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L'essai clinique NCT05336188 pour Troubles liés aux opioïdes, Applications mobiles, Traitement de substitution aux opiacés, Imagerie par résonance magnétique, Envie, Attentional Bias, Ecological Momentary Assessment est en recrutement. Consultez la vue en carte du Radar des Essais Cliniques et les outils de découverte par IA pour tous les détails, ou posez vos questions ici.
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Neurocognitive Mechanisms Underlying Smartphone-Assisted Prevention of Relapse in Opioid Use Disorder

En recrutement
Les détails de l'essai clinique sont principalement disponibles en anglais. Cependant, l'IA Trial Radar peut vous aider ! Cliquez simplement sur 'Expliquer l'essai' pour voir et discuter des informations sur l'essai dans la langue sélectionnée.
L'essai clinique NCT05336188 est conçu pour étudier le treatment de Troubles liés aux opioïdes, Applications mobiles, Traitement de substitution aux opiacés, Imagerie par résonance magnétique, Envie, Attentional Bias, Ecological Momentary Assessment. Il s'agit d'un essai interventionnel en Phase II. Son statut actuel est : en recrutement. L'essai a débuté le 16 mai 2023 et vise à recruter 255 participants. Dirigé par l'Université de l'Arkansas, l'essai devrait être terminé d'ici le 30 septembre 2028. Les données du site ClinicalTrials.gov ont été mises à jour pour la dernière fois le 13 mai 2025.
Résumé succinct
The proposed clinical trial would evaluate the use of smartphone applications ("apps", which have well-established efficacy in reducing cigarette and alcohol use) to prevent relapse among patients receiving medication-assisted treatment for opioid use disorder. In addition to standard app-based self-monitoring of drug use and personalized feedback, project innovation is enhanced by the proposed use of location-tracking technology for targeted, personalized intervention when participants enter self-identified areas of high risk for relapse. Furthermore, the proposed sub-study would use longitudinal functional neuroimaging to elucidate the brain-cognition relationships underlying individual differences in treatment outcomes, offering broad significance for understanding and enhancing the efficacy of this and other app-based interventions.
Description détaillée
The rising public health burden of opioid misuse, coupled with high relapse rates among individuals seeking treatment for opioid use disorder, necessitates novel interventions for improving opioid-related treatment response. Mobile technology such as smartphone-based applications ("apps") represent one such intervention. Although smartphone apps are effective in reducing cigarette and alcohol use, their efficacy for reducing opioid use has not yet been established. The proposed clinical trial would evaluate the app OptiMAT ("Optimizing Medication-Assisted Treatment") to prevent relapse among patients receiving medication-assisted treatment for opioid use disorder. OptiMAT implements two features shown to be effective for reducing substance use: daily self-monitoring of opiate use coupled with personalized feedback. Aim 1 would accrue 255 participants with 1:1 randomization into two arms (OptiMAT vs. Monitoring only) to evaluate differences in monthly opioid use at six months post-enrollment. Aim 2 would enroll a subset of participants (N=120; 60 per arm) into a longitudinal functional neuroimaging (fMRI) study to model the neurocognitive mechanisms underlying individual differences in treatment response. Two putative mechanisms (attentional bias for drug cues and cue-induced craving) promoting abstinence would be studied. Aim 3 would explore the use of location-based geographic ecological momentary assessment (GEMA) for targeted intervention when participants enter self-identified areas of high risk for relapse. Collectively, the proposed aims would (1) evaluate mobile technology applications for reducing opiate use, (2) understand the neurocognitive mechanisms of action to improve upon this and other apps aiming to reduce drug use, and (3) evaluate the role of personalized, contextually-relevant intervention to promote successful treatment outcomes.
Titre officiel

Neurocognitive Mechanisms Underlying Smartphone-Assisted Prevention of Relapse in Opioid Use Disorder

