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A Phone-call With a Student/General Practitioner Team to Impact Morbidity of Chronic Patients During COVID-19 Containment (COVIQuest)

Primary Purpose

Cardiovascular Diseases, Mental Disorder

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Phone-call screening and management by a medical student/general practitioner tandem
Sponsored by
University Hospital, Tours
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Cardiovascular Diseases focused on measuring general practice, COVID-19, chronic diseases, medical student

Eligibility Criteria

18 Years - 110 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria (patient with a chronic cardiovascular) :

  • Male or female
  • >= 70 years of age
  • Participants covered by or entitled to social security
  • With a chronic cardiovascular or mental disease as referenced in the long term illness (ALD) list (i.e. with an ALD n°1, 3, 5, 12, 13 for cardiovascular disease)
  • Followed regularly by their general practitioner (i.e. entered in the list of patients followed by a general practitioner by French Health Insurance
  • Participants who has given oral, express and informed consent.

Inclusion criteria (patient with a mental disease) :

  • Male or female
  • >= 18 years of age
  • Participants covered by or entitled to social security
  • With a chronic cardiovascular or mental disease as referenced in the long term illness (ALD) list (i.e. with an ALD 23 for mental disease)
  • Followed regularly by their general practitioner (i.e. entered in the list of patients followed by a general practitioner by French Health Insurance
  • Participants who has given oral, express and informed consent

Exclusion criteria :

  • Patients with both a cardiovascular ALD and a mental health ALD (they will benefit from the intervention, without participating in the trial)
  • Patients already and directly managed by their general practitioner during containment and whose general practitioner refuses that the patient be contacted by someone other than himself
  • Patients unable to provide informed consent.

Sites / Locations

  • Dibao-Dina

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Management by a student/general practitioner tandem

Usual care

Arm Description

Patients will receive a phone call from the medical student who will inquire about their health. The medical student will then transmit this information to the general practitioner who will decide on the most suitable management for the patient.

Usual care, i.e. patients will call their general practitioner when needed, up to 1 month, which corresponds to the estimated time for the intervention to be delivered to all patients in the intervention group. At the end of the intervention at 1 month, patients in the usual care group will also receive a phone-call from the medical student/general practitioner tandem.

Outcomes

Primary Outcome Measures

Hospitalization(s) at 1 month
Hospitalization over a one month period. The primary outcome will be collected by a phone call from a medical student to the patient 1 month after randomization date. Hospitalizations (date, location, length, if available, and reason) will be collected. Because there will be many patients to be called for each practitioner, we expect these phone call to occur within a few days after day 28.

Secondary Outcome Measures

Phone-call from the general practitioner (in the experimental group only)
In the experimental group only: proportion of patients for whom the practitioner had to call back after the medical student had phoned (just after allocation of the practice to the experimental group) at 1 month.
Mortality at 1 month
Mortality will be reported after checking with the city of the patient's home if there is no response to the phone call
Use of primary care
Number of general practitioner consultations and teleconsultations (and time of general practitioner consultation, i.e. during the containment period or not) using data from the French Health National (SNDS) Database
Use of secondary care
Number of consultations with another medical specialist (and time of consultation, i.e. during the containment period or not) using data from the French Health National (SNDS) Database
Number of prescriptions related to the chronic disease dispensed by the pharmacy
Number of prescriptions related to the chronic disease that were dispensed by the pharmacy using data from the French Health National (SNDS) Database
Number of hospitalization(s)
Number of hospitalizations using data from the French Health National (SNDS) Database
Time to hospitalization(s)
Time to hospitalization using data from the French Health National (SNDS) Database
Hospitalization(s)' durations
Hospitalization duration using data from the French Health National (SNDS) Database
Reasons for hospitalization(s)
Reason for hospitalization using data from the French Health National (SNDS) Database
Mortality at 6 months
Number of deaths using data from the French Health National (SNDS) Database
Cardiovascular events (MACE)
Only for patients in the COVIQuest_CV sub-trial: Cardiovascular events (MACE): nonfatal stroke, nonfatal myocardial infarction, cardiovascular death and hospitalization for heart failure using data from the French Health National (SNDS) Database
Psychotropic drugs
Only for patients in the COVIQuest_MH sub-trial: Psychotropic drugs consumption using data from the French Health National (SNDS) Database

