- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03875586
Consultation Reasons in Family Medicine (EMOCONSULT)
August 21, 2019 updated by: Dacima Consulting
EMOCONSULT : Consultation Reasons in Family Medicine, a Tunisian National Survey
The Tunisian society of family medicine STMF proposes to coordinate a national, observational, transversal and multicenter survey, at the consultations of general medicine / family medicine.
Study Overview
Status
Completed
Detailed Description
The Tunisian society of family medicine STMF proposes to coordinate a national, observational, transversal and multicenter survey carried out during two weeks, at the consultations of general medicine / family medicine.
The main objective of the survey is to describe the reasons for consultation in general medicine / family medicine.
The results obtained from this survey will make it possible to specify the specificities inherent to the reasons for consultations of Tunisians but especially to the peculiarities of the local health system (public and private).
This survey will help us to assimilate our practices and harmonize them in order to optimize patient care and reposition family medicine in the patient's care path as well as the degree of adherence of practitioners to international recommendations in the care of the patient.
Study Type
Observational
Enrollment (Actual)
10822
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
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-
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Tunis, Tunisia, 2092
- STMF - Société Tunisienne de Médecine de Famille
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Tunis, Tunisia
- DACIMA
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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 to 95 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
All patients consulting in general medicine / family medicine.
Description
Inclusion Criteria:
- Age ≥ 18 years
- Informed consent, read and signed
Exclusion Criteria:
• Consent not obtained
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 |
|---|---|---|
|
Describe the reasons for consultation in family medicine / general medicine
Time Frame: 2 weeks
|
All patients presenting in consultation in general medicine / family medicine will be recruited in the survey in order to describe the different reasons for consultation
|
2 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Chair: Maha Ben Moallem Hachicha, MD, STMF
- Study Chair: Zied Ben Lamine, MD, STMF
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
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)
April 29, 2019
Primary Completion (Actual)
May 16, 2019
Study Completion (Actual)
May 16, 2019
Study Registration Dates
First Submitted
March 13, 2019
First Submitted That Met QC Criteria
March 13, 2019
First Posted (Actual)
March 15, 2019
Study Record Updates
Last Update Posted (Actual)
August 26, 2019
Last Update Submitted That Met QC Criteria
August 21, 2019
Last Verified
August 1, 2019
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- DAC-005-EMOCONSULT
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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