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Evaluation of the Care Path of Patients Who Have Been Sexually Assaulted

Evaluation of the Care Path of Patients Who Have Been Sexually Assaulted, at Raymond Poincaré Hospital (France)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04078789
Acronym
AS UMJ/SMI RPC
Enrollment
250
Registered
2019-09-06
Start date
2022-06-30
Completion date
2024-09-30
Last updated
2022-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sexually Transmitted Diseases

Keywords

sex offenses, sexually transmitted diseases, traumatic injury

Brief summary

The main objective of this study is to describe the care pathway of patients presenting in the medico-judicial unit of the Raymond Poincaré Hospital in Garches, France, following a complaint for sexual assault and suggest ways to improvement of the care adapted to the characteristics of the participants.

Detailed description

AS secondary objectives, the study aims to: * Analyze the population of victims of sexual assault seen in consultation at the medico-judicial unit of Raymond Poincaré Hospital. * Analyze the decision elements of the initiation of the post-exposure treatment and evaluate them against the recommendations. * Analyze the data collected on the patients and their follow-up in consultation of infectious disease of the hospital of Garches following a sexual assault. * Identify obstacles encountered by participants to follow the complete follow-up path. For this purpose the data collection will be done initially within the forensic unit of Raymond Poincaré Hospital. Then, in a second step, the patients requiring the setting up of a post-exposure treatment, are addressed in the service of infectious diseases. The compilations of the data necessary for the study will then be continued until 3 months after the sexual assault. For the collection of data, they will be based on the medical records of the victims.

Interventions

None listed

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 120 Years
Healthy volunteers
No

Inclusion criteria

* People declared being victim of sexual assault; * Consult at medical-legal unit; * Judicial requirement.

Exclusion criteria

\- Absence of judicial requirement.

Design outcomes

Primary

MeasureTime frameDescription
post-exposure prophylaxis requirement and surveillance terminationat 1 yearPrevalence of a consultant victim at the medico-legal unit, requiring post-exposure prophylaxis and completing their post-sexual assault surveillance.

Secondary

MeasureTime frameDescription
Consulting at the medico-legal unitat 1 yearDescription of victims consulting at the medico-legal unit.
Follow-up in medico-legal unitat 1 yearFollow-up of the start of the post-exposure prophylaxis: indication, difficulty of the prescription, respect of the recommendations.
Follow-up in the infectious diseases departmentat 1 yearDescription of the patients followed in the department of acute medicine specializing in infectious diseases sent by the medico-legal unit following sexual assault: monitoring of sexually transmitted infections, aspects of psychological care, state of coverage vaccine, rate of completion, causes of cessation of the treatment, reasons for the failure of follow-up.

Contacts

Primary ContactCéline Dufort, MD
céline.durfort@aphp.fr+33147107698
Backup ContactDhiba Marigot-Outtandy, MD
dhiba.marigot-outtandy@aphp.fr+33147107770

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026