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Effect of dry needling with exercise therapy on stroke spasticity

Effects of Dry Needling and Exercise Therapy on Post-Stroke Spasticity and Motor Function– A Randomized Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180611040061N1
Enrollment
24
Registered
2020-05-17
Start date
2020-11-20
Completion date
Unknown
Last updated
2022-01-11

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

Conditions

Chronic stroke. Cerebral infarction, unspecified

Interventions

Intervention 1: Intervention group: In the treatment group, patients will receive exercise therapy in addition to dry needle. Immediately after dry needle, patients will do exercises in Structure, Fun

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: Documented diagnosis of stroke by a neurologist At least 6 months have passed since the stroke Age>40 years Being the first time stroke leading to hemiplegia Spasticity greater than one for wrist flexor muscles based on MMAS scale Absence of sensory disorders, bleeding, upper limb malignancies, ulcers and infection Ability to understand therapist and evaluator instructions Full consent to participate in the research

Exclusion criteria

Exclusion criteria: Fear of applying dry needles Having contracture in hand Contraindication for dry needling Other neurological lesions Having Diabetes Any history of treatment with nerve blockers such as botulinum toxin A 6 months prior to inclusion

Design outcomes

Primary

MeasureTime frame
Wrist flexors spasticity. Timepoint: Measurement of Spasticity before and after the intervention (4 weeks after intervention) and 3 weeks after the intervention. Method of measurement: Persian version of Modified Modified Ashworth Scale.;Alpha motor neuron excitability. Timepoint: Before and after intervention (4 weeks after intervention) and 3 weeks after intervention. Method of measurement: Electromyography machine (EMG).

Secondary

MeasureTime frame
Range of motion. Timepoint: Before and after intervention (4 weeks after intervention) and 3 weeks after intervention. Method of measurement: Goniometer.;Motor function. Timepoint: Before and after intervention (4 weeks after intervention) and 3 weeks after intervention. Method of measurement: Study of patients motor function with Fugl-Meyer Scale and Action Research Arm Test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNastaran Ghotbi

Tehran University of Medical Sciences

nghotbi@tums.ac.ir+98 21 7753 5132

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 12, 2026