.

Study Overview

• Status: Completed
• Conditions: Chronic Pain; Chronic Low-back Pain; Autonomic Imbalance
• Intervention / Treatment: Device: Electrical stimulation: Interferential Current (IFC): Control Group; Device: Electrical stimulation: Interferential Current (IFC): Experimental Group

Detailed Description

In the first place, a meeting will be organized with the patients to resolve any doubt about the study and its process. The investigators will make sure every instruction is understandable, giving enough time to read and ask pertinent questions.

Secondly, patients will be provided of an informed consent specific for the present study, according to the legal forms. Participants must agree with all the information and sign the document.

At this point, patients will be interviewed individually by a researcher to collect all the data regarding to the Clinical History in Physiotherapy.

In the next step, patients will be randomized into two different groups by choosing one opaque envelope, containing a number for the allocation. A researcher will make the final allocation depending on the number. Patients were unaware of the group allocation for masking.

This study has to possible groups with a common indication for both:

1. Experimental group: Patients allocated in this group will receive one single session of interferential current (IFC). Current used a carrier frequency of 4.000 Hz, 65Hz of amplitude modulated frequency (AMF) with sweep frecuency of 95Hz in a 1:1 swing pattern (quadripolar technique). Intensity was adjusted according to patient's tolerance without visible muscle twitches. The session will last 25 min.
2. Control group: This group will receive the same intervention than experimental one but with no intensity, for 25 minutes. Patients will keep his general practitioner's indications about pharmacology.
3. Common indication: Both groups will get instructions to perform a set of home-based exercises for core strengthening after variable collecting.

Before and after the session, all the variable measurements will be collected in the same environmental conditions by the same researcher. Basal measurement (before intervention) will be recorded 15 minutes before session for 10 minutes. The second measurement will be taken while the patient recieves the intervention for 20 minutes.

• Study Type: Interventional
• Enrollment (Actual): 56
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Spain
  • Sevilla, Spain
    • Manuel Albornoz Cabello

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 65 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Male

Description

Inclusion Criteria:

• Subjects diagnosed with cronic low back pain with at least 3 months of evolution.
• Subjects with a minimal pain of 3/10 according to NPRS
• Subjects with informed consent read and signed.
• Subjects not undergoing any other physical therapy intervention.

Exclusion Criteria:

• Any uncontrolled neurological or cardiac disorder.
• Personal Psychological Apprehension Scale (PPAS) score higher than 37.5.
• Contraindication for electrical stimulation.
• Any regular use of medications known to affect the function of the autonomic nervous system (ANS) or pain perception, including antidepressant, benzodiazepines, anti-inflammatory drugs and beta-blockers, 2 weeks before participating in this study.
• Ineligibility to participate determined by the researches.
• Neurological, musculoskeletal or sensory affectations.
• Evidence of infectious process, fever or hypotension.
• Metallic implants in low back area or treated area
• No surgical interventions in low back area
• Not being under pharmacological treatment with influence in Autonomic Nervous System like antidepressants.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Basic Science
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Sham Comparator: Sham IFC therapy: Control group; This group will recieve also instructions for core strengthening exercises and a single session of interferential current (IFC). IFC parameters: Carrier frequency of 4000 Hz; Amplitude modulated frequency of 65 Hz (AMF); Sweep frequency of 95 Hz of modulation with a 1:1 swing pattern, in a quadripolar technique.; NO intensity (0 mA); Session duration: 25 minutes	Device: Electrical stimulation: Interferential Current (IFC): Control Group; Application of IFC with Sonopuls 692® (Enraf-Nonius BV, Rotterdam, The Netherlands) device. Parameters: Carrier frequency of 4000 Hz; Amplitude modulated frequency of 65 Hz (AMF); Sweep frequency of 95 Hz of modulation with a 1:1 swing pattern, in a quadripolar technique.; NO intensity (0 mA); Session duration: 25 minutes
Experimental: IFC therapy: Experimental group; This group will recieve also instructions for core strengthening exercises and a single session of interferential current (IFC). IFC parameters: Carrier frequency of 4000 Hz; Amplitude modulated frequency of 65 Hz (AMF); Sweep frequency of 95 Hz of modulation with a 1:1 swing pattern, in a quadripolar technique.; Intensity will depend on subjet's tolerance but without generating visible muscle twitches.; Session duration: 25 minutes	Device: Electrical stimulation: Interferential Current (IFC): Experimental Group; Application of IFC with Sonopuls 692® (Enraf-Nonius BV, Rotterdam, The Netherlands) device. Parameters: Carrier frequency of 4000 Hz; Amplitude modulated frequency of 65 Hz (AMF); Sweep frequency of 95 Hz of modulation with a 1:1 swing pattern, in a quadripolar technique.; Intensity will depend on subjet's tolerance but without generate visible muscle twitches.; Session duration: 25 minutes

