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Comparing 2-Hz and 100-Hz Electroacupuncture for Postoperative Musculoskeletal Pain: Protocol for a 2 × 2 Prospective
Jeong Hwan Park1, Hyeong Joon Jun1, Young-Eun Kim1
1Korea Institute of Oriental Medicine, Daejeon, Republic of Korea.
JMIR Research Protocols
|June 16, 2026
Summary
This study compares 2 Hz and 100 Hz electroacupuncture for postoperative musculoskeletal pain. Results will inform optimal stimulation frequencies for future trials investigating electroacupuncture analgesia.
Area of Science:
- Pain Management
- Neuroscience
- Rehabilitation Medicine
Background:
- Postoperative pain significantly impacts recovery and quality of life after musculoskeletal surgery.
- Electroacupuncture is a potential adjunct therapy for pain relief, but optimal parameters remain unclear.
Purpose of the Study:
- To compare the analgesic effects of 2 Hz versus 100 Hz electroacupuncture at ST36 to SP9 acupoints.
- To estimate effect sizes and variability for future definitive trials on electroacupuncture in postoperative pain.
Main Methods:
- A single-center, prospective, randomized crossover trial involving 30 adults with postoperative musculoskeletal pain (NRS ≥ 4).
- Participants received two 15-minute sessions of bilateral ST36 to SP9 electroacupuncture at 2 Hz and 100 Hz, with a minimum 7-day washout period.
- A frequency-masked, active-comparator design was employed, with participants unaware of the stimulation frequency or sequence.
Main Results:
- Primary outcomes include changes in pain Numerical Rating Scale (NRS) scores at 15 minutes and 2 hours post-intervention.
- Secondary outcomes assess pain NRS scores at multiple time points, pain characteristics, and physiological measures (pulse rate variability, radial pulse tonometry, activity metrics).
- Recruitment began September 2025, with data collection concluding August 2026 and analysis in late 2026.
Conclusions:
- This trial protocol aims to provide crucial data on the relative analgesic responses to different electroacupuncture frequencies.
- The findings will guide the optimization of stimulation parameters and outcome measures for larger efficacy studies.
- This study does not include a sham or no-treatment control, thus it will not determine absolute efficacy or placebo effects.
