Dry Needling vs Electrical Dry Needling for Myofascial Neck Pain
DN-EDN-NP
Comparative Effects of Dry Needling Versus Electrical Dry Needling on Myofascial Trigger Point-Induced Neck Pain, Psychological Distress, and Kinesiophobia
1 other identifier
interventional
34
1 country
1
Brief Summary
Neck pain caused by myofascial trigger points (MTrPs) is common and is associated with pain, psychological distress, and kinesiophobia (fear of movement). This randomized clinical trial compared Dry Needling (DN) and Electrical Dry Needling (EDN), each delivered once weekly for six weeks, in adults with neck pain due to MTrPs. The study measured changes in pain intensity, psychological distress (depression, anxiety, stress), and kinesiophobia before and after treatment, to determine whether adding electrical stimulation to dry needling provides additional benefit over dry needling alone.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 24, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 7, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
August 8, 2026
CompletedFirst Submitted
Initial submission to the registry
August 15, 2026
CompletedFirst Posted
Study publicly available on registry
August 20, 2026
CompletedAugust 20, 2026
August 1, 2026
2 months
August 15, 2026
August 15, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pain Intensity
Measured using the Numeric Pain Rating Scale (NPRS), an 11-point scale where 0 = "no pain" and 10 = "worst pain imaginable".
Baseline (pre-treatment) and Week 6 (post-treatment)
Secondary Outcomes (2)
Psychological Distress
Baseline (pre-treatment) and Week 6 (post-treatment)
Kinesiophobia
Baseline (pre-treatment) and Week 6 (post-treatment)
Study Arms (2)
Group A: Dry Needling
ACTIVE COMPARATORParticipants received Dry Needling using the Hong fast-in/fast-out technique to elicit up to five local twitch responses, followed by ischemic (Travell and Simons) compression over the trigger point until the painful sensation decreased (total \~2 minutes). One session per week for 6 weeks (17 randomized, 16 completed).
Group B: Electrical Dry Needling
EXPERIMENTALParticipants received Electrical Dry Needling: needle insertion into the diagnosed active/latent myofascial trigger point or taut band, followed by application of a low-frequency (2 Hz) continuous biphasic electrical current at a mild-to-moderate intensity for 30 minutes. One session per week for 6 weeks (17 randomized, 16 completed).
Interventions
Stainless-steel acupuncture needles inserted via guide tubes using the Hong technique (rapid insertion/withdrawal in multiple directions) to elicit up to 5 local twitch responses at the active myofascial trigger point, followed by ischemic (Travell and Simons) compression until pain decreased, repeated over several cycles for a total of 2 minutes. One session weekly for 6 weeks.
Needle inserted (after cleaning with sterile alcohol) into the diagnosed active or latent myofascial trigger point/taut band, manipulated bidirectionally to elicit pain/tingling/pressure/heaviness/warmth, then connected to a low-frequency (2 Hz) continuous biphasic electrical current at a mild-to-moderate intensity, left in place for 30 minutes. One session weekly for 6 weeks.
Eligibility Criteria
You may qualify if:
- Adults aged 18-60 years of either gender.
- Neck pain duration ≥ 3 weeks.
- Presence of at least one active myofascial trigger point in the upper trapezius, levator scapulae, SCM, splenius capitis, or scalenes, confirmed using Travell and Simons' criteria.
- Pain intensity ≥ 4 on NPRS (0-10) at baseline.
- Ability to understand and complete questionnaires.
- Willingness to participate and provide written informed consent.
You may not qualify if:
- History of cervical spine trauma, fracture, or surgery.
- Diagnosis of neurological deficits.
- Systemic diseases affecting muscles or joints.
- Use of anticoagulant therapy or bleeding disorders.
- Pregnancy or lactation.
- Active infection or skin lesions in the cervical region.
- Previous dry needling or electrical dry needling treatment in the past 6 months.
- Allergy to needles or local anesthetics if used.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The University of Faisalabad
Faisalābad, Punjab Province, Pakistan
Related Publications (1)
Alghamdi MS, Alghamdi AF, Almalawi AM et al. (2023) The association between neck pain and psychological distress experienced by King Abdulaziz University students: A cross-sectional study. Cureus 15(3): e35685. Brennan K, Elifritz KM, Comire MM et al. (2021) Rate and maintenance of improvement of myofascial pain with dry needling alone vs dry needling with intramuscular electrical stimulation: A randomized controlled trial. The Journal of Manual & Manipulative Therapy 29(4): 216-226. Cagnie B, Danneels L, Van Tiggelen D et al. (2007) Individual and work-related risk factors for neck pain among office workers: A cross-sectional study. European Spine Journal 16(5): 679-686. Hernandez JVL, Calvo-Lobo C, Zugasti AM et al. (2021) Effectiveness of dry needling with percutaneous electrical nerve stimulation of high frequency versus low frequency in patients with myofascial neck pain. Pain Physician 24(2): 135- 143. Lara-Palomo IC, Gil-Martínez E, Antequera-Soler E et al. (2022) Electrical dry needling versus conventional physiotherapy in the treatment of active and latent myofascial trigger points in patients with nonspecific chronic low back pain. Trials 23(1): 238. Moro MZ, De Oliveira Vidal EI, Pinheiro Módolo NS et al. (2024) Dry needling, trigger point electroacupuncture and motor point electroacupuncture for the treatment of myofascial pain syndrome involving the trapezius: A randomized clinical trial. Acupuncture in Medicine 42(1): 3-13. Safran E and Kaya Y (2025) Contextual and placebo effects of suboccipital myofascial release: evaluating its influence on pain threshold, cervical range of motion, and proprioception. BMC Musculoskeletal Disorders 26(1): 502. Umair A, Ghafoor I, Malik S et al. (2024) Effectiveness of manual compression and stretching for the myofascial trigger points in upper trapezius and levator scapulae in office workers. Journal of Health and Rehabilitation Research 4(2): 1301-1306. Valiente-Castrillo P, Martin-Pintado-Zugasti A, Calvo-Lobo C et
BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Dr Muhammad Ateeb, PhD Public Health
The University Of Faisalabad
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 15, 2026
First Posted
August 20, 2026
Study Start
April 24, 2026
Primary Completion
July 7, 2026
Study Completion
August 8, 2026
Last Updated
August 20, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will not share