digital behavioral intervention: interaction with a conversational agent to implement physical and cognitive programs
Study summary
KANOPEE is a free smartphone application providing screening, follow-up tools and autonomous digital interventions to lower psycho-social stress and its repercussions on sleep and behaviors in the general population.
Additionally, KANOPEE permits an adaptation of the intervention to the subject (i.e., an adapted waiting period, frequency, and content), enabling to perform innovative trial conditions.
The objective of this long-term study is to evaluate the efficacy of KANOPEE on users among the French general population exposed to psycho-social stress.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria:
* Being aged 18 years old and over (the app is available for younger users but their data will not be analyzed)
* having downloaded the app
* having a smartphone Android or Iphone
* being located in France
* having accepted the electronic informed consent
Exclusion Criteria:
* having clicked on the "emergency button" (in the app, there is a warning message : this app is not for emergency situations. If you need an urgent psychological support, click here")
* having downloaded the app but without answering any questionnaire
Primary outcome measure(s)
Sleep complaints — weekly, from the downloading of the app until two weeks after the end of the intervention measured by the Insomnia Severity Index (ISI), total score ranging from 0 to 28, higher score indicating higher sleep complaint.
Fatigue complaints — weekly, from the downloading of the app until two weeks after the end of the intervention measured by the Fatigue Severity Scale (FSS), total score ranging from 1 to 7, higher score indicating higher perceived fatigue.
Depression and anxiety complaints — weekly, from the downloading of the app until two weeks after the end of the intervention measured by the Patient Health Questionnaire 4 items (PHQ-4), total score ranging from 0 to 12, higher scores indicating higher depression or anxiety complaints.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
We use cookies to analyse site traffic and improve your experience. With your consent, we may also use cookies for advertising. You can change your choice at any time.