West China Second University Hospital, Sichuan University
Chengdu, Sichuan, China
Location status: Recruiting
Recruiting
NCT Number: NCT06529107
Conversion of Evidence and Applied Research on Intermittent Catheterization After Radical Hysterectomy
In this study, the investigators summarize the existing best evidence of intermittent catheterization in patients after radical cervical cancer surgery from the perspective of clinical translation of evidence through systematic search, evaluation and evidence integration, construct a nursing protocol of intermittent catheterization for patients after radical cervical cancer surgery based on the best evidence combined with the clinical context, and explore the clinical application effect of the above nursing protocol. It will provide a reference basis for the development of the standardization and management of intermittent catheterization for postoperative patients with cervical cancer in China, as well as the development of guidelines for intermittent catheterization after radical cervical cancer surgery.
Recruiting
Interested in participating?
Request InfoKey information
Age range
18 year and older
Sex eligibility
Female
Study type
Interventional
Phase
Not applicable
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Age ≧ 18 years old
- Radical cervical cancer surgery and intermittent catheterization were performed at the Institute's hospital
- Patients or their family members can operate a smartphone
- No cognitive or psychiatric disorders, and can communicate effectively
Exclusion criteria
- People with serious heart, brain, lung and other important organ diseases
- People with water, electrolyte, acid-base balance disorders at the beginning of intermittent catheterization
- People with previous serious renal diseases, bladder and urethra surgery
- People with urinary tract infections
- People who did not complete all interventions or data collection
- People who voluntarily withdrew from the study or died during the study period;
- Refuse to participate in this study
Treatment and study plan
intermittent catheterization protocol based on the best evidence
BehavioralA best evidence-based protocol for intermittent catheterization after radical cervical cancer surgery
Primary outcomes
-
Incidence of urinary complications
Time frame: Within 2 months of discharge
the occurrence of urologic complications within 2 months after discharge of the patients from the hospital for follow-up, which in this study included urinary tract infections, urethral injuries, bladder stones, hydronephrosis
Secondary outcomes
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Intermittent Catheterization Compliance Scale
Time frame: Pre-intervention, immediately post-intervention, and 1 month post-discharge
A questionnaire was used to investigate patients' adherence to carrying out intermittent catheterization before the intervention, immediately after the intervention, and 1 month after discharge from the hospital. Higher scores indicate better adherence.
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12-Item Short Form Survey
Time frame: Pre-intervention, immediately post-intervention, and 1 month post-discharge
A questionnaire was used to investigate patients' quality of life before and immediately after the intervention and 1 month after discharge. Higher scores indicate better quality of life.
-
Self-Rating Anxiety Scale
Time frame: Pre-intervention, immediately post-intervention, and 1 month post-discharge
A questionnaire was used to investigate patients' anxiety before and immediately after the intervention and 1 month after discharge from the hospital. Higher scores indicate greater anxiety.
-
Intermittent Catheterization Confidence Scale
Time frame: Pre-intervention, immediately post-intervention, and 1 month post-discharge
A questionnaire was used to investigate patients' self-efficacy before and immediately after the intervention and 1 month after discharge from the hospital. Higher scores indicate greater confidence.
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Utilization of health services
Time frame: Within 2 months of discharge
Follow-up to record the number of unplanned readmissions, outpatient visits, and emergency room visits within 2 months of discharge and to evaluate the patient's health service utilization
Study contacts
Contact information is provided by the study sponsor or research team.
Sponsors and collaborators
Lead sponsor
West China Second University Hospital
Other
Registry information
Important dates
- Study start
- 2024
- Primary completion
- 2024
- Study completion
- 2024
- First posted
- Jul 31, 2024
- Registry last updated
- Jul 31, 2024
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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