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Effect of dry needling on spasticity in individuals with chronic stroke

Effect of calf muscles dry needling on spasticity,knee and ankle range of motion and function in individuals with chronic stroke: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20091130002793N5
Enrollment
40
Registered
2019-09-10
Start date
2019-04-21
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

spasticity, knee and ankle range of motion and function in individuals with chronic stroke. Spastic hemiplegia

Interventions

Intervention 1: Intervention group:This group will receive rehabilitation exercises (strengthening exercises, PNF pattern and gait training)and stretch of gastrocnemius, soleus and hip adductors muscl

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 6 months after a stroke involving cerebral cortical regions first-ever unilateral stroke ankle dorsi flexor MMAS spasticity score =2 able to ambulate without supportive device

Exclusion criteria

Exclusion criteria: recurrent stroke previous treatment with BTXA in the 6 months preceding the study progressive or severe neurologic diseases, for example, heart conditions, unstable hypertension, fracture, or implants in the lower extremity fear to needles any contraindication for deep dry needling

Design outcomes

Primary

MeasureTime frame
Spasticity. Timepoint: before intervention, 3 weeks after first session, immediately after last session and 1 week after last session. Method of measurement: Modified Modified Ashworth Scale.

Secondary

MeasureTime frame
Knee range of motion. Timepoint: before intervention, 3 weeks after first session, immediately after last session and 1 week after last session. Method of measurement: protractor.;Ankle range of motion. Timepoint: before intervention, 3 weeks after first session, immediately after last session and 1 week after last session. Method of measurement: protractor.;Functional activity. Timepoint: before intervention, 3 weeks after first session, immediately after last session and 1 week after last session. Method of measurement: Timed Up and Go test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahla Zahednejad

Ahvaz University of Medical Sciences

snejad@ajums.ac.ir+98 61 3374 3102

Outcome results

None listed

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