Conversion of Evidence and Applied Research on Intermittent Catheterization After Radical Hysterectomy
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorWest China Second University Hospital
About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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
Disqualifiers
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
Trial design
Design model
Parallel
Treatments tested in this trial
intermittent catheterization protocol based on the best evidence
BehavioralA best evidence-based protocol for intermittent catheterization after radical cervical cancer surgery
Treatment groups
70 Participants
are divided into 2 treatment groupsGroup A: A best evidence-based protocol for intermittent catheterizationExperimental treatment 1 intervention
Group B: Routine intermittent catheterization careNo intervention 0 interventions
Trial outcomes
Primary outcomes
1
Incidence of urinary complications
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
Time frame
Within 2 months of dischargeSecondary outcomes
1
Intermittent Catheterization Compliance Scale
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.
Time frame
Pre-intervention, immediately post-intervention, and 1 month post-discharge2
12-Item Short Form Survey
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.
Time frame
Pre-intervention, immediately post-intervention, and 1 month post-discharge3
Self-Rating Anxiety Scale
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.
Time frame
Pre-intervention, immediately post-intervention, and 1 month post-discharge4
Intermittent Catheterization Confidence Scale
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.
Time frame
Pre-intervention, immediately post-intervention, and 1 month post-dischargeSponsors and contacts
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Source ClinicalTrials.gov