Exploring the impact of Transcutaneous Tibial Nerve Stimulation on quality of life
Qualitative Assessment of the Impact of Transcutaneous Tibial Nerve Stimulation (TTNS) on Quality of Life and Participation
This study looks at how Transcutaneous Tibial Nerve Stimulation affects the daily lives of people with bladder issues to see if it improves their quality of life.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 20 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | Medstar Health Research Institute Academic / other |
| Locations | 1 site (Washington, District of Columbia) |
| Trial ID | NCT04248322 on ClinicalTrials.gov |
What this trial studies
This observational study utilizes semi-structured interviews and focus groups to investigate the experiences of individuals with Neurogenic Lower Urinary Tract Dysfunction who have undergone Transcutaneous Tibial Nerve Stimulation (TTNS). The aim is to identify user-defined themes related to bladder function, catheter-related barriers, and the overall impact on daily life. By gathering qualitative data, the study seeks to enhance understanding of how TTNS affects quality of life and participation in daily activities.
Who should consider this trial
Good fit: Ideal candidates are individuals who have participated in a TTNS study for at least one year.
Not a fit: Patients who have not undergone TTNS or those with conditions unrelated to neurogenic bladder dysfunction may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights that improve treatment approaches for patients with neurogenic bladder issues.
How similar studies have performed: While qualitative assessments of TTNS effects are less common, similar studies exploring patient experiences with neuromodulation have shown promising results.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion: Participated in TTNS Study for 1 year.
Where this trial is running
Washington, District of Columbia
- MedStar National Rehabilitation Hospital — Washington, District of Columbia, United States (Recruiting)
Study contacts
- Principal investigator: Emily Leonard, PhD — Medstar Health Research Institute
- Study coordinator: Emily Leonard, PhD
- Email: emily.m.leonard@medstar.net
- Phone: 202 877-1844
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.