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Feasibility and Acceptability Study of the "O'Dide" Application in People Suffering From an Addiction (FA-O'DIDE)

T

Toulouse University Hospital

Status

Completed

Conditions

Substance-Related Disorders
Personality Disorders

Treatments

Other: Application O'DIDE

Study type

Interventional

Funder types

Other

Identifiers

NCT04659954
RC31/20/0367

Details and patient eligibility

About

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.

Full 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.

Enrollment

24 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

24 participants in 1 patient group

Application O'DIDE
Experimental group
Description:
The subjects will use the application O'DIDE during 8 weeks
Treatment:
Other: Application O'DIDE

Trial contacts and locations

1

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Central trial contact

Juliette Salles, MD

Data sourced from clinicaltrials.gov

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