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Feasibility and Acceptability Study of the O'Dide Application in People Suffering From an Addiction

Feasibility and Acceptability Study of the O'Dide Application in People Suffering From an Addiction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04659954
Acronym
FA-O'DIDE
Enrollment
24
Registered
2020-12-09
Start date
2022-01-07
Completion date
2023-02-10
Last updated
2023-12-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Personality Disorders, Substance-Related Disorders

Keywords

E health, Application, Substance use disorders, Personality disorders, Care observance

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. With the present study, the investigator 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.

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.

Interventions

OTHERApplication 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.

Sponsors

Institut de Recherche en Santé Publique, France
CollaboratorOTHER
University Hospital, Toulouse
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Suffering from any type of addiction, with an active addiction requiring weekly monitoring of consumption * Possessing an Android smartphone or having access to an Android smartphone and having access to an internet connection * Able to read and understand French * Affiliated or beneficiary of a social security scheme. * 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

* Patient with cognitive or psychiatric disorders that may affect their ability to consent * Participation in another protocol involving a modification of the treatment for addiction * Person under legal protection, guardianship or curatorship * Known or suspected pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of use of the application O'DIDE during 8 weeks8 weeksPercentage of patients who logged on at least once a week to the application during the 8 weeks of availability of the O'DIDE application

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026