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Distress in Crisis Situations During COVID-19

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04337047
Recruitment Status : Completed
First Posted : April 7, 2020
Last Update Posted : May 5, 2020
Sponsor:
Information provided by (Responsible Party):
benjamin CHAIX, Wefight

Brief Summary:

There are many scales for screening or assessing the impact of a disease. These scales are generally used to diagnose or assess the severity of a disease and are carried out at the request of a physician by the patient. Conversational agents could make it possible to administer these questionnaires remotely, analyse them and use the results on a large scale, without prior medical intervention.

The main objective of this study is to quantify and qualify the distress of a large population in times of pandemic crisis.


Condition or disease Intervention/treatment
Stress, Psychological Other: questionnaire assesment

Detailed Description:

The Peritraumatic Distress Inventory is the standard tool designed to assess distress in times of crisis. It consists of 13 questions.

Questions will be submitted to the participants from the Vik chatbot. Responses will be analysed and compared according to the demographics and pathologies encountered.

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Study Type : Observational
Actual Enrollment : 2000 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Distress During the COVID-19 Pandemic in France: a National Assessment of At-risk Populations
Actual Study Start Date : March 31, 2020
Actual Primary Completion Date : April 30, 2020
Actual Study Completion Date : May 3, 2020

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Stress

Group/Cohort Intervention/treatment
Vik sein
Vik sein users
Other: questionnaire assesment
questionnaire assesment

Vik asthme
Vik asthme users
Other: questionnaire assesment
questionnaire assesment

Vik migraine
Vik migraine users
Other: questionnaire assesment
questionnaire assesment

Vik depression
Vik depression users
Other: questionnaire assesment
questionnaire assesment




Primary Outcome Measures :
  1. quantify and qualify distress over a large population in times of pandemic crisis. [ Time Frame: 1 month ]

Secondary Outcome Measures :
  1. qualify demographic data vs distress over a large population in times of pandemic crisis. [ Time Frame: 1 month ]


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
Vik's users in France
Criteria

Inclusion Criteria:

  • Age > 18 years old

    • Collection of the subject's non-opposition
    • Patient registration on Vik breast, Vik asthma, Vik migraine, Vik depression

Exclusion Criteria:

  • Patient unable to formulate non-opposition

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04337047


Locations
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France
Wefight
Montpellier, France, 34000
Sponsors and Collaborators
Wefight
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Responsible Party: benjamin CHAIX, Chief Science Officer, Wefight
ClinicalTrials.gov Identifier: NCT04337047    
Other Study ID Numbers: WefightDistress20
First Posted: April 7, 2020    Key Record Dates
Last Update Posted: May 5, 2020
Last Verified: May 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Stress, Psychological
Behavioral Symptoms