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Construction and application of the continuious behavioral management model of knowledge-belief-behavior for spinal cord injury patients with neurogenic bladder

Construction and application of the continuious behavioral management model of knowledge-belief-behavior for spinal cord injury patients with neurogenic bladder

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049574
Enrollment
Unknown
Registered
2021-08-03
Start date
2019-06-01
Completion date
Unknown
Last updated
2022-04-19

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

Conditions

spinal cord injury

Interventions

control group:Water project
control group:intermittent catheterization
control group: conventional education model
the experimental group:knowledge-belief-behavior management
the experimental group:Water project
the experimental group:intermittent catheterization
the experimental group:medication

Sponsors

Tai’an City Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18-75 years, normal intelligence and language skills, able to cooperate in the evaluation questionnaire; 2. Meet the diagnostic criteria of MRI spinal cord injury, and the spinal cord is not completely detached. Meets International Continence Spcoety (ICS) diagnostic criteria for neurogenic bladder; 3. Patients with incomplete spinal cord injury above sacrum 2 and urinary dysfunction after acute spinal cord injury; 4. Admission to the hospital at the shock stage of spinal cord injury; 5. It has good tolerance to the urine volume measurement and urine routine inspection methods required for this study; 6. The patient's condition is stable and does not need rescue or monitoring treatment; 7. No organic urinary tract obstruction, urinary calculi, no metal implants near the bladder, and no pacemaker.

Exclusion criteria

Exclusion criteria: 1. Patients with long-term intravenous fluid infusion unable to control urine output per unit time; 2. Patients requiring long-term indwelling catheterization for disease reasons; 3. Patients or their family members unable to complete intermittent urinary catheterization; 4. Combined with serious complications, such as severe heart and kidney, Diabetes patients; 5. Patients who are unwilling to cooperate with the trial.

Design outcomes

Primary

MeasureTime frame
pelvic floor muscle surface electromyography evaluation;urodynamic evaluation;autonomous bladder establishment time;the knowledge, attitude, and behavioral volume questionnaire scores;

Countries

China

Contacts

Public ContactXiaoyu Wang

Rehabilitation Medicine Center of Tai'an City Central Hospital

15621327520@163.com+86 15621327520

Outcome results

None listed

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