Full Information

First Posted
April 18, 2020
Last Updated
April 7, 2021
Sponsor
University Hospital, Tours
Collaborators
INSERM CIC-P 1415
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1. Study Identification

Unique Protocol Identification Number
NCT04359875
Brief Title
A Phone-call With a Student/General Practitioner Team to Impact Morbidity of Chronic Patients During COVID-19 Containment
Acronym
COVIQuest
Official Title
Does a Systematic Phone-call by a Medical Student/General Practitioner Team in Patients Suffering From a Chronic Condition During the COVID-19 Containment Period Impact One-month Hospitalization's Rate in France? A Cluster Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
April 30, 2020 (Actual)
Primary Completion Date
June 30, 2020 (Actual)
Study Completion Date
December 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Tours
Collaborators
INSERM CIC-P 1415

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Following the announcement of the containment of the population due to the COVID-19 epidemic on March 17, 2020 in France, a notable decrease in the number of consultations in general practice was reported. Patients no longer contact their general practitioner, including those with regular follow-up for one or more chronic conditions. This observation raised worries since it could lead to delay or failure in detecting decompensations / complications of these chronic conditions by a lack of recourse to care. Thus, an urgent message from the National Health Department (Direction Générale de la Santé - DGS) was adressed on April 8, 2020 to the health professionals regarding the organization of care aside from COVID-19. The main recommendation was "that the personal physician or the corresponding specialist should contact the most fragile patients with chronic condition to ensure follow-up and detect any risk of decompensation ". Such fragile patients are in great numbers, up to more than 200 for an average general practitioner. Therefore, although this recommendation is regarded as "essential in view of the health needs of the population", it will prove quite difficult to follow without the help of a skilled external assistance that can be quickly mobilized.
Detailed Description
Following the announcement of the containment of the population due to the COVID-19 epidemic on March 17, 2020 in France, a notable decrease in the number of consultations in general practice was reported. Patients no longer contact their general practitioner, including those with regular follow-up for one or more chronic conditions. This observation raised worries since it could lead to delay or failure in detecting decompensations / complications of these chronic conditions by a lack of recourse to care. Thus, an urgent message from the National Health Department (Direction Générale de la Santé - DGS) was adressed on April 8, 2020 to the health professionals regarding the organization of care aside from COVID-19. The main recommendation was "that the personal physician or the corresponding specialist should contact the most fragile patients with chronic condition to ensure follow-up and detect any risk of decompensation ". Such fragile patients are in great numbers, up to more than 200 for an average general practitioner. Therefore, although this recommendation is regarded as "essential in view of the health needs of the population", it will prove quite difficult to follow without the help of a skilled external assistance that can be quickly mobilized. The COVIQUEST project is a cluster randomized trial in general practice designed to assess the optimizationg of the screening and management of patients with chronic condition at risk of decompensation through a collaboration between the general practitioner and a medical student. The trial will focus on patients wit cardiovascular conditions aged 70 or more and patients with mental health conditions. These conditions are both highly prevalent in general practice and both at risk of severe short-term complications. Practices will be randomly assigned to a group (A or B). In group A, students will start by contacting patients with cardiovascular conditions; in group B they will start by contacting patients patients with mentral health conditions. The students will call these patients on the phone and ask them specific questions about their health, their needs, and if they want their general practitioner to call them back. The student will then transmit this information to the general practitioner who will decide on the best care to offer the patient. The primary outcome is defined as the occurrence of hospitalization during a one-month period after the phone call. It will be collected by a second phone call from the medical student. This time, all patients will be contacted, i.e. both patients with mental illness and cardiovascular patients, whatever the group. Thus, patients allocated to the control groups (i.e. patients with mental illness from group A and cardiovascular patients from group B) will also benefit from the intervention at 1 month: again, students will ask patients about their health and whether they want their general practitioner to call them back. This approach has several advantages: all patients will benefit from a phone call, in accordance with the recommendations of the DGS, the involvement of students, competent in medical interviews and quickly mobilizable, will help general practitioners, on the front line of many missions, without any health risk linked to the contagiousness of COVID-19 for students, randomizing the call order will allow to assess with a high level of evidence the impact of such an organization on hospitalizations, for two families of diseases with high prevalence. The trial will involve at least nine French regions. Considering that the general practitioner's patient base numbers an average of 110 patients with chronic cardiovascular disease or chronic mental illness, and that at least 25 general practitioners per region participate in the study, we can expect that 22,000 patients will benefit from the intervention of this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Diseases, Mental Disorder
Keywords
general practice, COVID-19, chronic diseases, medical student

