CORVI: Benefits of Therapy With Virtual Reality Exposure in the Treatment of Cocaine Use Disorders

Sponsor
University Hospital, Clermont-Ferrand (Other)
Overall Status
Unknown status
CT.gov ID
NCT04280900
Collaborator
Fondation de l'Avenir, France (Other)
50
1
2
19
2.6

Study Details

Study Description

Brief Summary

Cocaine addiction is a multifactorial disease with important consequences: somatic, psychiatric... The number of applications for treatment for cocaine addiction is gradually increasing from year to year but no conventional treatment is available. New tools such as virtual reality could be used in this treatment. We propose to create a virtual reality program based on the analysis of high-risk relapse situations described by patients. We will then assess the effect of this cybertherapy on patients' relapse time and their desire to use cocaine

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Virtual Reality-Enhanced Cognitive Behavioral Therapy (VR-CBT)
  • Behavioral: Treatment as usual
N/A

Detailed Description

In France, according to the Health Barometer 2017, cocaine testing has seen two decades of increases from 1.2% in 1995 to 5.6% in 2017, making it the second most widely used illicit substance. About 5% of cocaine users may become addicted in the first year of use, while 20% will develop long-term addiction. This dependence or substance use disorder is characterized in particular by a loss of control of cocaine use and continued use despite the negative consequences. Another of the central dimensions of this disorder is the craving (irresistible or irrepressible need or desire to consume) which is caused by internal or external stimuli. Craving is the cause of frequent loss of controls and re-consumption.

The treatment of cocaine addictions is generally based on a dual model of pharmacological treatment often aimed at limiting craving and psychotherapeutic treatment in order to alter the emotions and memory associated with cocaine use; for example: relearning product management when it comes to the subject.

In this context, the use of a 3D tool, which allows a gradual and well-detested exposure without confrontation, seems an interesting prospect. Virtual reality therapies have historically been known for treating phobias (fears). In addictions, exposure therapies are done in imagination and rarely with consumer-inducing situations. Since 2000, several researchers have successfully used virtual reality applications in addictions, but there is little data on objective assessments of the effectiveness of cybertherapy in the treatment of cocaine addictions.

All of these elements converge to propose a protocol called "CORVI" to evaluate the effectiveness of virtual reality exposure therapy as the management of patients with cocaine use disorder versus management classic.

The project is based on 3 phases: 1/construction of films that can be used in cybertherapy that reproduce situations in which there are stimuli generating "craving" to cocaine. 2/ Treatment of 2 randomized patient groups with and without cybertherapy (n-20/group) 3/Relapse evaluations at 1.2 and 3 months post-treatment

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Benefits of Therapy With Virtual Reality Exposure in the Treatment of Cocaine Use Disorders
Anticipated Study Start Date :
Jun 1, 2020
Anticipated Primary Completion Date :
Sep 1, 2021
Anticipated Study Completion Date :
Dec 31, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: cybertherapy

use of cybertherapy (8 sessions) in addition to cognitive behavioral therapy (4 sessions) (pharmacological treatment are note modified)

Behavioral: Virtual Reality-Enhanced Cognitive Behavioral Therapy (VR-CBT)
use of cybertherapy (8 sessions) in addition to cognitive behavioral therapy (4 sessions) (pharmacological treatment are note modified)

Behavioral: Treatment as usual
Treatment as usual is a cognitive behavioral therapy I (4 sessions) (pharmacological treatment are note modified)

Other: Treatment as usual

Treatment as usual is a cognitive behavioral therapy I (4 sessions) (pharmacological treatment are note modified)

Behavioral: Treatment as usual
Treatment as usual is a cognitive behavioral therapy I (4 sessions) (pharmacological treatment are note modified)

