Randomized Controlled TrialTreatment: TENS & Electrical StimulationClinical RelevanceDOI
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Study Summary

Background

Myofascial pain syndrome (MPS) of the upper trapezius is a common condition that causes trigger-point–related pain, limited neck movement, and abnormal muscle activation patterns. Up to 85% of people experience myofascial pain at some point in their lives. Transcutaneous electrical nerve stimulation (TENS) is widely used as a noninvasive treatment, but clinicians face uncertainty about which frequency and intensity combinations work best. Low-frequency high-intensity (LFHI) stimulation works through endorphin release and descending pain inhibition, while high-frequency low-intensity (HFLI) stimulation works through the gate control theory by activating large sensory fibers.

Despite both approaches being common in clinical practice, direct comparisons of their effects on pain, movement, and muscle function in MPS patients remain limited.

What They Did

The researchers conducted a randomized controlled trial with 30 adults aged 20–40 years who had chronic upper trapezius MPS with active trigger points. Participants were randomly assigned to either the LFHI group (2–8 pulses per second at 25–30 energy units, strong enough to cause visible but non-painful muscle contractions) or the HFLI group (80 pulses per second at 8–10 energy units, set to a comfortable tingling sensation without visible contraction). Both groups received 20-minute TENS sessions twice daily for five consecutive days, with electrodes placed over the most tender trigger points. Before and after the intervention, the researchers measured pain intensity using a 0–10 numeric rating scale, pressure pain threshold with an algometer, cervical range of motion with a goniometer, upper trapezius muscle tone with a myotonometer, and muscle activation patterns using surface electromyography (sEMG) of the upper trapezius, middle deltoid, and levator scapulae during shoulder abduction.

What They Found

Both TENS protocols produced significant improvements across nearly all measured outcomes. Pain intensity dropped from 4.80 to 1.60 in the LFHI group and from 3.80 to 1.73 in the HFLI group (p < .01 for both), with no difference between groups. Pressure pain threshold increased from 9.40 to 15.74 lbf in the LFHI group and from 7.80 to 15.90 lbf in the HFLI group (p < .01 for both). Cervical range of motion improved significantly in all directions for both groups (p < .01): for example, flexion increased from 42.07° to 49.87° with LFHI and from 41.27° to 47.27° with HFLI.

Upper trapezius muscle tone decreased from 349.54 to 291.21 N/m with LFHI and from 363.74 to 312.63 N/m with HFLI (p < .01 for both). sEMG showed reduced upper trapezius and levator scapulae activity and increased middle deltoid activation in both groups (p < .01). The key difference between protocols emerged in muscle coordination: the deltoid-to-upper trapezius activation ratio increased significantly only in the HFLI group, from 1.06 to 1.22 (p < .05), suggesting better normalization of shoulder muscle recruitment patterns with high-frequency low-intensity stimulation.

What This Means

For patients with upper trapezius myofascial pain, both LFHI and HFLI TENS provide meaningful short-term relief of pain, improved neck mobility, reduced muscle tightness, and better muscle balance. The comparable pain outcomes mean clinicians can choose either approach based on patient comfort and preference. However, the finding that HFLI stimulation uniquely improved the deltoid-to-trapezius activation ratio suggests it may offer superior benefits for restoring normal shoulder movement patterns, which could be particularly important for patients whose pain is linked to muscle imbalance or repetitive overhead activities. The twice-daily, five-day protocol was practical and well-tolerated, supporting TENS as an accessible home or clinic-based intervention.

Because the study was short-term with a small sample, longer studies are needed to confirm whether these benefits persist and whether one protocol proves superior for long-term management of chronic MPS.

50/100
Evidence StrengthModerate
Study Quality
Sample Size
Replication
p < .01
Pain Reduction Significance
15.74
LFHI Post-Treatment PPT (lbf)
1.22
HFLI Post-Treatment DT:UT Ratio
p < .05
DT:UT Ratio Improvement (HFLI only)
Enrolled

30

Randomized
n=15

LFHI

2–8 pps TENS at 25–30 energy units, visible contraction

n=15

HFLI

80 pps TENS at 8–10 energy units, sensory level

Results Comparison

NRS Pain Score (0-10)

score
LFHI Pre4.8 score
LFHI Post1.6 score
HFLI Pre3.8 score
HFLI Post1.73 score

Pressure Pain Threshold (lbf)

lbf
LFHI Pre9.4 lbf
LFHI Post15.74 lbf
HFLI Pre7.8 lbf
HFLI Post15.9 lbf

Key Findings

Both LFHI and HFLI TENS significantly reduced pain intensityHigh

NRS decreased from 4.80 ± 1.42 to 1.60 ± 0.98 (LFHI) and from 3.80 ± 1.32 to 1.73 ± 1.03 (HFLI), p < .01 for both

Pressure pain threshold increased significantly with both protocolsHigh

PPT improved from 9.40 ± 2.72 lbf to 15.74 ± 3.77 lbf (LFHI) and from 7.80 ± 2.53 lbf to 15.90 ± 3.31 lbf (HFLI), p < .01 for both

Cervical range of motion improved in all directions for both groupsMedium

Flexion, extension, lateral flexion, and rotation all increased significantly (p < .01), with no between-group differences

Upper trapezius muscle tone decreased significantlyMedium

Tone reduced from 349.54 ± 49.84 N/m to 291.21 ± 46.53 N/m (LFHI) and from 363.74 ± 46.88 N/m to 312.63 ± 32.70 N/m (HFLI), p < .01

HFLI uniquely improved deltoid-to-upper trapezius activation ratioHigh

DT:UT ratio increased from 1.06 ± 0.24 to 1.22 ± 0.30 in HFLI group (p < .05), but only from 1.02 ± 0.27 to 1.13 ± 0.28 in LFHI group (p > .05)

No significant between-group differences for most outcomesMedium

Both protocols produced comparable clinical benefits for pain, PPT, ROM, and muscle tone

Study Methodology
Study Design
Randomized controlled trial with two parallel groups
Sample Size
30
Duration
5 days intervention, pre-post assessment
Population
Adults aged 20–40 years with chronic upper trapezius MPS and active trigger points
Outcome Measures
Numeric Rating Scale (NRS) · Pressure algometer (PPT) · Goniometer (cervical ROM) · Myotonometer (muscle tone) · Surface EMG (%RVC)

Strengths

  • Randomized controlled design with standardized stimulation protocols
  • Multidimensional outcome assessment including pain, function, and muscle physiology
  • Use of sEMG to evaluate neuromuscular activation patterns beyond simple pain scores

Limitations

  • Small sample size (n=15 per group) limits statistical power and generalizability
  • Short 5-day intervention period without long-term follow-up
  • No control or sham group, preventing assessment of natural history or placebo effects
  • Daily activity and posture were not monitored as potential confounders

Key Takeaways for Patients

What This Means for You

  1. 01Both types of TENS can significantly reduce your neck and shoulder pain from muscle trigger points within 5 days
  2. 02You may need to use the device twice daily for 20 minutes to get the best short-term results
  3. 03The gentler, tingling-type stimulation (high-frequency) may help your shoulder muscles work together better during movement
  4. 04Neither approach was clearly superior for pain relief, so you can choose based on what feels more comfortable
  5. 05Talk to your clinician about whether a longer treatment period might be needed for chronic symptoms

Read the Full Paper

Access the complete peer-reviewed study from International Journal of Precision Engineering and Manufacturing

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