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A 10-Week EMS Program for Chronic Low Back Pain: What Changed, What Didn’t | Study Conducted By: Concordia University, Montreal, Canada Published In: Journal of Functional Morphology and Kinesiology (Switzerland)

Quick Overview

This 10-week randomized controlled trial from Concordia University studied adults with chronic low back pain using two EMS programs twice weekly. While MRI scans showed minimal structural muscle change, symptom improvements were clearly observed. Across the full sample, average low back pain intensity decreased by about 2 points on a 0–10 scale (p < 0.001). Significant improvements were also reported in disability, pain interference, and pain catastrophizing, with the phasic program showing stronger effects for sitting pain and daily-life impact. The evidence suggests EMS was associated with meaningful symptom improvement over time.

We always provide direct links to the original research at the end of every article so you can review the evidence yourself.


Introduction: Why the ORIEMS FIT Research Digest Exists

ORIEMS FIT Research Digest exists to make real scientific research easier to understand.

We read published university studies.
We translate them into simple language.
We remove hype.
We avoid exaggerated claims.

This article is for educational purposes only.
It is not medical advice.
It is not a diagnosis.
It is not a treatment recommendation.

Our goal is to help you make calm, informed decisions.


What Is This Study About?

This study examined people with chronic low back pain.

The researchers focused on a deep spinal muscle called the lumbar multifidus.
This muscle plays an important role in stabilising the spine.

The main question was:

Can a 10-week electrical muscle stimulation (EMS) program change this muscle in measurable ways?

Two different stimulation programs were tested on the lower back.

Who Conducted the Study?

The study was conducted in Montreal, Canada, within a university health and human performance research setting.

What Type of Electrical Stimulation Was Used?

The device delivered medium-frequency interferential current (IFC).
This type of stimulation is designed to stimulate muscles.

Simple clarification:

  • EMS / NMES: Aims to trigger muscle contractions.

  • TENS: Typically targets sensory nerves and is commonly used for comfort signals.

This study used muscle-focused stimulation, not classic TENS.

Who Was Studied?

Participants were adults aged 18 to 60 with chronic non-specific low back pain lasting more than 3 months.


How Did They Study It?

Number of Participants

  • 35 participants were recruited.

  • 28 completed the full 10-week program.

Study Design

This was a randomised controlled trial (RCT) with two active groups.

Participants were randomly assigned to one of two stimulation programs.

There was no non-stimulation control group.
The study compared two EMS approaches to each other.

Duration

  • 10 weeks

  • 2 sessions per week

Protocol Details

All participants used the same stimulation system applied to the lower back.

Session length increased over time:

  • Weeks 1–3: 20 minutes

  • Weeks 4–6: 25 minutes

  • Weeks 7–10: 30 minutes

Two programs were compared:

Phasic Program

  • 3 kHz carrier frequency

  • 50 Hz modulation

Combined Program

  • 3 kHz carrier frequency

  • 4 Hz and 50 Hz modulation

Intensity was increased until a strong but comfortable muscle contraction was felt.

Measurements Used

The researchers used both imaging and symptom-based measures.

Muscle-focused measures:

  • MRI scans for muscle size and fat infiltration

  • Ultrasound for muscle thickness during contraction

  • Ultrasound elastography for muscle stiffness

Symptom and function measures:

  • Pain ratings (0–10 scale)

  • Disability scores

  • Pain interference scores

  • Pain catastrophising scores


What Did They Find?

The results showed a clear pattern.

1. Muscle Structure Changes Were Mostly Minimal

Most MRI and ultrasound measurements did not show major changes after 10 weeks.

One positive imaging finding was observed:

  • The combined group showed a reduction in fat infiltration at one spinal level on one side (Left L5–S1).

However:

  • This was not a broad structural change.

  • It was isolated to one location.

Overall, the imaging results were mostly neutral.

2. Pain and Daily-Life Scores Improved Over Time

Even though structural muscle changes were limited, participants reported improvements over the 10 weeks.

Improvements were observed in:

  • Pain levels

  • Pain while sitting

  • Pain during movement

  • Disability scores

  • Pain interference

  • Pain catastrophising

The phasic program showed stronger improvement for:

  • Pain while sitting

  • Pain interference

In simple terms:

The muscle scans did not show dramatic rebuilding.
But people reported that pain affected them less and daily life felt easier.


What Does This Mean for Someone Considering EMS?

Safety

This was a supervised clinical study.
It excluded individuals with higher-risk conditions.

If you have:

  • An implanted medical device

  • Heart rhythm conditions

  • Epilepsy

  • Pregnancy

  • Severe or worsening symptoms

You should consult a qualified health professional before using electrical stimulation.

Mechanism of Action (Simple Explanation)

EMS sends electrical impulses that trigger muscle contractions.
This can provide repeated stimulation to a muscle, even if voluntary activation is difficult.