Conditions
Troubles liés aux opioïdesApplications mobilesTraitement de substitution aux opiacésImagerie par résonance magnétiqueEnvieAttentional BiasEcological Momentary Assessment
Publications
Articles scientifiques et travaux de recherche publiés sur cet essai clinique:
Autres identifiants de l'essai
  • 274084
Numéro NCT
Date de début (réel)
2023-05-16
Dernière mise à jour publiée
2025-05-13
Date de fin (estimée)
2028-09-30
Inscription (estimée)
255
Type d'essai
Interventionnel
PHASE
Phase II
Statut
En recrutement
Objectif principal
Traitement
Plan d'attribution
Randomisé
Modèle d'intervention
Parallèle
Masquage
Triple aveugle
Bras / Interventions
Groupe de participants/BrasIntervention/Traitement
ExpérimentalSmartphone
Participants randomized into the Smartphone app arm would use the smartphone app OptiMAT in conjunction with treatment as usual (TAU). Participants would use OptiMAT to complete daily self-assessments of opiate misuse, opiate craving, opiate withdrawal, and mood. The app will personalized feedback for maintaining abstinence goals. The app would also use geographic ecological momentary assessment (GEMA) to intervene via push notification when participants enter areas previously identified as high-risk for opiate use.
Smartphone
Adjunctive Smartphone app for improving MAT outcomes
Aucune interventionMonitoring Only
Participants randomized into the Monitoring Only arm would undergo treatment as usual (TAU) but without the smartphone app.
N/A
Critère principal d'évaluation
Critères d'évaluationDescription de critèresPériode
Urinalysis - Week 0 (Intake)
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
1 day
Urinalysis - Week 1
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
1 week
Urinalysis - Week 2
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
2 weeks
Urinalysis - Week 3
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
3 weeks
Urinalysis - Week 4
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
4 weeks
Urinalysis - Week 5
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
5 weeks
Urinalysis - Week 6
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
6 weeks
Urinalysis - Week 7
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
7 weeks
Urinalysis - Week 8
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
8 weeks
Urinalysis - Week 9
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
9 weeks
Urinalysis - Week 10
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
10 weeks
Urinalysis - Week 11
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
11 weeks
Urinalysis - Week 12
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
12 weeks
Urinalysis - Week 13
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
13 weeks
Urinalysis - Week 14
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
14 weeks
Urinalysis - Week 15
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
15 weeks
Urinalysis - Week 16
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
16 weeks
Urinalysis - Week 17
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
17 weeks
Urinalysis - Week 18
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
18 weeks
Urinalysis - Week 19
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
19 weeks
Urinalysis - Week 20
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
20 weeks
Urinalysis - Week 21
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
21 weeks
Urinalysis - Week 22
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
22 weeks
Urinalysis - Week 23
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
23 weeks
Urinalysis - Week 24
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
24 weeks
Urinalysis - Week 25
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
25 weeks
Urinalysis - Week 26
Percent of weekly urinalysis tests positive for opioid metabolite other than Suboxone
26 weeks
Critère secondaire d'évaluation
Critères d'évaluationDescription de critèresPériode
TLFB - Month 0 (Intake)
Days per Month of self-reported opioid misuse from monthly TimeLine FollowBack calendar over past 30 days
1 day
TLFB - Month 1
Days per Month of self-reported opioid misuse from monthly TimeLine FollowBack calendar over past 30 days
1 month
TLFB - Month 2
Days per Month of self-reported opioid misuse from monthly TimeLine FollowBack calendar over past 30 days
2 months
TLFB - Month 3
Days per Month of self-reported opioid misuse from monthly TimeLine FollowBack calendar over past 30 days
3 months
TLFB - Month 4
Days per Month of self-reported opioid misuse from monthly TimeLine FollowBack calendar over past 30 days
4 months
TLFB - Month 5
Days per Month of self-reported opioid misuse from monthly TimeLine FollowBack calendar over past 30 days
5 months
TLFB - Month 6
Days per Month of self-reported opioid misuse from monthly TimeLine FollowBack calendar over past 30 days
6 months
Treatment Continuation - Week 1
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
1 week
Treatment Continuation - Week 2
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
2 weeks
Treatment Continuation - Week 3
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
3 weeks
Treatment Continuation - Week 4
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
4 weeks
Treatment Continuation - Week 5
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
5 weeks
Treatment Continuation - Week 6
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
6 weeks
Treatment Continuation - Week 7
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
7 weeks
Treatment Continuation - Week 8
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
8 weeks
Treatment Continuation - Week 9
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
9 weeks
Treatment Continuation - Week 10
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
10 weeks
Treatment Continuation - Week 11
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
11 weeks
Treatment Continuation - Week 12
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
12 weeks
Treatment Continuation - Week 13
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
13 weeks
Treatment Continuation - Week 14
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
14 weeks
Treatment Continuation - Week 15
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
15 weeks
Treatment Continuation - Week 16
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
16 weeks
Treatment Continuation - Week 17
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
17 weeks
Treatment Continuation - Week 18
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
18 weeks
Treatment Continuation - Week 19
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
19 weeks
Treatment Continuation - Week 20
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
20 weeks
Treatment Continuation - Week 21
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
21 weeks
Treatment Continuation - Week 22
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
22 weeks
Treatment Continuation - Week 23
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
23 weeks
Treatment Continuation - Week 24
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
24 weeks
Treatment Continuation - Week 25
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
25 weeks
Treatment Continuation - Week 26
Binary variable if participant is still in treatment (yes/no). Survival analysis will determine if duration of treatment (i.e. time to treatment discontinuation) differs between study arms
26 weeks
Critères d'éligibilité

Âges éligibles
Adulte, Adulte âgé
Âge minimum
18 Years
Sexes éligibles
Tous
  • Sex: male or female
  • Age: 18 years and older
  • (MRI sub-study): Age: 18-50 years old
  • In Phase I treatment of MAT for opioid-use disorder. (Phase I indicates that patient is receiving no more than one week of take-home medications at each weekly clinic visit.)
  • Must be willing to use a smartphone if randomized to the smartphone intervention arm
  • (MRI sub-study): Native English-speaking

  • (MRI) Medical history: A history of neurological, cardiovascular, or infectious disease would exclude study participation. A loss of consciousness of 20 or more min or other evidence of brain trauma also would be exclusionary.
  • (MRI) Pregnancy: A positive test for pregnancy prior to fMRI would exclude participation, due to unknown effect of high-field MRI on developing fetus.
  • (MRI) MRI contraindications: Exclusion criteria for MRI include (1) the presence of non-removable internal (e.g., cardiac pacemakers, aneurysm clips, artificial joints) or external (e.g., piercings, orthodontics) ferromagnetic objects; (2) claustrophobia in a confined MRI environment; (3) medications that interfere with hemodynamic coupling (e.g., beta blockers); (4) hypersensitivity to loud noise; or (5) a body circumference exceeding 60cm due to broad shoulders or morbid obesity
Contact central de l'essai
Contact: Andrew James, Ph.D., 501-526-8345, [email protected]
1 Centres de l'essai dans 1 pays

Arkansas

Brain Imaging Research Center, Little Rock, Arkansas, 72227, United States
Deborah Hodges, MS, Contact, 5014202653, [email protected]
Natalie Morris, BS, Contact, 5014202653, [email protected]
George James, PhD, Investigateur principal
En recrutement