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The effect of dry needling on muscle activity pattern and scapulohumeral rhythm in patients with active myofascial trigger points in the upper trapezius muscle

The effect of dry needling on muscle activity pattern and scapulohumeral rhythm in patients with active myofascial trigger points in the upper trapezius muscle

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220314054286N1
Enrollment
22
Registered
2022-04-26
Start date
2022-04-04
Completion date
Unknown
Last updated
2022-05-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with active myofascial trigger point in the upper trapezius muscle.

Interventions

Intervention group: Dry needle( 50 ×0.25) ,The needle is inserted in trigger points perpendicularly. the needle is left in sit for 10 minutes.Dry needling is done totally 5 session, twice a week..

Sponsors

The university of Tarbiat modares
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Individuals have a history of recurrent pain caused by active trigger points of upper trapezius muscle on the dominant side for at least one year. VAS between 1-5

Exclusion criteria

Exclusion criteria: History of cervical trauma in the last 6 months Radiculopathy of cervical History of surgery in the shoulder and the cervical area History of Dry needling in cervical or treatment of MTrP in the last 6 months Needle phobia Severe postural disorder History of epilepsy, depression, migraine, and any mental health disorders Coagulation and vascular diseases based on diagnosis of medical doctor. Any type of orthopedic and neurological disease that affects on position of shoulder, cervical and their function.

Design outcomes

Primary

MeasureTime frame
Muscles activity pattern. Timepoint: Before intervention, 2 days after the end of the intervention session. Method of measurement: Electromyography device.;Scapulohumeral rhythm. Timepoint: Before intervention, 2 days after the end of the intervention session. Method of measurement: Motion analysis device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarid Bahrpeyma

The University of Tarbiat modares

bahrpeyf@modares.ac.ir+98 21 8288 3819

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026