MedTrace Logo

Electrical Stimulation After Botulinum Toxin Injections to the Upper Extremity

NCT04217187 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 28

Last updated 2020-01-07

No results posted yet for this study

Summary

The purpose of this study is to investigate the effectiveness of using electrical stimulation to improve upper extremity function in stroke survivors who receive botulinum toxin injections for spasticity. We hypothesize that individuals who receive the electrical stimulation could demonstrate improved benefit of the botulinum toxin injections and improved functional use of their weaker upper extremity.

Conditions

Interventions

DEVICE

Neuromuscular Electrical Stimulation

Upper extremity neuromuscular electrical stimulation

DEVICE

Sham Electrical Stimulation

Sensory only upper extremity electrical stimulation

Sponsors & Collaborators

  • TIRR Memorial Hermann

    collaborator OTHER

  • Texas Woman's University

    lead OTHER

Principal Investigators

  • Catherine C Hay, PhD · Texas Woman's University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-01-13
Primary Completion
2021-12-31
Completion
2021-12-31
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04217187 on ClinicalTrials.gov