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study of the effects of dry needling with and without intramuscular electrical stimulation on shoulder pain

study of the effects of a single session dry needling with and without intramuscular electrical stimulation on active trigger point in patients with shoulder impingement syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180410039256N1
Enrollment
30
Registered
2018-12-09
Start date
2018-10-22
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

shoulder impingement syndrome. Impingement syndrome of shoulder

Interventions

Intervention 1: Intervention group: dry needling. Intervention 2: Intervention group: dry needling with intramuscular electrical stimulation.

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: patients with shoulder impingement syndrome who have 3 positive tests among neer, hawkins kennedy, jobe,external rotation resistance, painful arc age between 18 to 50 presence of active trigger points in upper trapezius and infraspinatus muscles moderate pain intensity of 3 baised on VAS

Exclusion criteria

Exclusion criteria: any postural disorders like scoliosis ect frozen shoulder any other musculoskeletal disease like myopathy, neck and shoulder surgery etc neurological disease malignancy absolute and relative contraindication use of dry needling for women being on period time

Design outcomes

Primary

MeasureTime frame
Intensity of pain. Timepoint: before the intervention, immediately after the intervention, one week after treatment. Method of measurement: Visual Analogue Scale.;Active shoulder range of motion. Timepoint: before the intervention, immediately after the intervention, one week after treatment. Method of measurement: Goniometery.;Pain pressure threshold. Timepoint: before the intervention, immediately after the intervention, one week after treatment. Method of measurement: digital Algometer.

Secondary

MeasureTime frame
Disability of the arm, shoulder and hand. Timepoint: before the treatment, one week after treatment. Method of measurement: persian version of Disability of the Arm, Shoulder,Hand.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSayena Vahidimanesh

Shahid Beheshti University of Medical Sciences

vahidimanesh1372@sbmu.ac.ir+98 21 2207 7747

Outcome results

None listed

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