- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05121623
Inappropriate Sexual Behaviour of Patients Towards French General Practitioners (#MedTooFr)
March 31, 2022 updated by: Centre Hospitalier Universitaire de la Réunion
Inappropriate Sexual Behaviour (ISB) of Patients Towards French General Practitioners: Prevalence, Nature and Impact on Professional Practice
Occupational sexual harassment (HS) has come to the fore in recent years, particularly with the #MeToo social movement that has encouraged women victims of sexual violence to speak out around the world.
The medical profession is not exempt from this phenomenon, whether during the training or professional life of practitioners.
In France, very little data is available on this subject, particularly among general practitioners.
However, the specific nature of the doctor-patient relationship in general practice makes it a potentially high-risk setting.
Furthermore, practitioners' experiences of inappropriate sexual behaviour (ISB) can lead to changes in professional practice, and can thus directly influence the quality of care provided to patients.
It is also described in the literature that sexual harassment in physicians is independently associated with a decrease in job satisfaction and sense of security at work, and may be associated with an altered mental health status.
To date, the only French studies on ISB and HS in medicine have focused on the period of medical study, and none have looked at the particular problem of the patient as perpetrator of the violence.
It is in this context that it has been decided to set up this cross-sectional study with the aim of evaluating the prevalence of ISB occurring during consultations with French general practitioners, to describe their characteristics and to evaluate the responses provided and the repercussions on professional practice.
Study Overview
Study Type
Observational
Enrollment (Actual)
570
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Saint-Pierre, Réunion
- CHU de la Réunion
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
General practitioners in private practice in France.
Description
Inclusion Criteria:
- Any general practitioner
- Male or female
- Sole or mixed private practice
- Installed or substitute
- Having completed their internship in general medicine
- With or without a thesis
- Practising alone, in a group practice or in a health centre -
Exclusion Criteria:
- Specialty other than general medicine
- Exclusive hospital or salaried activity
- Refusal to participate
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Prevalence and nature of inappropriate sexual behaviour of patients towards general practitioners in private practice in France
Time Frame: Once at the inclusion visit
|
Determined by auto-administered questionnaire (sociodemographic data, personal experience, author's characteristics, reactions and answers provided by the practitioners)
|
Once at the inclusion visit
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Prevalence and nature of Inappropriate sexual behavior between men and women
Time Frame: Once at the inclusion visit
|
To compare the prevalence and nature of Inappropriate sexual behavior according to the gender of the responding physicians determined by auto-administered questionnaire
|
Once at the inclusion visit
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Risk factors associated with sexual inapropriate behavior
Time Frame: Once at the inclusion visit
|
Identify the risk factors associated determined by auto-administered questionnaire (author's characteristics provided by the practitioners)
|
Once at the inclusion visit
|
Responses of general practitioners to such a situation
Time Frame: Once at the inclusion visit
|
Types of responses provided by general practitioners to such a situation determined by auto-administered questionnaire (answers provided by the practitioners)
|
Once at the inclusion visit
|
Impact and changes on professional practice and personal life.
Time Frame: Once at the inclusion visit
|
Describe the impact and changes on professional practice and personal life determined by auto-administered questionnaire (reactions provided by the practitioners)
|
Once at the inclusion visit
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
January 15, 2022
Primary Completion (Actual)
January 15, 2022
Study Completion (Actual)
March 22, 2022
Study Registration Dates
First Submitted
November 4, 2021
First Submitted That Met QC Criteria
November 4, 2021
First Posted (Actual)
November 16, 2021
Study Record Updates
Last Update Posted (Actual)
April 1, 2022
Last Update Submitted That Met QC Criteria
March 31, 2022
Last Verified
March 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- 2021/CHU/18
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.
Clinical Trials on Sex Behavior
-
The University of Hong KongCompletedAdolescent Behavior | Behavior, Sex | Sex, UnsafeHong Kong
-
Eunice Kennedy Shriver National Institute of Child...UnknownAdolescent Behavior | Sex BehaviorUnited States
-
Eunice Kennedy Shriver National Institute of Child...UnknownChild Behavior | Sex BehaviorUnited States
-
University PotiguarUniversidade Federal do Ceará; Federal Institute of Science and Technology...Completed
-
Chinese University of Hong KongRecruiting
-
Uludag UniversityCompleted
-
University Hospital, CaenCompletedSex Behavior | TeenagerFrance
-
Child TrendsFamily and Youth Services Bureau; Latin American Youth Center; Equimundo:Center...Recruiting
-
Sakarya UniversityCompletedSexual Education in Women Based On The Plissit Model On Awareness And Attitude in Midwifery StudentsCancer | Educational Problems | Sex BehaviorTurkey
-
Child TrendsPromundo, United States; Latin American Youth CenterCompletedSexual Behavior | Unprotected SexUnited States
Clinical Trials on Questionnaire
-
H. Lee Moffitt Cancer Center and Research InstituteSan Diego State University; University of Minnesota; University of ArizonaCompletedAnxiety | Psychological StressUnited States
-
Centre Hospitalier Universitaire de NiceCompletedGeneral Population | TDAH | Children Aged 5 to 18 YearsFrance
-
Minneapolis Veterans Affairs Medical CenterUnited States Department of DefenseCompletedLower Limb Amputation Below Knee (Injury) | Lower Limb Amputation Above Knee (Injury)United States
-
NSABP Foundation IncNational Cancer Institute (NCI)Completed
-
Imperial College LondonRoyal Marsden NHS Foundation Trust; University College London Hospitals; The... and other collaboratorsCompleted
-
Stanford UniversityRecruitingAstigmatism | Nearsightedness | FarsightednessUnited States
-
University of LiegeCompletedCritical Illness | Covid19 | Psychological Stress | FamilyBelgium
-
Rabin Medical CenterCompleted
-
Imperial College Healthcare NHS TrustNot yet recruitingCervical Myelopathy
-
National Taiwan University HospitalNational Taiwan UniversityUnknownComputerized Physician Order EntryTaiwan