Effects Of App-Supported Transitional Care On Neurogenic Bladder In Spinal Cord Injury Patients
2026年6月10日 更新者：Tian Zhang、Xiamen University
Effects Of App-Supported Transitional Care On Bladder Function And Quality Of Life in Patients With Neurogenic Bladder After Incomplete Spinal Cord Injury: A Randomised Controlled Trial
This is a single-blind randomized controlled trial for patients with neurogenic bladder after incomplete spinal cord injury.
Participants are randomly divided into two groups.
The control group receives routine transitional nursing and telephone follow-up, while the intervention group gets 4-week app-supported transitional care including health education, bladder recording and online consultation.
After intervention, bladder residual urine, urinary tract infection rate, self-care ability and quality of life are compared between two groups.
研究概览
地位
完全的
详细说明
Neurogenic bladder is a common complication after incomplete spinal cord injury, which easily leads to recurrent urinary tract infection and decreased quality of daily life.
Traditional transitional follow-up is limited by time and space.
This study adopts single-blind parallel-group RCT design.
Eligible patients are randomly allocated at a 1:1 ratio.
Control group receives standard inpatient nursing plus conventional post-discharge follow-up; intervention group receives identical inpatient care plus systematic app-based transitional care for 4 weeks.
Primary outcomes are post-void residual urine volume and urinary tract infection incidence.
Secondary outcomes contain self-care ability and quality of life assessed by standardized scales.
All indicators are tested at baseline and 4 weeks after intervention to verify the clinical effect of app-assisted transitional nursing.
研究类型
介入性
注册 (实际的)
88
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。
学习地点
-
-
Jilin
-
Siping、Jilin、中国、136000
- Siping Central People's Hospital
-
-
参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
Diagnosed with neurogenic bladder secondary to incomplete spinal cord injury; Age ranging from 18 to 75 years old; Clear consciousness, capable of cooperating with nursing assessment and mobile APP follow-up management; Voluntarily sign written informed consent. -
Exclusion Criteria:
Combined with severe renal insufficiency, malignant tumor or other life-threatening severe systemic diseases; History of previous bladder reconstructive surgery; Cognitive impairment unable to independently operate mobile APP; Refuse to continue follow-up or withdraw voluntarily during the research period.
-
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
- 主要用途：治疗
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
有源比较器：Control Group
Patients receive routine standardized inpatient bladder nursing, only one-time routine telephone follow-up after discharge without APP-based transitional care intervention
|
routine standardized inpatient bladder nursing
|
|
实验性的：Intervention Group
Same routine inpatient nursing as control group plus 4 weeks of systematic APP-supported transitional care including health education, voiding record management and online nurse consultation.
|
routine standardized inpatient bladder nursing
Four-week continuous transitional nursing service via mobile APP for patients with neurogenic bladder after incomplete spinal cord injury, including disease-related health education, real-time voiding record, regular nursing reminder and online one-on-one nurse consultation, which differs from routine single telephone follow-up in control group.
|
研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Incidence of urinary tract infection
大体时间：Within 4 weeks after subject enrollment
|
Count the occurrence of urinary tract infection within 4-week follow-up and calculate infection incidence of each group.
|
Within 4 weeks after subject enrollment
|
|
Post-void residual urine volume
大体时间：Baseline and 4 weeks after intervention
|
Bladder residual urine volume is measured by ultrasonic examination at baseline and after 4 weeks of nursing intervention to compare the difference between two groups.
|
Baseline and 4 weeks after intervention
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Self-care ability and quality of life score
大体时间：Baseline and 4 weeks after intervention
|
Standardized scale scoring for self-care and quality of life before and after 4-week transitional nursing.
|
Baseline and 4 weeks after intervention
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2026年1月10日
初级完成 (实际的)
2026年5月1日
研究完成 (实际的)
2026年5月1日
研究注册日期
首次提交
2026年6月6日
首先提交符合 QC 标准的
2026年6月10日
首次发布 (实际的)
2026年6月11日
研究记录更新
最后更新发布 (实际的)
2026年6月11日
上次提交的符合 QC 标准的更新
2026年6月10日
最后验证
2026年6月1日
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- SKYLW-2024-001
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)？
不
IPD 计划说明
Individual participant raw data will not be shared publicly due to patient privacy protection and relevant hospital data management regulations.
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.