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Effect of Sensory Retraining in Chronic Stroke Patients

Phase 2
Conditions
Stroke.
Stroke, not specified as haemorrhage or infarction
Registration Number
IRCT2017082617301N4
Lead Sponsor
Vice Chancellor for Research, Iran university of medical sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
5
Inclusion Criteria

Major inclusion criteria: having only one experience of stroke (at least 6 months ago); inability to detect normal sensory threshold (monofilament 2/31) at least in one of median, ulnar or radial innervated areas; no history of other neurological or orthopedic conditions; stage 4 or higher according to Brunnstrom's stages; ability to transfer at least one block of Box and Block test;
Major exclusion criteria: Participants were excluded if they have inappropriate collaboration with the program.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hand Dexterity. Timepoint: On three days interval. Method of measurement: Box and Block Test.;Motor function. Timepoint: On three days interval. Method of measurement: Fugl-Meyer assessment and Motoricity Index.
Secondary Outcome Measures
NameTimeMethod
Sensory function. Timepoint: On three days interval. Method of measurement: Semmes-Weinstein Monofilaments.
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