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Cluster randomized trial with 2 subtrials : COVIQuest_CV and COVIQuest_MH. COVIQuest_CV involves patients ≥ 70 years old suffering from chronic cardiovascular disease; and COVIQuest_MH involves patients suffering from a mental health disease. As a note, both sub-trials are two-parallel group cluster randomized trials. Clusters will be defined as practices. Practices will be randomized into two groups A and B. For practices in group A: their CV patients constitute the experimental group for the COVIQuest_CV trial, their MH patients constitute the control group for the COVIQuest_MH trial. For practices in group B: their CV patients constitute the control group for the COVIQuest_CV trial, their MH patients constitute the experimental group for the COVIQuest_MH trial.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
22000 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Management by a student/general practitioner tandem
Arm Type
Experimental
Arm Description
Patients will receive a phone call from the medical student who will inquire about their health. The medical student will then transmit this information to the general practitioner who will decide on the most suitable management for the patient.
Arm Title
Usual care
Arm Type
No Intervention
Arm Description
Usual care, i.e. patients will call their general practitioner when needed, up to 1 month, which corresponds to the estimated time for the intervention to be delivered to all patients in the intervention group. At the end of the intervention at 1 month, patients in the usual care group will also receive a phone-call from the medical student/general practitioner tandem.
Intervention Type
Behavioral
Intervention Name(s)
Phone-call screening and management by a medical student/general practitioner tandem
Intervention Description
Systematic phone contact of the patient by a medical student, under the indirect supervision of the general practitioner. This phone contact will be standardized with 3 questions to ask to the patient: How are you doing? (with a Likert scale from 1=very bad to 10=very well) Would you have made an appointment with your general practitioner if there had not been COVID19 epidemic and containment? Would you like an appointment with your doctor and / or has your doctor ever contacted you? In view of the answers to these 3 questions, the general practitioner will decide whether it is necessary to propose a consultation or a teleconsultation to the patient, taking into account his/her medical background.
Primary Outcome Measure Information:
Title
Hospitalization(s) at 1 month
Description
Hospitalization over a one month period. The primary outcome will be collected by a phone call from a medical student to the patient 1 month after randomization date. Hospitalizations (date, location, length, if available, and reason) will be collected. Because there will be many patients to be called for each practitioner, we expect these phone call to occur within a few days after day 28.
Time Frame
1 month
Secondary Outcome Measure Information:
Title
Phone-call from the general practitioner (in the experimental group only)
Description
In the experimental group only: proportion of patients for whom the practitioner had to call back after the medical student had phoned (just after allocation of the practice to the experimental group) at 1 month.
Time Frame
1 month
Title
Mortality at 1 month
Description
Mortality will be reported after checking with the city of the patient's home if there is no response to the phone call
Time Frame
1 month
Title
Use of primary care
Description
Number of general practitioner consultations and teleconsultations (and time of general practitioner consultation, i.e. during the containment period or not) using data from the French Health National (SNDS) Database
Time Frame
6 months
Title
Use of secondary care
Description
Number of consultations with another medical specialist (and time of consultation, i.e. during the containment period or not) using data from the French Health National (SNDS) Database
Time Frame
6 months
Title
Number of prescriptions related to the chronic disease dispensed by the pharmacy
Description
