- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04650386
Undersøgelse af en adaptiv tilgang til at yde psykosocial støtte til buprenorphinpatienter
Forbedring af kontorbaseret buprenorphinbehandling: en adaptiv psykosocial tilgang
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Denne undersøgelse vil hjælpe med at informere om bedste praksis for at give psykosocial behandling inden for rammerne af kontorbaseret opioidbehandling (OBOT) med buprenorphin. Vi vil bruge en trinvis tilgang til at udvikle og evaluere en adaptiv tilgang til levering af supplerende psykosocial behandling, der inkluderer medicinhåndtering af en buprenorphinudbyder og kobling til CRS og CBT afhængigt af patientens behov. De specifikke mål med forslaget er anført nedenfor.
Mål 1: Arbejd i samarbejde med vores tværfaglige team for at udvikle specifikke protokoller for CRS- og CBT-interventionerne og etablere algoritmer baseret på adfærdskriterier for at bestemme, hvornår hver intervention skal implementeres. Som en del af dette mål vil vi også udvikle standardprocedurer for levering af hver intervention og uddanne interventionister [dvs. CRS'er og Licensed Professional Counselors (LPC'er)] til at levere dem med troskab.
Formål 2: Udfør et randomiseret studie i to grupper for at evaluere effektiviteten af den adaptive intervention i forhold til TAU. Resultater, der skal undersøges, vil omfatte urinanalyse-bekræftet opioidbrug, retention i buprenorphin-baseret OBOT, livskvalitet og psykosocial funktion gennem et år post-studiet.
Mål 3: Foretag en kvalitativ evaluering af interventionen og udvikle en strategisk plan for formidlingen af den. Vi vil gennemføre fokusgrupper med klinikpersonale og relevante interessenter for at bestemme nytten og acceptablen af den adaptive intervention. Derudover vil vi afholde et ekspert-rundbordsbord for at identificere mekanismer til at øge bæredygtigheden og forbedre anvendelsen af andre kontorbaserede buprenorphinprogrammer for at informere udviklingen af den strategiske plan.
Mål 4: Etablere et træningsprogram i klinisk forskning for minoritetsstuderende. Otte bachelorstuderende fra en historisk minoritetsinstitution vil blive udvalgt til at deltage i 9-måneders praktikophold, hvor de vil modtage omfattende og pragmatisk træning i hele spektret af klinisk forskning fra studiedesign til formidling.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Pennsylvania
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Philadelphia, Pennsylvania, Forenede Stater, 19121
- Project HOME Stephen J. Klein Wellness Center
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Philadelphia, Pennsylvania, Forenede Stater, 19123
- PHMC Care Clinic
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Beskrivelse
Inklusionskriterier:
- Har påbegyndt kontorbaseret buprenorphinbehandling for OUD på FQHC inden for de sidste 4 uger;
- Kræver ikke et indlagt plejeniveau som bestemt af sundhedsudbyderen; og
- Være i stand til at give gyldige kontaktoplysninger og informeret samtykke.
Ekskluderingskriterier:
- Patienten er under 18 år;
- Komorbid psykiatrisk lidelse, der indikerer behov for mere intensiv behandling på boliger
- Patienten kan ikke give informeret samtykke.
Personer, der er berusede, kognitivt svækkede eller psykiatrisk ustabile ved baseline vil ikke blive inkluderet; de kan dog efterfølgende medtages, hvis diskvalificerende betingelse aftager.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Ingen indgriben: Behandling som sædvanlig (TAU)
Deltagere, der er tildelt TAU-tilstanden, vil blive planlagt til behandling af buprenorphinmedicin og vil modtage OBOT på FQHC og supplerende psykosocial behandling, som typisk ydes på FQHC.
Teamet vil fortsætte med at mødes med patienten under efterfølgende MAT-besøg med en faldende frekvens, med en lille stedspecifik variation.
Tidsplanen for MAT-besøg omfatter generelt 3 klinikbesøg i løbet af induktionsugen, 1-2 besøg om ugen, indtil patienten er stabiliseret, og derefter månedligt.
Adfærdssundhedsklinikere yder støtte til patienten, diskuterer UDS-resultater, hjælper med strategisk problemløsning omkring recovery og tilpasning til ædruelighed og overvåger patientens engagement i MAT.
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Eksperimentel: Adaptiv intervention
Deltagere, der er tildelt den adaptive interventionstilstand, vil blive planlagt til behandling af buprenorphinmedicin i henhold til klinikprotokollen beskrevet ovenfor for TAU.
