Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
100 participants
OBSERVATIONAL
2020-01-01
2021-08-31
Brief Summary
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The study was conducted in a Neuro-urology Department of a University Hospital. To allow a full psychometric validation of the questionnaire, the study protocol included 3 steps: qualitative interviews, feasibility study and validation study. The inclusion criteria were to be aged \> 18 years and to have OAB symptoms according to the ICS definition and secondary to a neurogenic dysfunction.
First step of the study consisted in a review literature on Pubmed to explore the different side effects secondary to antimuscarinic treatment and do determine which tools were available. In addition, we conducted semi-structured interviews on 30 patients suffering from OAB.
For this feasibility study, 30 patients were included. They had to rate each item to evaluate comprehension, acceptation and pertinence with a three-points Likert scale from response "0: not at all or quite" to "2: perfectly".
Validation study: 100 patients Content validity was assessed by the panel of experts. Internal consistency reliability was calculated using the α coefficient of Cronbach. Each response has been transformed in a numeric value to perform this test. Alpha coefficient of Cronbach was considered as very good if \> 0.7.
Test-retest reliability was tested using the intraclass correlation coefficient (ICC) which was significant over 0.7.
Objective was to validate this questionnaire with good or very good psychometric properties. Primary outcome was Alpha coefficient of Cronbach and ICC ≥ 0,7.
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Detailed Description
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The study was conducted in a Neuro-urology Department of a University Hospital. To allow a full psychometric validation of the questionnaire, the study protocol included 3 steps: qualitative interviews, feasibility study and validation study. The inclusion criteria were to be aged \> 18 years and to have OAB symptoms according to the ICS definition and secondary to a neurogenic dysfunction.
First step of the study consisted in a review literature on Pubmed to explore the different side effects secondary to antimuscarinic treatment and do determine which tools were available. In addition, we conducted semi-structured interviews on 30 patients suffering from OAB.
Feasibility Study For this feasibility study, 30 patients were included. They had to rate each item to evaluate comprehension, acceptation and pertinence with a three-points Likert scale from response "0: not at all or quite" to "2: perfectly".
Validation study: 100 patients Content validity was assessed by the panel of experts. Internal consistency reliability was calculated using the α coefficient of Cronbach. Each response has been transformed in a numeric value to perform this test. Alpha coefficient of Cronbach was considered as very good if \> 0.7.
Test-retest reliability was tested using the intraclass correlation coefficient (ICC) which was significant over 0.7. The first questionnaire was filled at the end of the first consultation and patients had to answer a second questionnaire (filled at home) 7 days after the first consultation.
Objective was to validate this questionnaire with good or very good psychometric properties. Primary outcome was Alpha coefficient of Cronbach and ICC ≥ 0,7.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Questionnaire
validated questionnaire to assess side effects secondary to antimuscarinics treatment in neurogenic bladder
Eligibility Criteria
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Inclusion Criteria
* neurogenic bladder
* antimuscarinic treatment
Exclusion Criteria
18 Years
100 Years
ALL
No
Sponsors
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Pierre and Marie Curie University
OTHER
Responsible Party
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Gérard Amarenco
Clinical professor, Head of neuro urology department, APHP, tenon Hospital, Paris, France
Principal Investigators
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Gérard AMARENCO, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Sorbonne University, GRC 001, GREEN, APHP, Hopital Tenon, France
Locations
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department of Neuro-Urology, Hôpital Tenon
Paris, , France
Countries
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Other Identifiers
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GREEN GRC-01
Identifier Type: -
Identifier Source: org_study_id
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