Clinical Trials Directory

Trials / Completed

CompletedNCT03913624

Effectiveness of Neuromuscular Electrical Stimulation After Stroke

35 Hz Versus 50 Hz Frequency Stimulation Effects on Motor Recovery in Older Adults After Stroke. A Randomized Clinical Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
69 (actual)
Sponsor
University of Valencia · Academic / Other
Sex
All
Age
60 Years
Healthy volunteers
Not accepted

Summary

A Randomized Clinical Trial (RCT) was conducted to determine the effects of two neuromuscular electrical stimulation protocols with different stimulation frequencies on motor recovery in older adults with spastic hemiparesis after a stroke.

Detailed description

Impairment of the upper limb is one of the most frequent consequences of stroke and directly impacts on the patient's functional status and quality of life. It is estimated that less than 50% of stroke survivors will recover arm function, which will exert a great economic, social and personal toll. Neuromuscular electrical stimulation (NMES) is one of the techniques suggested for upper limb recovery in stroke patients. However, after considering the bibliographic background, more studies are required in order to test its effectiveness, to establish the most efficient NMES protocols and to assess the characteristics of the patients who can benefit the most from this treatment. With this regard, the parameters of the stimulation are currently subject to debate, and more data are needed to optimize the application of this treatment. The aim of this study was to evaluate and compare the effects of two neuromuscular electrical stimulation protocols with different stimulation frequencies on motor impairment, kinaesthetic sensation, functional motor ability, activities of daily living, and quality of life in older adults with spastic hemiparesis suffering a stroke. To cope with the objective of the present study, RCT was conducted. Subjects who met inclusion criteria were recruited from a hospital rehabilitation unit. After the screening and signed consent, participants were randomly allocated to the control group or one of both experimental groups. NMES was applied on wrist and finger extensors for 30 minutes, 3 sessions per week for 8 weeks. The electrostimulation protocols were only differentiated in the parameter of the stimulation frequency, 35 Hz or 50 Hz, depending on the experimental group to which the patient belonged to. Outcome measures were collected at the beginning, after 4 and 8 weeks of treatment, and after a follow-up period (4 weeks).

Conditions

Interventions

TypeNameDescription
OTHERNeuromuscular electrical stimulation

Timeline

Start date
2009-07-01
Primary completion
2014-09-01
Completion
2014-09-01
First posted
2019-04-12
Last updated
2019-04-12

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT03913624. Inclusion in this directory is not an endorsement.