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NCT06341673Recruiting

Impact of TTNS on Bladder Symptoms Among People With MS, A RCT

Impact of Transcutaneous Tibial Nerve Stimulation on Bladder Storage Symptoms and Quality of Life in People With Multiple Sclerosis- A Randomised Controlled Trial"

Source: ClinicalTrials.gov · Last updated 15 May 2026

Brief summary (registry, in English)

Background: Neurogenic lower urinary tract dysfunction is common among people with multiple sclerosis (MS). Recent studies showed that bladder storage symptoms are predominant among MS with a pooled prevalence of frequency at 73.45% followed by urgency at 63.87%. Transcutaneous tibial nerve stimulation (TTNS) is a non-invasive treatment to manage bladder storage symptoms; however, the effectiveness of TTNS is based on a small number of studies with the absence of high-quality evidence. This study aims to investigate the effectiveness of TTNS on bladder storage symptoms compared with sham TTNS among people with MS.Methods: The investigators will use a randomised sham controlled double blind study to explore the effectiveness of TTNS in the treatment of bladder storage symptoms in MS. the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) was followed to standardize the conduct and reporting of the current protocol. The recruitment plan is twofold: 1) Open recruitment for people with MS through King Fahd Hospital of the University communication channels; 2) people with any type of MS attending their routine appointments in MS clinic at King Fahd Hospital of the University, Al Khobar. The investigators will investigate the effectiveness of TTNS compared to sham TTNS on bladder storage symptoms and the effect on quality of life using ICIQ-OAB, ICIQ 3-day bladder diary, ICIQ-LUTS qol, and PSQI. Participant's perception of change post intervention will be evaluated using GPE. Outcomes will be measured at 0, 6 weeks and at 6 months post intervention. A sample size of 72 patients (36 in each group) is required to achieve 90% power with two-tailed tests at an alpha level of 0.05. Conclusion: Multiple sclerosis is a long-term condition, and self-management is important. TTNS provide a safe, non-invasive intervention that can be administered at home. Should the trial determine that TTNS is effective compared to sham TTNS, the investigators will plan to integrate TTNS into standard clinical care pathways in MS.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
72 (estimated)
First submitted
6 Mar 2024
Start date
15 Mar 2024
Primary completion date
28 Nov 2026
Lead sponsor
Hawra Al-Dandan
NCT number
NCT06341673

What you commit to

  • Study type: Interventional
  • Planned participants: 72
  • From 15 Mar 2024 to the primary completion date, 28 Nov 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Recent pelvic related surgery \<1 year

Other illness

  • Bladder malignancy
  • Urinary tract infections (UTIs) during recruitment phase

Other

  • People with MS will be excluded if they have one or more of the following criteria at randomization:
  • Indwelling urethral catheter
  • Indwelling suprapubic catheter
  • Diabetic mellitus
  • Pregnant women or plan to be pregnant during the study intervention
  • Pacemaker or other metallic internal devices
  • Unable to understand the instructions relating to operating the unit
  • Having a bladder BOTOX-injection in the last 12-month

Who the study is looking for

  • Ambulatory (with or without assistive device)
  • Aged ≥18 years old
  • Able to understand spoken and written Arabic Language
  • Self-reported with at least one bladder storage symptom such as urinary frequency urinary urgency, nocturia, with or without urge urinary incontinence
  • Willing to give written informed consent
  • Able to understand how to complete the study outcome measures

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
King Fahd Hospital of the University
Coordinator of this site? Confirm its status
KhobarSaudi ArabiaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.