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Remote therapeutic effectiveness of dry needling and ischemic pressure on the pain intensity and functional disability of upper limb in patients with myofascial pain syndrome

Remote therapeutic effectiveness of dry needling and ischemic pressure on the pain intensity and functional disability of upper limb in patients with myofascial pain syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200215046499N1
Enrollment
30
Registered
2020-04-07
Start date
2020-05-04
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Myofascial pain syndrome.

Interventions

Intervention 1: Intervention group: Dry needling intervention: In this group, needle enters the active trigger point of the upper trapezius muscle and local twitch response is observed. Then, needle p

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Patient in the age range of 20 to 40 years. Having neck pain or shoulder pain or both of them. The presence of active trigger point in the upper trapezius muscle and latent trigger point in the extensor carpi radialis longus muscle. The intensity of pain should be at least 30 mm on visual analog scale in initial evaluation of active trigger point in the upper trapezius muscle.

Exclusion criteria

Exclusion criteria: History of surgery in the neck or shoulder or upper extremity A history of trauma in the recent years. Radiculopathy in the upper extremity Kyphosis or severe forward head posture Involvement with fibromyalgia syndrome Skin damage, infection, or inflammatory edema in the trigger point region Pregnancy sedative drugs consumption before and during treatment Vascular and coagulation disorders cancer

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: Pre intervention, immediately post treatment, 7 and 14 days after first session. Method of measurement: Visual analogue scale.;Pain pressure threshold. Timepoint: Pre intervention, immediately post treatment, 7 and 14 days after first session. Method of measurement: Algometer.;Disability of the upper limb. Timepoint: before treatment, 7 and 14 days after treatment. Method of measurement: Disability of the Arm Shoulder and Hand (DASH) questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHakimehAdigozali

Tabriz University of Medical Sciences

adigozalih@tbzmed.ac.ir+98 41 3337 5359

Outcome results

None listed

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