Heart Rate Variability and Anxiety During Urinary Bladder Catheterization

NCT05380661 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 22

Last updated 2026-04-28

No results posted yet for this study

Summary

This is a prospective, randomised study investigating the physical and psychological experience of intermittent catheterization in adult individuals following spinal cord injury (SCI).

Conditions

  • Spinal Cord Injuries
  • Urinary Bladder, Neurogenic
  • Anxiety State
  • Catheter Complications
  • Autonomic Dysreflexia

Interventions

PROCEDURE

Self-catheterization

Participants will perform self-catheterization, following the same routine for intermittent catheterization at home

PROCEDURE

Catheterization performed by urology nurse, participant blinded to time of procedure

Participant will undergo procedure to completely empty bladder; Participant in supine position, and resting blood pressure and heart rate will be recorded for period of 5 minutes prior to catheterization; Perineum and genital areas will be draped and they will be not aware about exact timing of catheterization Catheterization will be conducted following standard clinic procedure by experience urology nurse.

PROCEDURE

Catheterization performed by urology nurse, participant aware of time of procedure

Participant will undergo procedure to completely empty bladder; Participant in supine position, and resting BP and HR will be recorded for period of 5 minutes prior to catheterization; Perineum and genital areas will be visible to participant and they will be fully aware about exact timing of catheterization Catheterization will be conducted following standard clinic procedure by experience urology nurse.

Sponsors & Collaborators

  • ConvaTec Inc.

    collaborator INDUSTRY
  • Vancouver Coastal Health

    collaborator OTHER_GOV
  • International Collaboration on Repair Discoveries

    collaborator OTHER
  • University of British Columbia

    lead OTHER

Principal Investigators

  • Andrei Krassioukov, MD,PhD,FRCPC · University of British Columbia

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-07-15
Primary Completion
2026-04-16
Completion
2026-04-16

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05380661 on ClinicalTrials.gov