Reducing Anticholinergic Bladder Medication Use in Spinal Cord Injury With Home Neuromodulation

NCT ID: NCT04074616

Last Updated: 2024-10-15

Study Results

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-11-19

Study Completion Date

2023-04-20

Brief Summary

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The purpose of this study is to determine the efficacy of home transcutaneous tibial nerve stimulation (TTNS) in spinal cord injury(SCI) and to determine the impact on quality of life using TTNS at home

Detailed Description

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Conditions

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Chronic Spinal Cord Injury Neurogenic Bladder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

randomized sham-control trial
Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors
The Study is designed to look at the difference in "high dose" group, which will be submotor amperage, compared to "low dose" which will be set to 1 mA. Both groups will need to stimulate the tibial nerve and visualize toe movement, and then decrease to the amperage of either "high dose" or "low dose." Both groups will use the device for 30 minutes, 5 days per week. A urodynamic study will be performed to measure bladder capacity, sensations while filling, and detrusor pressures before starting using the device and one last time at the end of the study.

We are also conducting surveys to describe differences in preferences with using bladder medications versus devices.

Study Groups

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High Dose

Group Type EXPERIMENTAL

High Dose

Intervention Type DEVICE

Electrodes 2 inch by 2 inch will be placed according to anatomic landmarks,with the negative electrode behind the internal malleolus and the positive electrode 10cm superior to the negative electrode, verified with rhythmic flexion of the toes secondary to stimulation of the flexor digitorum and hallicus brevis. The intensity level will be set to the amperage immediately under the threshold for motor contraction. If the patient perceives pain, the intensity will be lowered until comfortable. Stimulation frequency of 10 Hz and pulse width of 200ms in continuous mode will be used.

Control

Low dose TTNS

Group Type OTHER

Low dose

Intervention Type DEVICE

Toe flexion will be attempted, as in the TTNS protocol. Then the stimulation will be reduced to 1 mA for 30 minutes

Interventions

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High Dose

Electrodes 2 inch by 2 inch will be placed according to anatomic landmarks,with the negative electrode behind the internal malleolus and the positive electrode 10cm superior to the negative electrode, verified with rhythmic flexion of the toes secondary to stimulation of the flexor digitorum and hallicus brevis. The intensity level will be set to the amperage immediately under the threshold for motor contraction. If the patient perceives pain, the intensity will be lowered until comfortable. Stimulation frequency of 10 Hz and pulse width of 200ms in continuous mode will be used.

Intervention Type DEVICE

Low dose

Toe flexion will be attempted, as in the TTNS protocol. Then the stimulation will be reduced to 1 mA for 30 minutes

Intervention Type DEVICE

Other Intervention Names

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TTNS stimulation TTNS stimulation

Eligibility Criteria

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Inclusion Criteria

* Traumatic and non-traumatic SCI performing IC
* Up to 2 anticholinergic overactive bladder (OAB) medications
* No changes in OAB medications
* Neurologic level of injury above T10
* English and Spanish speaking

Exclusion Criteria

* Past history of genitourinary diagnoses or surgeries
* History of central nervous system (CNS) disorders and/or peripheral neuropathy
* Pregnancy
* Lower motor neuron bladder
* Concern for tibial nerve pathway injury
* Absence of toe flexion or AD with electric stimulation
* Bladder chemodenervation in past 6 months
* Potential for progressive SCI including neurodegenerative SCI, ALS, cancer myelopathy, Multiple sclerosis, transverse myelitis
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Center for Advancing Translational Sciences (NCATS)

NIH

Sponsor Role collaborator

The University of Texas Health Science Center, Houston

OTHER

Sponsor Role lead

Responsible Party

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Argyrios Stampas, MD

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Argyos Stampas, MD

Role: PRINCIPAL_INVESTIGATOR

UTHealth

Locations

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The University of Texas Health Science Center at Houston

Houston, Texas, United States

Site Status

Countries

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United States

References

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Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan

View Document

Document Type: Informed Consent Form

View Document

Other Identifiers

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KL2TR003168

Identifier Type: NIH

Identifier Source: secondary_id

View Link

HSC-MS-19-0518

Identifier Type: -

Identifier Source: org_study_id

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