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Completed

NCT Number: NCT04659954

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

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.

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Key information

Conditions

Substance-related Disorders Chemically-Induced Disorders Mental Disorders Personality Disorders

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University hospital of Toulouse

Toulouse, 31059, France

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Application O'DIDE

Other

The intervention is the use of an application that aimed to favorize contact between the patient and the care team between the consultations.

Primary outcomes

  1. Feasibility of use of the application O'DIDE during 8 weeks

    Time frame: 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

Sponsors and collaborators

Lead sponsor

University Hospital, Toulouse

Other

Collaborators

  • Institut de Recherche en Santé Publique, France

Registry information

Acronym: FA-O'DIDE

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Dec 9, 2020
Registry last updated
Dec 19, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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