Development of a New Canadian Endourology Group Stent Symptom Score
Urologic DiseasesPlacement of a ureteral stent is a common urological intervention. For decades there was no valid measures available to assess quality of life issues in patients with ureteral stents, which has hampered the understanding of such symptoms and their true impact. In order to improve the outcomes associated with the placement of a stent, a validated tool is needed to measure its impact and the amount of undesirable effects it produces on patients requiring the placement of a stent. In 2003, the team of the Bristol Urological Institute developed a validated questionnaire called the: URETERAL STENT SYMPTOM QUESTIONNAIRE (USSQ). The questionnaire contains 38 items included in 6 sections. Despite the obvious need of a validated questionnaire, the latter remains unused by the community of peer urologists. Many of urologists consider it too long to be used in clinical practice and even for research purposes. This issue motivated the Canadian Endourology Group (CEG) to work collaboratively on the development of the CANADIAN ENDOUROLOGY GROUP STENT SYMPTOM SCORE (CEGSSS) in order to provide clinicians with a more useful and validated tool. To fulfill this objective, the CEG proceeds in three phases. Phase 1. A systematic, deliberative, and participatory approach mostly through face to face meetings, including patients, clinicians, and researchers in the field of Endourology to identify a minimum needs-based set of domains and items that are, clinically relevant to be included in the CEGSSS in order to ensure optimal uptake in the clinical setting. Phase 2. A pilot study to assess feasibility/acceptability and further refine the proposed set of items selected in phase 1 of the study. Phase 3. A multicentric prospective study to evaluate the validity, reliability and sensitivity to change of the CEGSSS.
This research project is conducted by the Canadian Endourology Group (CEG), a panel of experts in the field of endourology in Canada. The CEG is a national member-based organization dedicated to enabling the profession to provide the highest possible standards of endourological care and to advance the science of endourology by collaboratively:
1. Fostering excellence in endourological practice through advocacy, education, research and practice support tools,
2. Leading evidence-based clinical practice through the development of practice standards and guidelines in endourology,
3. Providing continuous professional development for Canadian endourologists along the career-path continuum,
4. Providing leadership in public education for endourological conditions.
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Conditions de participation
-
Sexe:
ALL -
Âges admissibles:
18 and up
Critères de participation
Inclusion Criteria:
* Age ≥ 18 years
* Patient with ureteral stent
* Ability to communicate in English
Exclusion Criteria:
* Inability to provide an informed consent due to physical or mental inability
* Active malignancy
* Obstruction
* Long-term stent (\>2 weeks)
Lieu de l'étude
St. Michael's Hospital - University of Toronto
St. Michael's Hospital - University of TorontoToronto, Ontario
Canada
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Dalhousie University
Dalhousie UniversityHalifax, Nova Scottia
Canada
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Royal Victoria Hospital- McGill University Health Centre
Royal Victoria Hospital- McGill University Health CentreMontréal, Quebec
Canada
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Alberta University - Northern Alberta Urology Centre
Alberta University - Northern Alberta Urology CentreEdmonton, Alberta
Canada
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Toronto General Hospital - University Health Network (UHN)
Toronto General Hospital - University Health Network (UHN)Toronto, Ontario
Canada
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Vancouver General Hospital
Vancouver General HospitalVancouver, British Columbia
Canada
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Centre Hospitalier de l'Université de Montréal (CHUM)
Centre Hospitalier de l'Université de Montréal (CHUM)Montréal, Quebec
Canada
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- Étude parrainée par
- Centre hospitalier de l'Université de Montréal (CHUM)
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT04909541