Ignite Creation Date:
2024-06-16 @ 11:48 AM
Last Modification Date:
2024-10-26 @ 3:30 PM
Study NCT ID:
NCT06421558
Status:
RECRUITING
Last Update Posted:
2024-05-20
First Post:
2024-04-08
Brief Title:
Impact of Direct Current Electrical Stimulation on Treatment of Lumbosacral Radiculopathy
Sponsor:
NeuFit - Neurological Fitness and Education
Organization:
NeuFit - Neurological Fitness and Education
Study Overview
Official Title:
Impact of Direct Current Neuromuscular Electrical Stimulation on Physical Therapy Treatment of Lumbosacral Radiculopathy
Status:
RECRUITING
Status Verified Date:
2024-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study will compare two methods of electrical stimulation alternating current and direct current as an adjunctive therapy to treating lumbosacral radiculopathy Both types of electrical stimulation have been used in clinical practice for physical therapy however direct current stimulation is much less common and there is less known about its impact on physical therapy outcomes The aim of this project is to show the efficacy of a novel device the Neubie direct current device compared to traditional TENS unit in clinical physical therapy treatment of radiculopathy Outcomes measured will include pain intensity functional status neurological status electrophysiological changes and patient satisfaction
Detailed Description:
To determine the efficacy of direct current electrical stimulation the Neubie device on long-term symptoms and severity of lumbosacral and thoracic radiculopathy participants will enroll in a 6-week treatment regimen at one of 16 Hands-On Physical Therapy associated clinic sites listed included in application The first session will consist of an intake evaluation session that will include Numeric Pain Scale for pain Oswestry Disability Index questionnaire to assess functional disability Straight Leg Raise Test to address nerve root irritation or compression and Electrophysiological evaluation to determine the nerve function These tests will serve as baseline and a within subject control for the intervention
Participants will then undergo a specialized radiculopathy protocol that includes traditional PT therapy as well as treatment with the Neubie or traditional electrical stimulation both during PT exercises and as additional treatment after sessions Subjects receive an evaluation session that includes Numeric Pain Scale for pain Oswestry Disability Index questionnaire to assess functional disability Straight Leg Raise Test to address nerve root irritation or compression and Electrophysiological evaluation to determine the nerve function
The experimental group subjects follow with 12 sessions of physical therapy over a 6-week period which include 30 min of various physical therapy exercises with the Neubie
The control group subjects follow with 12 sessions of physical therapy over a 6-week period which include a 30-min of various physical therapy exercises with TENS application
At the end of the 12 sessions of treatment subjects receive an evaluation session that includes Numeric Pain Scale for pain Oswestry Disability Index questionnaire to assess functional disability Straight Leg Raise Test to address nerve root irritation or compression Electrophysiological evaluation to determine the nerve function and a patient satisfaction questionnaire to assess patient satisfaction with the treatment Participants will receive 12 treatments over 6 weeks Measurement of these variables will provide both quantitative and qualitative data on the severity of radiculopathy symptoms see Tools for data collection below
If symptoms of radiculopathy are still present at the 6 week assessment participants will have the option to continue treatment for up to an additional 12 sessions over 6 more weeks to a possible maximum of 24 sessions in 12 weeks Participants will receive a final outcome evaluation session that includes Numeric Pain Rating Scale for pain Oswestry Disability Index questionnaire to assess functional disability Straight Leg Raise Test to address nerve root irritation or compression Electrophysiological evaluation to determine the nerve function and a patient satisfaction questionnaire to assess patient satisfaction with the treatment
Participants will then undergo a specialized radiculopathy protocol that includes traditional PT therapy as well as treatment with the Neubie or traditional electrical stimulation both during PT exercises and as additional treatment after sessions Subjects receive an evaluation session that includes Numeric Pain Scale for pain Oswestry Disability Index questionnaire to assess functional disability Straight Leg Raise Test to address nerve root irritation or compression and Electrophysiological evaluation to determine the nerve function
The experimental group subjects follow with 12 sessions of physical therapy over a 6-week period which include 30 min of various physical therapy exercises with the Neubie
The control group subjects follow with 12 sessions of physical therapy over a 6-week period which include a 30-min of various physical therapy exercises with TENS application
At the end of the 12 sessions of treatment subjects receive an evaluation session that includes Numeric Pain Scale for pain Oswestry Disability Index questionnaire to assess functional disability Straight Leg Raise Test to address nerve root irritation or compression Electrophysiological evaluation to determine the nerve function and a patient satisfaction questionnaire to assess patient satisfaction with the treatment Participants will receive 12 treatments over 6 weeks Measurement of these variables will provide both quantitative and qualitative data on the severity of radiculopathy symptoms see Tools for data collection below
If symptoms of radiculopathy are still present at the 6 week assessment participants will have the option to continue treatment for up to an additional 12 sessions over 6 more weeks to a possible maximum of 24 sessions in 12 weeks Participants will receive a final outcome evaluation session that includes Numeric Pain Rating Scale for pain Oswestry Disability Index questionnaire to assess functional disability Straight Leg Raise Test to address nerve root irritation or compression Electrophysiological evaluation to determine the nerve function and a patient satisfaction questionnaire to assess patient satisfaction with the treatment
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
True
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
None