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World Journal of Urology

, Volume 36, Issue 6, pp 883–887 | Cite as

Prospective randomised controlled trial of written supplement to verbal communication of results to patients at the time of flexible cystoscopy

  • Frank D’Arcy
  • Chew Lin Yip
  • Kiran Manya
  • Paul McGivern
  • Rustom P. Manecksha
  • Damien Bolton
  • Shomik Sengupta
Original Article

Abstract

Purpose

This trial assessed if written information on procedural findings and subsequent treatment improved understanding and reduced anxiety among patients undergoing day case flexible cystoscopy (FC).

Methods

Participants completed pre- and post-procedure questionnaires self-rating anxiety and feeling well informed on 5-point Likert scales. Supplemental written information was provided after FC to half the patients on a standardized template, according to randomized allocation. Comparisons between the groups were undertaken using the Wilcoxon test.

Results

Two hundred patients were recruited, with 171 evaluable questionnaires (83 from written group). The distribution of age, sex and prior FC, as well as the pre-procedure self-assessment of anxiety and understanding, was similar between the two groups. Patients receiving written information reported feeling better informed, with median (range) Likert score of 5 (4–5) compared to 4 (1–5) out of 5 (p < 0.0001) and less anxious (score 1 [1–4] compared to 2 [1–5] out of 5, p < 0.005), although all except four patients had an accurate understanding of the information provided (p = NS).

Conclusions

Written information at the time of FC leads to patients feeling better informed and less anxious, although verbal information alone appears to lead to an adequate understanding.

Clinical trial registration number

ACTRN12616000288426

Keywords

Flexible cystoscopy Information RCT Verbal Written 

Notes

Author contributions

FD’A: study procedures and implementation, and manuscript preparation. CLY and KM: protocol development and data collection. PM and RM: study procedures and implementation. DB: protocol development and infrastructure support. SS: protocol development, data collection and analysis, and manuscript preparation.

Compliance with ethical standards

Conflict of interest

The authors declare that they do not have any conflicts of interest to report.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.

Informed consent

Informed consent was obtained from all individual participants included in the study.

Supplementary material

345_2018_2233_MOESM1_ESM.pdf (13 kb)
Supplementary material 1 (PDF 12 kb)
345_2018_2233_MOESM2_ESM.pdf (33 kb)
Supplementary material 2 (PDF 33 kb)
345_2018_2233_MOESM3_ESM.pdf (16 kb)
Supplementary material 3 (PDF 15 kb)
345_2018_2233_MOESM4_ESM.docx (12 kb)
Supplementary material 4 (DOCX 13 kb)

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Urology DepartmentAustin HealthHeidelbergAustralia
  2. 2.Austin Department of SurgeryUniversity of MelbourneHeidelbergAustralia
  3. 3.Urology DepartmentGalway HospitalGalwayIreland
  4. 4.Urology DepartmentSt James HospitalDublinIreland
  5. 5.Eastern Health Clinical SchoolMonash UniversityBox HillAustralia

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