Heart Rate Variability and Anxiety During Urinary Bladder Catheterization
Study Details
Study Description
Brief Summary
This is a prospective, randomised study investigating the physical and psychological experience of intermittent catherization in adult individuals following spinal cord injury (SCI).
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
Given that intermittent catheterization is the recommended method of bladder management in individuals with SCI, it is crucial that the potentially negative cardiovascular and psychological responses to this procedure are examined. Individuals will undergo self-catherization, then two standard of care catherization procedures performed by an experienced urology nurse, while either blinded to or aware of time of catheterization. Continuous cardiovascular monitoring will be in place throughout all three procedures. Assessment of anxiety will be administered pre- and post- each procedure.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Individuals with motor-complete SCI Individuals with motor sensory complete injury (AIS A/B) |
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 catherization Catherization 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 catherization Catherization will be conducted following standard clinic procedure by experience urology nurse.
|
| Experimental: Individuals with motor-incomplete SCI Individuals with motor sensory incomplete injury (AIS C/D) |
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 catherization Catherization 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 catherization Catherization will be conducted following standard clinic procedure by experience urology nurse.
|
Outcome Measures
Primary Outcome Measures
- BP during self-catheterization [During self-catheterization]
Systolic and diastolic BP (mmHg) will be measured continuously (beat-by-beat) via finger photoplethysmography, corrected to brachial pressure. BP will be measured 5 minutes prior to and then throughout the self-catheterization procedure.
- HR during self-catheterization [During self-catheterization]
HR (BPM) will be recorded continuously via one-lead electrocardiogram. HR will be measured 5 minutes prior to and then throughout the self-catheterization procedure.
- BP during catheterization performed by urology nurse, participant blinded to time of procedure [During catheterization performed by urology nurse, participant blinded to time of procedure]
Systolic and diastolic BP (mmHg) will be measured 5 minutes prior to and then throughout the standard of care catheterization performed by an experienced urology nurse, while the participant is blinded to time of procedure.
- HR during catheterization performed by urology nurse, participant blinded to time of procedure [During catheterization performed by urology nurse, participant blinded to time of procedure]
HR (BPM) will be measured 5 minutes prior to and then throughout the standard of care catheterization performed by an experienced urology nurse, while the participant is blinded to time of procedure.
- BP during catheterization performed by urology nurse, participant aware of time of procedure [During catheterization performed by urology nurse, participant aware of time of procedure]
Systolic and diastolic BP (mmHg) will be measured 5 minutes prior to and then throughout the standard of care catheterization performed by an experienced urology nurse, while the participant is aware of time of procedure.
- HR during catheterization performed by urology nurse, participant aware of time of procedure [During catheterization performed by urology nurse, participant aware of time of procedure]
HR (BPM) will be measured 5 minutes prior to and then throughout the standard of care catheterization performed by an experienced urology nurse, while the participant is aware of time of procedure.
Secondary Outcome Measures
- Baseline trait anxiety [During screening]
The 7-item General Anxiety Disorder (GAD) scale will be used to measure participants' anxiety. The GAD-7 sum score will be calculated, ranging from 0 to 21, with higher score indicating more severe anxiety symptoms.
- Change in state anxiety in the context of self-catheterization (STAIS-5) [5 minutes before and 5 minutes after self-catheterization]
The State-Trait Anxiety Inventory - State, 5 item version (STAIS-5) will be used to measure participants' state anxiety prior to and after self-catheterization. Sum score of the STAIS-5 will be calculated, which ranges between 5 to 20, with higher score indicating greater state anxiety.
- Change in state anxiety in the context of self-catheterization (GA-VAS) [5 minutes before and 5 minutes after self-catheterization]
The Global Anxiety-Visual Analogue Scale (GA-VAS) will be used to measure participants' state anxiety prior to and after self-catheterization. Rating can range between 0 to 10, with higher rating on the GA-VAS indicates greater state anxiety.
- Change in state anxiety in the context of catheterization performed by urology nurse, participant blinded to time of procedure (STAIS-5) [5 minutes before and 5 minutes after catheterization performed by urology nurse, participant blinded to time of procedure]
The STAIS-5 will be used to measure participants' state anxiety prior to and after catheterization procedure performed by an experienced urology nurse, while the participant is blinded to time of procedure. Sum score of the STAIS-5 will be calculated, which ranges between 5 to 20, with higher score indicating greater state anxiety.
- Change in state anxiety in the context of catheterization performed by urology nurse, participant blinded to time of procedure (GA-VAS) [5 minutes before and 5 minutes after catheterization performed by urology nurse, participant blinded to time of procedure]
The GA-VAS will be used to measure participants' state anxiety prior to and after catheterization procedure performed by an experienced urology nurse, while the participant is blinded to time of procedure. Rating can range between 0 to 10, higher rating on the GA-VAS indicates greater state anxiety.
- Change in state anxiety in the context of catheterization performed by urology nurse, participant aware of time of procedure (STAIS-5) [5 minutes before and 5 minutes after catheterization performed by urology nurse, participant aware of time of procedure]
The STAIS-5 will be used to measure participants' state anxiety prior to and after catheterization procedure performed by an experienced urology nurse, while the participant is aware of time of procedure. Sum score of the STAIS-5 will be calculated, which ranges between 5 to 20, with higher score indicating greater state anxiety.
- Change in state anxiety in the context of catheterization performed by urology nurse, participant aware of time of procedure (GA-VAS) [5 minutes before and 5 minutes aftercatheterization performed by urology nurse, participant aware of time of procedure]
The GA-VAS will be used to measure participants' state anxiety prior to and after catheterization procedure performed by an experienced urology nurse, while the participant is aware of time of procedure. Higher rating on the GA-VAS indicates greater state anxiety.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Male or female, 18-70 years of age
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Any chronic traumatic SCI with either motor sensory complete injury (AIS A/B, N=10) or motor sensory incomplete injury (AIS B/D, N=10).
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At least 1 year post injury, and at least 6 months from any spinal surgery
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Hand function sufficient to perform intermittent catheterization for management of urinary bladder drainage
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Must provide informed consent and be able to understand and complete study-related questionnaires (must be able to understand and speak English or have access to an appropriate interpreter as judged by the investigator)
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Willing and able to comply with clinic visit and study-related procedures
Exclusion Criteria:
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Signs or known current urinary tract infection, or other inflammatory conditions of bladder/urethra
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Currently taking beta blockers or other medications that may affect heart rate
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History of ureteral injury
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History of any urinary diversion procedures, including but not limited to bladder augmentation, cystectomy, neo bladder, pouch reservoir, ileal conduit, Mitrofanoff appendicovesicostomy
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For women of childbearing potential, currently pregnant
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A member of the investigational team or his/her immediate family Presence of severe acute medical issue and use of any specific medication or treatment that, in the investigator's judgement, would adversely affect the participant's participation in the study
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Blusson Spinal Cord Centre | Vancouver | British Columbia | Canada | V5Z 1M9 |
Sponsors and Collaborators
- University of British Columbia
- ConvaTec Inc.
- Vancouver Coastal Health
- International Collaboration on Repair Discoveries
Investigators
- Principal Investigator: Andrei Krassioukov, MD,PhD,FRCPC, University of British Columbia
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- H22-00971