NCT04494854

Brief Summary

The aim of this study is to analyze the perceptions, representations and expe-riences of malaria prophylaxis in patients born in endemic areas and living in France. This analysis could lead to better understanding and communication between the medical profession and patients in malaria. It would also provide patient-specific responses to their expectations, as to their families.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
15

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Sep 2020

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 17, 2020

Completed
14 days until next milestone

First Posted

Study publicly available on registry

July 31, 2020

Completed
1 month until next milestone

Study Start

First participant enrolled

September 1, 2020

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2020

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2020

Completed
Last Updated

June 7, 2023

Status Verified

June 1, 2023

Enrollment Period

1 month

First QC Date

July 17, 2020

Last Update Submit

June 6, 2023

Conditions

Keywords

perception, representation, experience, questionnaire

Outcome Measures

Primary Outcomes (1)

  • Identify perceptions, representations and experiences of malaria prophylaxis in patients coming from endemic areas living in France.

    The semi directive interview

    Through study completion, an average of 30 minutes

Secondary Outcomes (1)

  • Identification of dialogue tools allowing a better relationship of trust between doctor and patient within the framework of a prevention consultation, and better delivery of key information

    Through study completion, an average of 30 minutes

Eligibility Criteria

Age18 Months+
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study will be offered to patients born in endemic areas and living in France.

You may qualify if:

  • Major patients
  • Born in malaria endemic areas and living in France
  • Having malaria or not
  • Ready for no opposition for participation in the protocol

You may not qualify if:

  • Patients under guardianship or curatorship
  • Patients unable to give free and informed consent
  • Patients under judicial protection

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre hospitalier intercommunal de Villeneuve St Georges

Villeneuve-Saint-Georges, 94190, France

Location

MeSH Terms

Conditions

MalariaCommunicable DiseasesTravel-Related Illness

Condition Hierarchy (Ancestors)

Protozoan InfectionsParasitic DiseasesInfectionsMosquito-Borne DiseasesVector Borne DiseasesDisease AttributesPathologic ProcessesPathological Conditions, Signs and SymptomsSigns and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 17, 2020

First Posted

July 31, 2020

Study Start

September 1, 2020

Primary Completion

October 1, 2020

Study Completion

November 1, 2020

Last Updated

June 7, 2023

Record last verified: 2023-06

Locations