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Recruiting NCT07519928

NCT07519928 Exploring the Feasibility and Benefits of Implementing Pelvic Floor Muscle Training During Inpatient Rehabilitation for People With Spinal Cord Injury

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Clinical Trial Summary
NCT ID NCT07519928
Status Recruiting
Phase —
Sponsor University of British Columbia
Condition Spinal Cord Injuries (SCI)
Study Type INTERVENTIONAL
Enrollment 50 participants
Start Date 2026-04-01
Primary Completion 2027-09-30

Eligibility & Interventions

Sex All sexes
Min Age 19 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Pelvic Floor Muscle Physiotherapy

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 50 participants in total. It began in 2026-04-01 with a primary completion date of 2027-09-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this clinical study is to determine the feasibility and explore the potential benefits of pelvic floor muscle training during inpatient SCI rehabilitation on urinary, bowel, and sexual function and quality of life in people with SCI. The main questions it aims to answer are: 1. What is the feasibility of recruiting inpatients from SCI rehabilitation to a pelvic floor muscle training program? 2. What is the feasibility and acceptance of the implementation of a pelvic floor muscle training program in SCI inpatient rehabilitation? 3. What are the potential effects of a pelvic floor muscle training program implemented in SCI inpatient rehabilitation on bladder, bowel, and sexual function and quality of life? Participants will be asked to complete a series of assessments (questionnaires, physical assessments) before and after a 6-week intervention of pelvic floor physical therapy.

Eligibility Criteria

Inclusion Criteria: 1. Are at least 19 years of age. 2. Have a traumatic or non-traumatic SCI 3. Are able to perform a voluntary anal contraction 4. Present with bladder or urinary tract dysfunction from SCI 5. Are a current inpatient at GF Strong Rehabilitation Center and are expected to remain as an inpatient for at least 6 weeks after the time of consent. 6. Are able to speak and understand English. Exclusion Criteria: 1. Present with symptoms of lower motor neuron injury to the sacral segments (e.g. negative anal and bulbocavernosus reflexes) 2. Present with any other condition besides SCI that impacts the pelvic floor muscles or other pelvic structures 3. Are planning to receive intra-detrusor Botox injections in the next 3 months 4. Have a brain injury or other condition that interferes with their ability to follow instructions 5. Are using a ventilator 6. Have severe and unmanaged spasticity (involuntary muscle tightness or spasms) or contractures (prolonged muscle/joint stiffness) 7. Are unable to tolerate transfers to or lie on a physical therapy table 8. Experience severe pain that interferes with their ability to participate in pelvic floor muscle training

Contact & Investigator

Central Contact

Jiho Song

✉ lamlab@icord.org

📞 604-675-8815

Frequently Asked Questions

Who can join the NCT07519928 clinical trial?

This trial is open to participants of all sexes, aged 19 Years or older, studying Spinal Cord Injuries (SCI). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07519928 currently recruiting?

Yes, NCT07519928 is actively recruiting participants. Contact the research team at lamlab@icord.org for enrollment information.

Where is the NCT07519928 trial being conducted?

This trial is being conducted at Vancouver, Canada.

Who is sponsoring the NCT07519928 clinical trial?

NCT07519928 is sponsored by University of British Columbia. The trial plans to enroll 50 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology