A randomized, double-blinded controlled trial enrolled 60 patients aged 40-65 years with chronic cervical pain. Participants were assigned to receive nociceptor hypostimulation (subthreshold stimulation), hyperstimulation (suprathreshold stimulation), or a sham treatment for 20 minutes, three times per week, over 8 weeks. Outcomes included upper trapezius EMG activity, myofascial trigger point pressure pain threshold, pain intensity, disability, and cervical range of motion.
Post-treatment, the hypostimulation group demonstrated significantly greater improvements across all measured outcomes compared to both the hyperstimulation and control groups (p < 0.05). These improvements in the hypostimulation group were maintained at the 8-week follow-up assessment. In contrast, the hyperstimulation group showed only short-term post-treatment improvements in pain and range of motion, with no improvement in EMG activity, and none of its effects were sustained at follow-up.
Safety, tolerability, and adverse event data were not reported in the abstract. Key limitations include the lack of reported effect sizes, absolute numbers, confidence intervals, and a detailed description of study limitations. The funding source and conflicts of interest were also not reported.
This study provides preliminary evidence from a controlled trial suggesting nociceptor hypostimulation may offer a sustained benefit for chronic cervical pain management compared to hyperstimulation. However, clinicians should interpret these findings cautiously pending publication of the full study report with complete efficacy and safety data.
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BACKGROUND AND PURPOSE: Chronic cervical pain is a common disorder and is difficult to manage. Therefore, this study was conducted to investigate the effects of nociceptor hypostimulation versus hyperstimulation on electromyographic (EMG) activity of cervical muscles, myofascial trigger point (MTP) sensitivity, pain intensity, and disability in patients with chronic cervical pain.
METHODS: Sixty patients with chronic cervical pain were randomly assigned to hypostimulation, hyperstimulation, or control groups. The hypostimulation group received subthreshold stimulation, the hyperstimulation group received suprathreshold stimulation, and the control group received sham treatment. Stimulation was applied for 20 min, three times per week, for 8 weeks. Outcome measures included upper trapezius EMG activity (resting and maximal contraction), pain intensity, MTP pressure pain threshold, and cervical range of motion (flexion, lateral flexion, and rotation bilaterally). Outcomes were assessed at baseline, post-treatment (8 weeks), and follow-up (8 weeks).
RESULTS: At baseline, no significant differences were observed among groups for any outcome (p > 0.05). Post-treatment, the hypostimulation group demonstrated significantly greater improvements than both the hyperstimulation and control groups across all outcomes (p < 0.05). These improvements were maintained at follow-up. Hyperstimulation resulted in short-term improvements in pain and cervical range of motion but not in EMG activity; these effects were not sustained at follow-up.
DISCUSSION: Eight weeks of nociceptor hypostimulation produced significant and sustained improvements in cervical muscle EMG activity, MTP sensitivity, pain, and disability in adults aged 40-65 years with chronic cervical pain. Hypostimulation was superior to hyperstimulation for the long-term management of chronic cervical pain involving upper trapezius MTPs.
TRIAL REGISTRATION: NCT06559358.