Using Telemedicine to Improve Spasticity Diagnosis Rates
Status: | Completed |
---|---|
Conditions: | Neurology, Neurology, Neurology, Neurology |
Therapuetic Areas: | Neurology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 10/11/2018 |
Start Date: | January 30, 2018 |
End Date: | August 1, 2018 |
The purpose of this study is to test the reliability of using telemedicine so a neurologist
can remotely identify residents of a long-term care facility who should be referred to a
neurologist for an in-person spasticity consultation.
can remotely identify residents of a long-term care facility who should be referred to a
neurologist for an in-person spasticity consultation.
The aim of this study is to improve spasticity (a form of muscle rigidity) diagnosis through
validation of telemedicine as a tool for spasticity evaluation or referral. This study will
test the reliability of using telemedicine so a neurologist can remotely identify residents
of a long-term care facility who should be referred to a neurologist for an in-person
spasticity consultation. The telemedicine referral tool will be tested for bedside
implementation in all consenting participants residing in Tennessee State Veteran's Home,
which is a long-term care facility in Murfreesboro, TN. Each of the 140 residents will
receive one neurological examination and one physical examination guided by the
teleneurologist. A medical record review will also be performed.
validation of telemedicine as a tool for spasticity evaluation or referral. This study will
test the reliability of using telemedicine so a neurologist can remotely identify residents
of a long-term care facility who should be referred to a neurologist for an in-person
spasticity consultation. The telemedicine referral tool will be tested for bedside
implementation in all consenting participants residing in Tennessee State Veteran's Home,
which is a long-term care facility in Murfreesboro, TN. Each of the 140 residents will
receive one neurological examination and one physical examination guided by the
teleneurologist. A medical record review will also be performed.
Inclusion Criteria:
- Male or female subjects of any race, aged 18 and above
- Resident of the selected long-term care facility
- The subject, or if appropriate their medical decision maker, is willing and able to
provide written informed consent.
Exclusion Criteria:
- Subjects for whom participation in the study may cause medical harm
We found this trial at
1
site
345 Compton Road
Murfreesboro, Tennessee 37130
Murfreesboro, Tennessee 37130
Principal Investigator: David Charles, M.D.
Phone: 615-895-8850
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