Realistic Expectations

This study does not support dramatic promises like:
“EMS will rebuild deep back muscles quickly.”

Most structural muscle measures did not clearly change in 10 weeks.

What was observed:

  • Improvements in pain-related and daily-life scores.

Who It May Suit

This type of program may suit people who:

  • Want a structured weekly routine

  • Prefer strong but comfortable stimulation

  • Focus on functional improvement rather than visible muscle change

Who Should Seek Professional Advice First

Consult a health professional before starting EMS if you:

  • Have a medical condition

  • Have implanted electronic devices

  • Are pregnant

  • Have seizure history

  • Have heart conditions

  • Have unexplained or worsening pain


What Does This Mean for Someone Already Using EMS?

Consistency Matters

Participants completed 20 sessions over 10 weeks.
Occasional use is not comparable to this structure.

Proper Use Matters

Intensity was adjusted to a strong but comfortable level.
Comfort supports long-term consistency.

Realistic Timelines

In this study:

  • Symptom improvements were clearer than structural muscle changes.

So progress may look like:

  • Sitting feels easier.

  • Daily tasks feel less disrupted.

  • Pain feels less overwhelming.

Rather than:

  • “My deep muscle visibly grew.”

EMS vs TENS Reminder

  • EMS/NMES: Focused on muscle contraction.

  • TENS: Primarily sensory stimulation.

This study used muscle-focused stimulation.


Conclusion

This 10-week randomised trial compared two EMS programs for chronic low back pain.

Most muscle imaging measures showed minimal change.
However, improvements were observed in pain and daily-life impact scores.

This supports a balanced view:

EMS may contribute to improved function and comfort over time.
It should not be viewed as a rapid structural muscle rebuilding tool.

If you want the full technical details, read the original study listed below.


Detailed Research Summary Table

Field Details
Full Study Title The Effect of a 10-Week Electromyostimulation Intervention with the StimaWELL 120MTRS System on Multifidus Morphology and Function in Chronic Low Back Pain Patients: A Randomized Controlled Trial
Authors Daniel Wolfe; Brent Rosenstein; Geoffrey Dover; Mathieu Boily; Maryse Fortin
Year Published 2025
Journal Name Journal of Functional Morphology and Kinesiology
Publisher MDPI
Country of Journal Switzerland
Country of Research Canada
University / Research Centre Concordia University; McGill University Health Centre
DOI Link https://doi.org/10.3390/jfmk10040443
Direct Link to Original Study https://mdpi-res.com/jfmk/jfmk-10-00443/article_deploy/jfmk-10-00443-v2.pdf?version=1764146662
Study Type Randomised Controlled Trial (Two Active Arms)
Number of Participants (Recruited) 35
Number of Participants (Completed) 28
Age Range 18–60
Gender Breakdown Combined: 4 Male, 9 Female; Phasic: 7 Male, 8 Female
Health Condition Studied Chronic Non-Specific Low Back Pain (>3 Months)
Type of Electrical Stimulation EMS Using Medium-Frequency Interferential Current (IFC)
Stimulation Parameters 3 kHz Carrier; 50 Hz (Phasic) or 4 Hz + 50 Hz (Combined); Strong but Comfortable Intensity
Intervention Duration 10 Weeks; 2 Sessions per Week
Session Duration 20–30 Minutes (Progressive)
Control Group No Sham Group; Comparison Between Two Active Protocols
Primary Outcomes MRI Muscle Size and Fat Infiltration
Secondary Outcomes Ultrasound Thickness; Stiffness; Pain; Disability; Interference; Catastrophising
Statistical Findings Improvements Observed in Patient-Reported Outcomes; Minimal Structural Muscle Changes
Funding Mitacs Accelerate; McGill Radiology Practice Plan
Conflict of Interest Funders Reported No Role in Study Design or Reporting
Key Limitations Small Sample; No Non-Stimulation Control; Imaging Mostly Neutral
Research Conclusion Over 10 Weeks, Structural Changes Were Minimal; Improvements Were Observed in Symptom and Function Scores

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Disclaimer 

This article is provided for educational purposes only.

It is not medical advice.
It is not a diagnosis.
It is not a treatment recommendation.

ORIEMS FIT does not claim that EMS devices cure, treat, prevent, or reverse any medical condition.

Research findings described reflect controlled study conditions and may not apply to all individuals.

Individual results vary.
No outcomes are guaranteed.

Consult a qualified health professional before using electrical stimulation, especially if you have medical conditions, implanted devices, pregnancy, seizure history, or heart conditions.

This article does not replace professional medical care.

ORIEMS FIT is not affiliated with the universities, researchers, or journal mentioned.

Readers are responsible for their own health decisions.

To the maximum extent permitted by law, ORIEMS FIT accepts no liability for misuse of products or misinterpretation of this content.

No reproduction rights are granted for commercial redistribution.

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