FA-O'DIDE: Feasibility and Acceptability Study of the "O'Dide" Application in People Suffering From an Addiction
Study Details
Study Description
Brief Summary
Substance Use Disorders (SUD) are associated with cognitive schemas that lead to care attrition and mistrust towards care. Considering this within SUD management, it is important to establish a confident relation between the patient and the care team to favorize acre observance. However, it demands an important availability of the healthcare team, allowing for frequent interactions at all times, including at night and during days off. We postulated that an application called Ô DIDE for Digital Interaction for Detoxification Engagement, that aims to help the caregivers maintaining a link with the patient in order to facilitate confidence in the relationship, could favorize care observance especially consumption report.
Condition or Disease | Intervention/Treatment | Phase |
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N/A |
Detailed Description
The present research aims to assess the feasibility of the "Ô DIDE" application after 8 weeks of use by patients treated for a disorder related to substance use at the Toulouse University Hospital.
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
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Experimental: Application O'DIDE The subjects will use the application O'DIDE during 8 weeks |
Other: Application O'DIDE
The intervention is the use of an application that aimed to favorize contact between the patient and the care team between the consultations.
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Outcome Measures
Primary Outcome Measures
- Feasibility of the application O'DIDE [8 weeks]
Percentage of patients who logged on at least once a week to the application during the 8 weeks of availability of the O'DIDE application
Eligibility Criteria
Criteria
Inclusion Criteria:
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Suffering from any type of addiction, with an active addiction requiring weekly monitoring of consumption
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Possessing an Android smartphone or having access to an Android smartphone and having access to an internet connection
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Able to read and understand French
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Affiliated or beneficiary of a social security scheme.
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Free, informed and written consent signed by the participant and the investigator (at the latest on the day of inclusion and before any examination required by the research).
Exclusion Criteria:
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Patient with cognitive or psychiatric disorders that may affect their ability to consent
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Participation in another protocol involving a modification of the treatment for addiction
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Person under legal protection, guardianship or curatorship
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Known or suspected pregnancy
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
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1 | University hospital of Toulouse | Toulouse | France | 31059 |
Sponsors and Collaborators
- University Hospital, Toulouse
- Institut de Recherche en Santé Publique, France
Investigators
- Principal Investigator: Juliette Salles, MD, University Hospital, Toulouse
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- RC31/20/0367