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Heart Rate variability (HRV-a)	Heart Rate variability (HRV) is measured by calculating mean HR, maximum HR and minimum HR. First Beat Bodyguard2 device will be used to collect HRV.	Evaluation before intervention (basal): 15 minutes before intervention, for 10 minutes.
Heart Rate variability (HRV-b)	Heart Rate variability (HRV) is measured by calculating mean HR, maximum HR and minimum HR. First Beat Bodyguard2 device will be used to collect HRV.	Evaluation during the intervention: For 20 minutes, while the interferential current (intervention) is being applied.
Root-mean-square differences of successive heartbeat intervals (RMSSD-a)	RMSSD it's an indirect indicator of parasympathic nervous system level of activity. First Beat Bodyguard2 device will be used to collect RMSSD.	Evaluation before intervention (basal): 15 minutes before intervention, for 10 minutes.
Root-mean-square differences of successive heartbeat intervals (RMSSD-b)	RMSSD it's an indirect indicator of parasympathic nervous system level of activity. First Beat Bodyguard2 device will be used to collect RMSSD.	Evaluation during the intervention: For 20 minutes, while the interferential current (intervention) is being applied.
Standard Deviation 1 (SD1-a)	SD1 is an indicator of the autonomic nervous balance. First Beat Bodyguard2 device will be used to collect it.	Evaluation before intervention (basal): 15 minutes before intervention, for 10 minutes.
Standard Deviation 1 (SD1-b)	SD1 is an indicator of the autonomic nervous balance. First Beat Bodyguard2 device will be used to collect it.	Evaluation during the intervention: For 20 minutes, while the interferential current (intervention) is being applied.
Standard Deviation 2 (SD2-a)	SD2 is an indicator of the autonomic nervous balance. First Beat Bodyguard2 device will be used to collect it.	Evaluation before intervention (basal): 15 minutes before intervention, for 10 minutes.
Standard Deviation 2 (SD2-b)	SD2 is an indicator of the autonomic nervous balance. First Beat Bodyguard2 device will be used to collect it.	Evaluation during the intervention: For 20 minutes, while the interferential current (intervention) is being applied.s.
Stress Index (SS-a)	SS it's an indicator of sympathetic nervous system level of activation. First Beat Bodyguard2 device will be used to collect SS.	Evaluation before intervention (basal): 15 minutes before intervention, for 10 minutes.
Stress Index (SS-b)	SS it's an indicator of sympathetic nervous system level of activation. First Beat Bodyguard2 device will be used to collect SS.	Evaluation during the intervention: For 20 minutes, while the interferential current (intervention) is being applied.s.
Sympathetic / Parasympathetic Ratio (S/PS Ratio-a)	S/PS Ratio it's an indicator of autonomic nervous system balance. First Beat Bodyguard2 device will be used to collect S/PS Ratio.	Evaluation before intervention (basal): 15 minutes before intervention, for 10 minutes.
Sympathetic / Parasympathetic Ratio (S/PS Ratio-b)	S/PS Ratio it's an indicator of autonomic nervous system balance. First Beat Bodyguard2 device will be used to collect S/PS Ratio.	Evaluation during the intervention: For 20 minutes, while the interferential current (intervention) is being applied.s.
Numeric Pain Rating Scale (NPRS-a)	NPRS it's an scale used to measure with ease, patient's perceived pain with a scoring of 0 (no pain) and 10 (maximum pain).	Evaluation before intervention (basal): 15 minutes before intervention.
Numeric Pain Rating Scale (NPRS-b)	NPRS it's an scale used to measure with ease, patient's perceived pain with a scoring of 0 (no pain) and 10 (maximum pain).	Evaluation immediately after treatment session.

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Roland Morris Questionnaire (RMQ-a)	RMQ it's a questionnaire used to measure an individual level of disability related to low back pain, with a scoring of 0 (no disability at all) and 24 (maximum disability).	Evaluation before intervention (basal): 15 minutes before intervention.
Roland Morris Questionnaire (RMQ-b)	RMQ it's a questionnaire used to measure an individual level of disability related to low back pain, with a scoring of 0 (no disability at all) and 24 (maximum disability).	Evaluation immediately after treatment session.
Scale for Personal Psychological Apprehension (SPPA)	SPPA it's a questionnaire made to measure subject's susceptibility to receive electrical stimulation. A scoring of >45 points indicates that subject shouldnt be treated with electrical therapy.	Evaluation before intervention (basal): 15 minutes before intervention.
Dosimetry achieved with electrical stimulation	Maximal dosimetry reached during the session will be recorded in mA.	Recorded immediately after treatment session.

Collaborators and Investigators

• Sponsor: University of Seville

Study record dates

Study Major Dates

• Study Start (Actual): June 1, 2020
• Primary Completion (Actual): November 1, 2020
• Study Completion (Actual): December 10, 2020

Study Registration Dates

• First Submitted: July 14, 2020
• First Submitted That Met QC Criteria: July 20, 2020
• First Posted (Actual): July 23, 2020

Study Record Updates

• Last Update Posted (Actual): July 2, 2021
• Last Update Submitted That Met QC Criteria: June 30, 2021
• Last Verified: June 1, 2021

More Information

Terms related to this study

• Keywords: chronic low back pain; electrical stimulation; autonomic balance; interferential current
• Additional Relevant MeSH Terms: Pain; Neurologic Manifestations; Back Pain; Low Back Pain; Chronic Pain
• Other Study ID Numbers: CIFSNA2020

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No