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se of transcranial random noise stimulation (tRNS) as an adjunct to reaching training in chronic stroke survivors with severe arm paresis: An exploratory pilot study.

Not Applicable
Completed
Conditions
Stroke
Physical Medicine / Rehabilitation - Physiotherapy
Stroke - Ischaemic
Stroke - Haemorrhagic
Registration Number
ACTRN12614000952640
Lead Sponsor
Dr Kathryn Hayward
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
8
Inclusion Criteria

All participants will be first time adult (greater than 18 years) stroke survivors who are 6 to 24 months post stroke who demonstrate severe upper limb paresis (as indicated by a Motor Assessment Scale item 6 score of less than 4 out of a possible 6 points). A minimum level of active movement consistent with a triceps brachii score of 2- is required, along with the ability to understand single stage commands. All participants will not have participated in any rehabilitation services for their arm for at least 2-weeks prior to commencement of training.

Exclusion Criteria

Exclusion criteria include: 1) any contraindications to tRNS or MRI, 2) presence of neurological conditions other than stroke e.g., Parkinson’s disease, or upper limb comorbidities that could limit functional recovery e.g., arthritis, 3) elbow contracture greater than 15 degrees, or 4) currently taking medication/s that could alter cortical excitability (e.g., antiepileptic medications, antidepressants) or have a presumed positive or negative effect on neural plasticity (e.g., dopamine, dexamphetamine).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Composite score of Motor Assessment Scale upper limb items 6-8, which measure upper arm function, hand movements and advanced hand movements.[Measured at pre training (week 0), post training (week 4), follow-up (week 12).]
Secondary Outcome Measures
NameTimeMethod
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