Analysis of Factors Associated With Delayed Medical Consultation for Testicular Torsion Among Adolescents in the Haut-Rhin Department Between 2020 and 2025 (TORSADO)

May 18, 2026 updated by: Centre Hospitalier de Colmar

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

Recruiting

Intervention / Treatment

Study Type

Observational

Enrollment (Estimated)

150

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Colmar, France, 68000
        • Recruiting
        • Centre Hospitalier de Colmar
        • Contact:
        • Principal Investigator:
          • Dorine Combescot
        • Sub-Investigator:
          • Sandy Jochault-Ritz

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Teenagers attending at Colmar Hospital

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Dorine Combescot, Hôpitaux Civils de Colmar
  • Principal Investigator: Sandy Jochault-Ritz, Hôpitaux Civils de Colmar

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 13, 2026

Primary Completion (Estimated)

September 30, 2026

Study Completion (Estimated)

December 31, 2026

Study Registration Dates

First Submitted

April 21, 2026

First Submitted That Met QC Criteria

April 21, 2026

First Posted (Actual)

April 28, 2026

Study Record Updates

Last Update Posted (Actual)

May 20, 2026

Last Update Submitted That Met QC Criteria

May 18, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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