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The effect of dry needle techniques in the treatment of upper limb patients with stroke

Comparison of the effect of two methods of dry needling application on spasticity, range of motion and upper limb function in patients with chronic stroke: a randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210713051875N1
Enrollment
20
Registered
2021-08-02
Start date
2021-08-11
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Stroke. Brain stem stroke syndrome

Interventions

Intervention 1: Intervention group: Dry needling is performed by fast in fast out technique for the wrist flexor muscles, including the flexor carpi radialis and the flexor carpi ulnaris. Each needle

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: first-ever stroke resulted in hemiplegia disease duration of at least 6 months wrist flexor modified modified Ashworth Scale (MMAS) spasticity score =1 No limitation in passive range of motion of the effected wrist

Exclusion criteria

Exclusion criteria: Any cognitive problems in the patient Diabetes or neurological pain Wrist contracture Dry needling contraindication Taking anti-Spastic drugs

Design outcomes

Primary

MeasureTime frame
Spasticity. Timepoint: Before intervention, immediately after intervention, one week after intervention. Method of measurement: Modified Modified Ashworth.;Function. Timepoint: Before intervention, immediately after intervention, one week after intervention. Method of measurement: Fugle-Meyer assessment upper extremity scale.

Secondary

MeasureTime frame
Active wrist range of motion. Timepoint: Before intervention, immediately after intervention, one week after intervention. Method of measurement: Goniometer.;Passive wrist range of motion. Timepoint: Before intervention, immediately after intervention, one week after intervention. Method of measurement: Goniometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRoshanak Honarpisheh

Tehran University of Medical Sciences

rhonarpisheh@razi.tums.ac.ir+98 21 7752 0174

Outcome results

None listed

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