Outcome Measures

Primary Outcome Measures

  1. Percentage of relapser patients at 3 months post-intervention [day 90 after intervention]

    recovery in consumption of cocaine at M3 after intervention

Secondary Outcome Measures

  1. Craving score [day 30 after intervention]

    evaluation of craving score (/10) compared to inclusion score

  2. Craving score [day 90 after intervention]

    evaluation of craving score (/10) compared to inclusion score

  3. Score on the personal efficiency sentiment scale [day 30 after intervention]

    Evaluation of the score on the personal efficiency sentiment scale

  4. Score on the personal efficiency sentiment scale [day 90 after intervention]

    Evaluation of the score on the personal efficiency sentiment scale

  5. Consumption of quantity of cocaine [day 30 after intervention]

    Evaluation of quantity of cocaine consumed

  6. Consumption of quantity of cocaine [day 60 after intervention]

    Evaluation of quantity of cocaine consumed

  7. Consumption of quantity of cocaine [day 90 after intervention]

    Evaluation of quantity of cocaine consumed

  8. Frequency of consumption of cocaine [day 30 after intervention]

    Evaluation of the frequency of cocaine consumption

  9. Frequency of consumption of cocaine [day 60 after intervention]

    Evaluation of the frequency of cocaine consumption

  10. Frequency of consumption of cocaine [day 90 after intervention]

    Evaluation of the frequency of cocaine consumption

  11. Way of consumption of cocaine [day 30 after intervention]

    Evaluation of the way of cocaine consumption

  12. Way of consumption of cocaine [day 60 after intervention]

    Evaluation of the way of cocaine consumption

  13. Way of consumption of cocaine [day 90 after intervention]

    Evaluation of the way of cocaine consumption

  14. amount of cocaine consumed during relapse [day 30 after intervention]

    Evaluation of cocaine amount consumed during relapse

  15. amount of cocaine consumed during relapse [day 90 after intervention]

    Evaluation of cocaine amount consumed during relapse

  16. Frequence of cocaine consumed during relapse [day 30 after intervention]

    Evaluation of cocaine frequence consumption during relapse

  17. Frequence of cocaine consumed during relapse [day 90 after intervention]

    Evaluation of cocaine frequence consumption during relapse

  18. Percentage of relapser patients [day 30 after intervention]

    recovery in relapser patients at M1 after intervention

  19. Duration of abstinence [day 30 after intervention]

    recovery of abstinence duration

  20. Duration of abstinence [day 60 after intervention]

    recovery of abstinence duration

  21. Duration of abstinence [day 90 after intervention]

    recovery of abstinence duration

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • suffering from a cocaine use disorder with craving criteria present according to the criteria of DSM 5

  • wanting to stop cocaine use

  • able to give informed consent to participate in research

  • Covered by a Social Security plan.

Exclusion Criteria:
Patient with:
  • psychiatric comorbidities (DSM 5) unstabilized

  • dipsomaniac alcoholism

  • an anteriority of one or more hypomanic or manic episodes

  • unstabilized psychosis

  • an unstabilized depression

  • a severe suicidal risk

  • a syndrome of dependence on products other than cocaine or tobacco

  • unstabilized anxiety

  • problems that hinder participation in 3D exposure, as a tendency to dissociation; phobias of the type of information (panic attacks and hypochondria...) severe dizziness...

  • cognitive problems limiting or preventing the possibility of implementing coping or managing emotions or stimuli and disabilities to complete questionnaires

  • a language barrier

  • a serious intercurrent pathology

  • the need for weekly individual follow-up Patient in a protected population such as pregnant women, lactating women, patients under guardianship, guardianship, deprived of freedoms, or in safeguarding justice

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU Clermont Ferrand Clermont-Ferrand Auvergne France 63000

Sponsors and Collaborators

  • University Hospital, Clermont-Ferrand
  • Fondation de l'Avenir, France

Investigators

  • Principal Investigator: Georges Brousse, University Hospital, Clermont-Ferrand

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Clermont-Ferrand
ClinicalTrials.gov Identifier:
NCT04280900
Other Study ID Numbers:
  • RBHP 2019 BROUSSE
  • 2019-A02368-49
First Posted:
Feb 21, 2020
Last Update Posted:
Feb 21, 2020
Last Verified:
Feb 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital, Clermont-Ferrand
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 21, 2020