Adult DaughtersGyn-MGNCT05578924
Factors Associated With Gynecological Consultation by General Practitioner
An observational study of Adult Daughters, run by Université de Reims Champagne-Ardenne at 1 site in France.
Trial summary
Because of the shortage of doctors in France, notably gynaecologist, general practitioners are definitely an essential partner women's health. However, few of them regularly practice gynecological acts. Read more about this study
- Who is it for?
- Ages 18 years and older, women onlyHealthy volunteers can take part
- Conditions the study is for
- Adult Daughters
- What is being tested?
- " women group "
- How many people
- 2,000 participants
- Where
- 1 siteFrance
- Study dates
- 9 Sep 2022to 1 Feb 2023
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- Women only
- Healthy volunteers accepted
- Adult, Older adult
Study population: women aged more than 18 years old, who consent to participle to the study
Who may be able to join
- women aged more than 18 years old
- woman agreeing to participate to the study
Who cannot join
- women aged less than 18 years old
- woman not agreeing to participate to the study
Trial locations and contacts
1 site in 1 country.
France1 site, 1 recruiting
- Recruiting
Ufr Medecine Urca
Reims, 51100
Coralie Barbe, 326913665 ext. +33
About this study
Because of the shortage of doctors in France, notably gynaecologist, general practitioners are definitely an essential partner women's health. However, few of them regularly practice gynecological acts.
A lot of studies have studied why general doctors not practice gynecological acts but it would necessary to include the women's perspective.
Read the detailed description
The aim of the study will be identify women's factors associated with gynaecological consultation by the general practitioner.
- Conditions
- Adult Daughters
- Being tested
- " women group "
- Keywords
- Adult women, gynecological acts, general practitioners
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
" women group "Other
women aged more than 18 years old
What is being measured
The primary outcome is the main question the study is designed to answer.
Acceptance of gynecological consultation with a general practitioner
would the woman agree to consult a general practitioner for a gynecological reason ? (Yes or No)
Measured: Day 0
Secondary outcomes (1)
Women's knowledge of general practitioner gynecology competences
Does woman know that a general practitioner is able to perform gynecological acts? (Yes or No)
Measured: Day 0
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Oct 2022
- Study start9 Sep 2022
- Primary completion1 Dec 2022 (estimated)
- Study completion1 Feb 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Adult DaughtersStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case only
- Time perspective
- Cross-sectional
- Enrolment
- 2,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Université de Reims Champagne-Ardenne
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- barbe coralie, Principal investigator, pratictioner
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05578924
- Sponsor's protocol ID
- 2022_RIPH_008_Gyn-MG
- Acronym
- Gyn-MG
- Status last verified
- Oct 2022
- First submitted
- 10 Oct 2022
- Last updated
- 18 Oct 2022
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 18 Oct 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Factors Associated With Gynecological Consultation by General Practitioner
- ClinicalTrials.gov ID
- NCT05578924
- Acronym / sponsor ID
- Gyn-MG / 2022_RIPH_008_Gyn-MG
- Conditions
- Adult Daughters
- Keywords
- Adult women, gynecological acts, general practitioners
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 2,000 participants (estimated)
- Lead sponsor
- Université de Reims Champagne-ArdenneUniversity, hospital or other
- Study start
- 9 Sep 2022 (actual)
- Primary completion
- 1 Dec 2022 (estimated)
- Study completion
- 1 Feb 2023 (estimated)
- First posted
- 13 Oct 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Because of the shortage of doctors in France, notably gynaecologist, general practitioners are definitely an essential partner women's health. However, few of them regularly practice gynecological acts.
A lot of studies have studied why general doctors not practice gynecological acts but it would necessary to include the women's perspective.
Detailed description
The aim of the study will be identify women's factors associated with gynaecological consultation by the general practitioner.
Study design
- Observational model
- Case only
- Time perspective
- Cross-sectional
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- women aged more than 18 years old, who consent to participle to the study
Key inclusion criteria (2 listed)
- women aged more than 18 years old
- woman agreeing to participate to the study
Key exclusion criteria (2 listed)
- women aged less than 18 years old
- woman not agreeing to participate to the study
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| " women group "women aged more than 18 years old | Other | – |
Primary outcome
Acceptance of gynecological consultation with a general practitioner
Time frame: Day 0
would the woman agree to consult a general practitioner for a gynecological reason ? (Yes or No)
1 secondary outcome
Women's knowledge of general practitioner gynecology competences
Time frame: Day 0
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Oct 2022.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
barbe coralie principal investigator
pratictioner
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Adult Daughters, run by Université de Reims Champagne-Ardenne at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 18 Oct 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact coralie barbe (326913665 ext. +33, cbarbe1@univ-reims.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Acceptance of gynecological consultation with a general practitioner (time frame: Day 0). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Oct 2022.