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Application of list-based video education in the health education of patients with daytime ureteroscopy lithotripsy

Application of list-based video education in the health education of patients with daytime ureteroscopy lithotripsy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094640
Enrollment
Unknown
Registered
2024-12-25
Start date
2024-12-25
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Ureteral Calculi

Interventions

control group:Conventional nursing, Oral education
intervetion group:video mission based on health education checklist

Sponsors

The affiliated hospital of southwest medical university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Age >=18 years and <=65 years; 2.Patients undergoing ureteroscopic lithotripsy for the first time with indwelling double J tubes; 3.Patients who are available for follow-up or telephone contact after discharge; 4.Patients with access to smartphones; 5.Those who have reading, comprehension and verbal communication skills and can complete the questionnaire independently or with the assistance of a researcher; 6.Patients gave informed consent and voluntarily participated in this study.

Exclusion criteria

Exclusion criteria: 1.People with severe mental illness or cognitive dysfunction, such as depression, dementia, etc; 2.Patients with severe heart, brain, kidney disease or other malignant diseases, such as heart failure, emphysema, kidney transplantation, etc; 3.People with abnormal coagulation function; 4.Patients with a history of ureteral surgery or ureteral stenosis; 5.Patients with prostate hyperplasia, cystitis, bladder tuberculosis and other diseases related to lower urinary tract symptoms; 6.Preoperative infection, intraoperative or postoperative ureteral perforation, rupture, mucosal avulsion, severe bleeding (Hb<=90g/L), sepsis and other complications occurred; 7.Patients with incomplete clinical data; 8.Pregnant or lactating women; 9.Clinical trial participants who are participating in other studies.

Design outcomes

Primary

MeasureTime frame
Discharge readiness;

Secondary

MeasureTime frame
Postoperative complication rate;Rate of unplanned readmission within one month after surgery;Postoperative quality of life;

Countries

China

Contacts

Public ContactXuying

The affiliated hospital of southwest medical university

960031734@qq.com+86 15283091563

Outcome results

None listed

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