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Not yet recruitingNCT07106502PaTenSimUpdated Aug 6, 2025

Learning to Palpate the Child's Testicles Using Simulation

An interventional study of testicular palpation training on a mannequin in Testicular Positioning Anomalies and Cryptorchidism, sponsored by University Hospital, Angers. Not yet recruiting. Per ClinicalTrials.gov, last updated 2025-08-06.

Sponsored by University Hospital, Angers · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
62
Allocation
Randomized
Sex
All
01

Study summary

Hypothesis is that better training of medical students in the examination of boy's external genitalia could improve the diagnosis of testicular position anomalies. To this end, investigators already have created a model to train testicle palpation and recognition of testicular position anomalies. So investigator set up a monocentric randomized controlled trial in wich the medical students will be randomized into 2 groups : a control group receiging only book-based theoretical instruction on the examination of the external genitalia and testicular position anomalies, and a mannequin group receibing, in addition to this conventionnal instruction, simulation training on the mannequin Medical students will then attend a consultation with a child whose reason for coming to the hospital is a testicular positioning anomaly. Students clinical examination will be scored by the consulting senior, and the final diagnosis retained by the student will be compared with that retained by the consulting senior. The aim is to show that medical students who have trained on this new model are better, in terms of clinical examination and diagnostic, than students in the control group.

02

Conditions studied

  • Testicular Positioning Anomalies
  • Cryptorchidism

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Keywords

  • cryptorchidism
  • testicular palpation
03

In context

Cryptorchidism

40 studies on the registry are indexed under Cryptorchidism; 14 are open to participants now.

This study's planned enrollment of 62 is below the median of 70 across 26 interventional studies indexed under Cryptorchidism.

Browse Cryptorchidism studies →

Lead sponsor

University Hospital, Angers is the lead sponsor of 478 studies on the registry; 120 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Medical student who volunteers to take part in the study during their pediatric or pediatric surgery clerkship or at the simulation center

Exclusion criteria

Exclusion Criteria:

  • student non in pediatric intership or non in pediatric surgery intership or non at the simulation center intership
  • Student with previous simulation training in the examination of the external genitalia of children
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
62 participants (estimated)

Study arms

  • No intervention
    Control group
  • Experimental
    mannequin simulation-based learning group

    Procedure: testicular palpation training on a mannequin

Interventions

  • Proceduretesticular palpation training on a mannequin

    Study of testicular palpation training on a mannequin on the ability to perform a testicular examination and diagnose testicular positioning abnormalities

06

What researchers measure

Primary outcomes

  1. Rate of correct diagnoses

    The primary outcome will be the rate of correct diagnoses made by the medical students compared with the diagnosis made by the consultant surgeon.

    Time frame: Baseline

Secondary outcomes

  1. clinical examination score from 0 to 20

    to assess the student's clinical skills and the quality of the physical examination

    Time frame: Baseline

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 6, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07106502
Responsible party
Sponsor
First posted
Aug 6, 2025
Start date
Oct 1, 2025 (estimated)
Primary completion
Oct 1, 2026 (estimated)
Completion
Oct 1, 2026 (estimated)
Last update
Aug 6, 2025

Study contacts

Louise RENOULT
Contact
louise.renoult@chu-angers.fr
2 41 35 42 90 ext. +33
Louise RENOULT
study chair · University Hospital of Angers

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

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