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Effects of exoskeleton-assisted gait training on bowel and bladder function in individuals with incomplete spinal cord injury

Effects of exoskeleton-assisted gait training on bowel and bladder function in individuals with incomplete spinal cord injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117301
Enrollment
Unknown
Registered
2026-01-22
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal cord injury

Interventions

Exoskeleton-Assisted Walking Training Group :In addition to conventional physical therapy, participants in the intervention group will undergo exoskeleton-assisted walking training for 30 minutes per
Control Group :Conventional physical therapy

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Age between 20 and 70 years, with no restriction on sex; (2) Height between 1.42 m and 1.93 m; (3) Body weight less than 90 kg; (4) Injury type classified as ASIA grades B, C, or D, with the level of injury located in the cervical, thoracic, or lumbar regions; (5) NBSD score >= 13; (6) NBSS score >= 13.

Exclusion criteria

Exclusion criteria: (1) A Modified Ashworth Scale (MAS) score greater than 2 in bilateral lower-limb muscle spasticity; (2) Receipt of exoskeleton-assisted gait training within the past 6 months; (3) Hypertension, defined as systolic blood pressure >140 mmHg or diastolic blood pressure >90 mmHg despite pharmacological treatment; (4) Recent severe musculoskeletal disorders (e.g., unstable fractures of the limbs, severe osteoporosis); (5) Comorbidities or complications limiting cognitive or mobility function (e.g., psychiatric disorders, deep vein thrombosis of both lower limbs); (6) Body weight >100 kg; (7) Any other conditions deemed unsuitable for inclusion by the investigators.

Design outcomes

Primary

MeasureTime frame
Neurogenic Bowel Dysfunction Score, NBDS;Neurogenic Bladder Symptoms Score, NBSS;Adverse events;

Secondary

MeasureTime frame
Pelvic floor electromyographic assessment ;Bristol Stool Form Scale , BSS ; International Consultation on Incontinence Questionnaire–Urinary Incontinence Short Form, ICI-Q-Short Form;Spatiotemporal gait parameters;

Countries

China

Contacts

Public ContactHongchen He

West China Hospital, Sichuan University

hxkfhhc@126.com+86 189 8060 2262

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026