- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03886285
A Quality Rating Scale for Patients in Complex Situations (Qualsoprim_2)
Establish a Scale of Assessment of the Quality of Primary Care in Multi-functional Health Centers and Homes Integrating the Point of View of Complex Patients and Their Caregivers
The prevalence of multimorbid patients and complex care is increasing in France and elsewhere in the world. It concerns 60% of the over 65 years old. Comprehensive care, the involvement of the patient and his caregivers appear as the solutions for the management of these new care situations. The structures of multi-professional grouping, developing a coordinated exercise (GECO), appear as the privileged place to take care of these patients. These structures become the main place of exercise in France (improved working conditions for professionals, financial incentives, public policy, etc.); they have shown their ability to formulate patient care protocols, to produce coordinated exercise, to better involve the patient and caregivers in their care. The question of improving the quality of care arises. To date, there is no data on the subject apart from some evaluations mainly medico-economic.
The patient's place in the evaluation showed his interest with the existence of a proven correlation between patient satisfaction in particular and his compliance and health outcomes.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Audierne, France, 29770
- Maison de santé d'Audierne
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Cavan, France, 22140
- Maison de santé de CAVAN
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Gourin, France, 56110
- Maison de santé de Gourin
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Lanmeur, France, 29620
- Pôle de santé de Lanmeur
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Le Faou, France, 29590
- Maison de santé du Faou
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Le Vieux Marche, France, 22420
- Maison de santé du Vieux Marché
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Louargat, France, 22540
- Maison de santé de LOUARGAT
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Milizac, France, 29290
- Maison de santé de Milizac
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Moëlan-sur-Mer, France, 29350
- Maison de santé de Moëlan sur Mer
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Pleyben, France, 29190
- Maison de santé de Pleyben
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Plouneour Trez, France, 29890
- Maison de santé de Plouneour Trez
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Trebeurden, France, 22560
- Maison de santé de Trébeurden
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patient followed in the primary care center, able to participate, speaking and understanding French, and being in a complex care situation, benefiting from a multi-professional care (at least two professionals different from the center including the general practitioner).
Exclusion Criteria:
- Patient not in a complex care situation
- Patient followed only by the general practitioner of GECO
- Refusal of participation
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Construction of the questionnaire.
Time Frame: 1 day
|
The main objective of this phase of the protocol is to structure the questionnaire in order to achieve a scale of assessment of the quality of primary care provided within the coordinated exercise groups from the point of view of complex care patients, their caregivers and patients and health professionals.
This questionnaire doesn't exist so it has no name.This questionnaire is qualitative and not quantitative, so nos score is expected.
|
1 day
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 29BRC19.0019
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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