Rehabilitation Program for Bladder Control in Individuals With Incomplete Spinal Cord Injury

Rehabilitation
Bladder health/function
Online since 8 July 2025, updated 155 days ago

About this trial

This prospective, randomized, double-blind clinical trial (with both participants and outcome assessors blinded to group assignments) was carried out at the outpatient clinic of the Faculty of Physica...

Included participants

Gender
Male
Age
18 - 65 years
Injury level
C1 - L1
  • Severity (AIS)?
  • AIS-C
    AIS-D
    Time since injury
    All
    Healthy volunteers
    No
    C1-L1

    What’s involved

    Type

    Rehabilitation

    Details

    This prospective, randomized, double-blind clinical trial (with both participants and outcome assessors blinded to group assignments) was carried out at the outpatient clinic of the Faculty of Physical Therapy, Cairo University, following patient referrals. Participants were recruited between October 2024 and April 2025 from the National Institute of Urology and Nephrology in Mataria, as well as the Department of Urology and Nephrology at Kasr Alaini Hospital. All diagnoses were verified by a consultant urologist. The study received ethical approval from the Institutional Review Board of the Faculty of Physical Therapy, Benha University, Egypt, and written informed consent was obtained from each participant prior to enrollment. Participants Individuals between 18 and 65 years of age presenting with OAB symptoms, confirmed through urodynamic testing, and diagnosed with ISCI classified as AIS C or D above the L1 spinal level, were considered eligible for inclusion in this study. Participants were required to be medically stable, able to follow study protocols, and willing to provide informed consent. Exclusion criteria included those with complete spinal cord injury (AIS A), current urinary tract infections, a history of pelvic malignancy, prior bladder or pelvic surgeries, or significant cognitive or psychiatric disorders. Simple randomization was applied to allocate participants into one of two groups: the EG, which received IFC, PFMT, motor MIT, and timed voiding (TV); and the CG, which received IFC, PFMT, and TV. The randomization process involved a computer-generated sequence created using dedicated software to ensure an equal number of participants in each group. Allocation concealment was maintained by placing group assignments in sealed, opaque envelopes, which were opened sequentially as participants were enrolled in the study. Outcome Measures 1. Urodynamic assessments 2. The International Consultation on Incontinence Questionnaire - Short Form (ICIQ-UI SF) 3. PFM strength Treatment procedures 1. IFC therapy 2. Timed voiding. 3. Motor imagery Training 4. PFMT

    Potential benefits

    Main benefits

    Bladder health/function

    Additional benefits

    General health

    Mental health and psychosocial factors

    Good to know: Potential benefits are defined as outcomes that are being measured during and/or after the trial.

    Wings for Life supports SCITrialsFinder

    Wings for Life has proudly initiated, led and funded the new version of the SCI Trials Finder website. Wings for Life aims to find a cure for spinal cord injuries. The not-for-profit foundation funds world-class scientific research and clinical trials around the globe.

    Learn more


    • Trial recruitment status
    • Ended
    • Trial start date
    • 1 Oct 2024
    • Organisation
    • Cairo University
    • Trial recruitment status
    • Ended
    • Trial start date
    • 1 Oct 2024
    • Organisation
    • Cairo University

    Wings for Life supports SCITrialsFinder

    Wings for Life has proudly initiated, led and funded the new version of the SCI Trials Finder website. Wings for Life aims to find a cure for spinal cord injuries. The not-for-profit foundation funds world-class scientific research and clinical trials around the globe.

    Learn more