- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07554313
Analysis of Factors Associated With Delayed Medical Consultation for Testicular Torsion Among Adolescents in the Haut-Rhin Department Between 2020 and 2025 (TORSADO)
Analyse Des Facteurs de Retard à la Consultation Dans Les Torsions Testiculaires Chez Les Adolescents du Haut-Rhin Entre 2020 et 2025
The objective of this observational study is to identify the factors that influence whether or not an adolescent seeks immediate medical attention upon the onset of symptoms of testicular torsion. The main question it aims to answer is as follows:
What factors are associated with a delay in seeking medical care-defined as a time interval of 6 hours or more between the onset of symptoms and the first visit to Colmar Hospital-among adolescents aged 10 to 18 who underwent surgery for testicular torsion?
Participation in this study involves completing a questionnaire: the "Questionnaire for Assessing Factors Associated with Delay in Seeking Medical Care for Testicular Torsion in Adolescents."
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Nicolas Sachnine
- Phone Number: +33389126080
- Email: nicolassachnine@gmail.com
Study Contact Backup
- Name: Magali Eyriey
- Phone Number: +33389124810
- Email: cellule-promotion@ch-colmar.fr
Study Locations
-
-
-
Colmar, France, 68000
- Recruiting
- Centre Hospitalier de Colmar
-
Contact:
- Nicolas Sachnine
- Phone Number: +33389126080
- Email: nicolassachnine@gmail.com
-
Principal Investigator:
- Dorine Combescot
-
Sub-Investigator:
- Sandy Jochault-Ritz
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients who underwent surgery for suspected testicular torsion between 2020 and 2025 in the Paediatric Surgery Department of the Hôpitaux Civils de Colmar, following admission via the Paediatric A&E Department of the same hospital;
- Patients aged between 10 and 17 years at the time of admission;
- Participants who, after being informed, do not object to the use of their data for the purposes of this research;
- Holders of parental authority who, after being informed, do not object to the use of their children's data for the purposes of this research.
Exclusion Criteria:
- Any intraoperative diagnosis other than testicular torsion (e.g. hydatid torsion);
- Patients who cannot read and/or understand French;
- Participants or legal guardians who have expressed their refusal to take part in the study;
- Unusable patient records: insufficient data.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Early consultation
Patients who attended within strictly less than 6 hours of the onset of symptoms
|
Questionnaire for Assessing Factors Associated with Delay in Seeking Medical Care for Testicular Torsion in Adolescents
|
|
Delayed consultation
Patients who attended within six hours or more than the onset of symptoms.
|
Questionnaire for Assessing Factors Associated with Delay in Seeking Medical Care for Testicular Torsion in Adolescents
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The presence of at least one reported barrier to accessing healthcare
Time Frame: Before the first attending for testicular torsion
|
The primary outcome measure is the presence of at least one reported barrier to seeking healthcare, encompassing the reasons for delay cited by patients (embarrassment or shame about discussing symptoms, fear of hospitals, fear of being a bother, downplaying symptoms, or other reasons).
|
Before the first attending for testicular torsion
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The association between patients' prior knowledge of testicular torsion and the time taken to seek medical advice
Time Frame: Before the first attending for testicular torsion
|
The patient's prior awareness of the need to seek urgent medical attention in the event of acute testicular pain, assessed by a binary response (yes/no) to the questionnaire.
|
Before the first attending for testicular torsion
|
|
The role of those close to the individual, particularly parents or legal guardians, in the decision to seek medical advice.
Time Frame: Before the first attending for testicular torsion
|
Immediate notification by an adult (parent or legal guardian) as soon as symptoms appear, measured as a binary variable (yes/no).
|
Before the first attending for testicular torsion
|
|
The influence of the initial perception of symptom severity on the time taken to seek medical advice.
Time Frame: Before the first attending for testicular torsion
|
The initial subjective perception of symptom severity, assessed using an ordinal scale in response to the question 'When these symptoms/signs first appeared, how did you perceive them?' and analysed categorically. The scale is ranges from 0 = 'Not serious', 1 = 'Slightly serious, 2 = 'Moderately serious' to 3 = 'Extremly serious'. A higher score reflects higher perception of severity. |
Before the first attending for testicular torsion
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Dorine Combescot, Hôpitaux Civils de Colmar
- Principal Investigator: Sandy Jochault-Ritz, Hôpitaux Civils de Colmar
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Urogenital Diseases
- Genital Diseases
- Genital Diseases, Male
- Male Urogenital Diseases
- Spermatic Cord Torsion
- Health Care Quality, Access, and Evaluation
- Investigative Techniques
- Epidemiologic Methods
- Data Collection
- Health Care Evaluation Mechanisms
- Quality of Health Care
- Public Health
- Environment and Public Health
- Surveys and Questionnaires
Other Study ID Numbers
- HCC-019
- ID-RCB 2026-A00381-50 (Other Identifier: Agence nationale de sécurité du médicament et des produits de santé)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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