Neurogenic Bladder Clinical Trial
— TTNS-RCTOfficial title:
Reducing Anticholinergic Bladder Medication Use in Spinal Cord Injury With Home Neuromodulation
Verified date | April 2024 |
Source | The University of Texas Health Science Center, Houston |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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
Status | Completed |
Enrollment | 50 |
Est. completion date | April 20, 2023 |
Est. primary completion date | April 20, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
United States | The University of Texas Health Science Center at Houston | Houston | Texas |
Lead Sponsor | Collaborator |
---|---|
The University of Texas Health Science Center, Houston | National Center for Advancing Translational Sciences (NCATS) |
United States,
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* Note: There are 27 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of Participants With Reduction in Bladder Medication | baseline, 3 months | ||
Primary | Change in Neurogenic Bladder Symptoms (NGB) as Measured by the Neurogenic Bladder Symptom Score (NBSS)Scale. | The Neurogenic Bladder Symptom (NBSS) Score is a questionnaire that measures bladder symptoms. The total score ranges from 0 to 74, a higher score indicating a worse outcome. Scores at baseline are compared to scores at 3 months and reported as categorical. A change within 5 points is stable, = 5 is worse and < 5 is improved. | Baseline, 3 months | |
Primary | Number of Participants With Reduced Neurogenic Bladder Symptoms (NGB) as Measured by the Voiding Diary | baseline, 3 months | ||
Secondary | Change in Quality of Life as Assessed by the I-QOL Questionnaire | The Incontinence Quality of Life questionnaire assesses the impact of urinary incontinence on a person's quality of life. The total score ranges from 0 to 100, a lower score indicating a worse outcome. Scores at baseline are compared to scores at 3 months and reported as categorical. A change within 4 points is stable, = 4 is improved and < 4 is worse | baseline, 3 months | |
Secondary | Number of Participants With Decreased Anticholinergic Side Effects as Measured by the Anticholinergic Side Effects Survey | baseline, 3 months | ||
Secondary | Number of Participants With Increased or Stable Bladder Capacity as Assessed by the Urodynamic Study | baseline, 3 months |
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