- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05788731
Become of Patients From the Permanent Access to Care (PASS) in Cayenne, French Guyana, Suffering From a Chronic Disease (High Blood Pressure - Diabetes) in the Common Law Schemes (PASSyDroit)
March 27, 2023 updated by: Centre Hospitalier de Cayenne
It is an observational research, conducted at the Cayenne hospital about the future of hypertensive and/or diabetic patients after their follow-up at the Permanent Access to care (PASS).
The PASS is a medico-social structure that allows access to medical monitoring and support towards common law.
The main objective of the study is to evaluate the use of the common law system by these patients.
Then the goal is to study the relationship between integration into the system and socio-demographic, medical characteristics, and understanding of health monitoring.
Data will be collected by guided telephone interviews and the review of medical records.
Study Overview
Status
Completed
Detailed Description
The problems of social inequalities in access to care are major public health issues as recalled by the Regional Health Agency (ARS) of French Guiana in the Regional Health Project (PRS).
French Guiana has high precariousness indicators with half of its population living below the poverty line.
In addition, health indicators are often more degraded in precarious populations.
Thus, in French Guiana, there is a higher rate of premature mortality, partly attributable to obesity, sedentary lifestyle, diabetes and hypertension than in mainland France.
Despite an increased need for follow-up of chronic pathologies, the precarious population faces many difficulties in accessing care.
The Permanent Access to Health Care (PASS) in Cayenne is a medico-social system, created to respond to these problems.
The PASS allows access to monitoring of chronic diseases and support towards the common law healthcare system.
Although the phenomenon of non-use of care studied in the precarious population of western French Guiana seems primarily attributable to the absence of social security.
The main objective is to evaluate the use of the common law system in hypertensive or diabetic patients treated at the PASS in Cayenne.
In addition, the investigators want to study the relationship between integration into the system and the socio-demographic, medical characteristics, understanding of health monitoring.
Study Type
Observational
Enrollment (Actual)
120
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
-
-
-
Cayenne, French Guiana, 97306
- Centre Hospitalier de Cayenne
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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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Majeur patients of the PASS of CH de Cayenne with a chronic disease
Description
Inclusion Criteria:
- Be 18 years or older
- Past follow-up by the PASS of the Cayenne hospital for at least one chronic pathology identified as follows: hypertension, diabetes.
- The discharge and reorientation to general practitioner have happened between 1 month and 1 year prior to this study.
Exclusion Criteria:
- Patient with a psychiatric condition
- Refusing the study
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 |
|---|---|---|
|
The proportion of patients integrating the common law system
Time Frame: during inclusion
|
It is collected through telephone interviews while inclusions are carried out.
|
during inclusion
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Study the relationship between system integration and socio-demographic, understanding characteristics
Time Frame: during inclusion
|
during inclusion
|
|
Study the relationship between system integration and medical, health follow-up
Time Frame: during inclusion
|
during inclusion
|
|
Proportion of patients resorting to one or more consultations with a general practitioner.
Time Frame: during inclusion
|
during inclusion
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
- Projet Régional de Santé (PRS) Guyane 2018-2028
- Samuel A, Vianney C. Les maladies chroniques touchent plus souvent les personnes modestes et réduisent davantage leur espérance de vie | Direction de la recherche, des études, de l'évaluation et des statistiques
- Nacher M. santé globale et guyane: étude descriptive et comparative de quelques grands indicateurs / global health and french guiana: a descriptive and comparative study of some major indicators. 24 juin 2019;10.
- Legendre B. Le renoncement aux soins : un phénomène aux ressorts économiques mais aussi sociaux. Rev Fr Aff Soc. 2021;(3):179-204.
- Kieffer M. PrecASOG : Accès aux soins dans l'Ouest Guyanais : étude des causes de rupture thérapeutique chez les patients précaires atteints de maladie chronique. Université des Antilles; 2022
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 18, 2023
Primary Completion (Actual)
February 28, 2023
Study Completion (Actual)
February 28, 2023
Study Registration Dates
First Submitted
March 8, 2023
First Submitted That Met QC Criteria
March 27, 2023
First Posted (Actual)
March 29, 2023
Study Record Updates
Last Update Posted (Actual)
March 29, 2023
Last Update Submitted That Met QC Criteria
March 27, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PASSyDroit
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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.