Number of prescriptions related to the chronic disease that were dispensed by the pharmacy using data from the French Health National (SNDS) Database
Time Frame
6 months
Title
Number of hospitalization(s)
Description
Number of hospitalizations using data from the French Health National (SNDS) Database
Time Frame
6 months
Title
Time to hospitalization(s)
Description
Time to hospitalization using data from the French Health National (SNDS) Database
Time Frame
6 months
Title
Hospitalization(s)' durations
Description
Hospitalization duration using data from the French Health National (SNDS) Database
Time Frame
6 months
Title
Reasons for hospitalization(s)
Description
Reason for hospitalization using data from the French Health National (SNDS) Database
Time Frame
6 months
Title
Mortality at 6 months
Description
Number of deaths using data from the French Health National (SNDS) Database
Time Frame
6 months
Title
Cardiovascular events (MACE)
Description
Only for patients in the COVIQuest_CV sub-trial: Cardiovascular events (MACE): nonfatal stroke, nonfatal myocardial infarction, cardiovascular death and hospitalization for heart failure using data from the French Health National (SNDS) Database
Time Frame
6 months
Title
Psychotropic drugs
Description
Only for patients in the COVIQuest_MH sub-trial: Psychotropic drugs consumption using data from the French Health National (SNDS) Database
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
110 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria (patient with a chronic cardiovascular) : Male or female >= 70 years of age Participants covered by or entitled to social security With a chronic cardiovascular or mental disease as referenced in the long term illness (ALD) list (i.e. with an ALD n°1, 3, 5, 12, 13 for cardiovascular disease) Followed regularly by their general practitioner (i.e. entered in the list of patients followed by a general practitioner by French Health Insurance Participants who has given oral, express and informed consent. Inclusion criteria (patient with a mental disease) : Male or female >= 18 years of age Participants covered by or entitled to social security With a chronic cardiovascular or mental disease as referenced in the long term illness (ALD) list (i.e. with an ALD 23 for mental disease) Followed regularly by their general practitioner (i.e. entered in the list of patients followed by a general practitioner by French Health Insurance Participants who has given oral, express and informed consent Exclusion criteria : Patients with both a cardiovascular ALD and a mental health ALD (they will benefit from the intervention, without participating in the trial) Patients already and directly managed by their general practitioner during containment and whose general practitioner refuses that the patient be contacted by someone other than himself Patients unable to provide informed consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
CLARISSE DIBAO-DINA, MD-PhD
Organizational Affiliation
University Hospital of TOURS
Official's Role
Study Director
Facility Information:
Facility Name
Dibao-Dina
City
Tours
ZIP/Postal Code
37000
Country
France

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
One-month-data can be shared, whereas 6-month data are not legally sharable (electronic health records).
IPD Sharing Time Frame
1 year
IPD Sharing Access Criteria
email
Citations:
PubMed Identifier
35902188
Citation
Dibao-Dina C, Leger J, Ettori-Ajasse I, Boivin E, Chambe J, Abou-Mrad-Fricquegnon K, Sun S, Jego M, Motte B, Chiron B, Sidorkiewicz S, Khau CA, Bouchez T, Ghali M, Bruel S, Lebeau JP, Camus V, El-Hage W, Angoulvant D, Caille A, Guillon-Grammatico L, Laurent E, Saint-Lary O, Boussageon R, Pouchain D, Giraudeau B; COVIQuest group. Impact of a phone call with a medical student/general practitioner team on morbidity of chronic patients during the first French COVID-19 lockdown (COVIQuest): a cluster randomised trial. BMJ Open. 2022 Jul 28;12(7):e059464. doi: 10.1136/bmjopen-2021-059464.
Results Reference
derived

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A Phone-call With a Student/General Practitioner Team to Impact Morbidity of Chronic Patients During COVID-19 Containment

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