Den supplerende psykosociale behandling, som deltagere i denne tilstand modtager, er (1) CBT leveret af adfærdssundhedsspecialister og/eller (2) peer-støtte leveret af certificeret recovery-specialist.
Den aktive interventionsperiode vil strække sig over 3 måneder efter studiestart.
Deltagerne vil fortsat modtage TAU efter den aktive interventionsperiode.
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Deltagere, der er tildelt den adaptive interventionstilstand, vil blive planlagt til behandling af buprenorphinmedicin i henhold til klinikprotokollen beskrevet ovenfor for TAU.
Den supplerende psykosociale behandling, som deltagere i denne tilstand modtager, er (1) CBT leveret af adfærdssundhedsspecialister og/eller (2) peer-støtte leveret af certificeret recovery-specialist.
Den aktive interventionsperiode vil strække sig over 3 måneder efter studiestart.
Deltagerne vil fortsat modtage TAU efter den aktive interventionsperiode.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Urinalyse-bekræftet afholdenhed fra opioider efter 3 måneders opfølgning
Tidsramme: 3 måneder efter studiestart
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Deltagerne vil give en urinprøve ved 3 måneders opfølgningsvurdering.
Vi vil bruge CLIA Waived® 14-Panel Drug Test Cup og fentanyl teststrimmel til opioider, buprenorphin, metadon, oxycodon, THC, kokain, amfetamin, PCP, metamfetamin, benzodiazepiner og barbiturater og MDMD.
Urinprøven vil blive leveret under opsyn af RA, som vil bruge standardprocedurer til at påvise manipulation og fortynding.
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3 måneder efter studiestart
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Urinalyse-bekræftet afholdenhed fra opioider efter 6 måneders opfølgning
Tidsramme: 6 måneder efter studieoptagelse
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Deltagerne vil give en urinprøve ved 6 måneders opfølgningsvurdering.
Vi vil bruge CLIA Waived® 14-Panel Drug Test Cup og fentanyl teststrimmel til opioider, buprenorphin, metadon, oxycodon, THC, kokain, amfetamin, PCP, metamfetamin, benzodiazepiner og barbiturater og MDMD.
Urinprøven vil blive leveret under opsyn af RA, som vil bruge standardprocedurer til at påvise manipulation og fortynding.
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6 måneder efter studieoptagelse
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Urinalyse-bekræftet afholdenhed fra opioider ved 9 måneders opfølgning
Tidsramme: 9 måneder efter studiestart
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Deltagerne vil give en urinprøve ved 9 måneders opfølgningsvurderingen.
Vi vil bruge CLIA Waived® 14-Panel Drug Test Cup og fentanyl teststrimmel til opioider, buprenorphin, metadon, oxycodon, THC, kokain, amfetamin, PCP, metamfetamin, benzodiazepiner og barbiturater og MDMD.
Urinprøven vil blive leveret under opsyn af RA, som vil bruge standardprocedurer til at påvise manipulation og fortynding.
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9 måneder efter studiestart
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Urinalyse-bekræftet afholdenhed fra opioider efter 12 måneders opfølgning
Tidsramme: 12 måneder efter studieoptagelse
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Deltagerne vil give en urinprøve ved 12 måneders opfølgningsvurderingen.
Vi vil bruge CLIA Waived® 14-Panel Drug Test Cup og fentanyl teststrimmel til opioider, buprenorphin, metadon, oxycodon, THC, kokain, amfetamin, PCP, metamfetamin, benzodiazepiner og barbiturater og MDMD.
Urinprøven vil blive leveret under opsyn af RA, som vil bruge standardprocedurer til at påvise manipulation og fortynding.
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12 måneder efter studieoptagelse
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Afholdenhed fra eller reduktion i brugen af andre (ikke-opioide) psykoaktive stoffer
Tidsramme: Gennem 12 måneder efter studieoptagelse
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Resultater fra CLIAwaived® 14-paneltesten og fentanylstrimlen beskrevet ovenfor for det primære resultat vil blive brugt som en indikator for dette resultat.
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Gennem 12 måneder efter studieoptagelse
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Retention i buprenorphin-baseret OBOT
Tidsramme: Gennem 12 måneder efter studieoptagelse
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Herunder mødemøde, medicin- og behandlingsoverholdelse samt fastholdelse i og afslutning af behandling.
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Gennem 12 måneder efter studieoptagelse
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Vurdering af livskvalitet
Tidsramme: Gennem 12 måneder efter studieoptagelse
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Livskvalitet vil blive målt ved hjælp af Short Form-36 (SF-36).
SF-36 er en selvrapporterende opgørelse, der vurderer otte dimensioner af fysisk og mental sundhedsrelateret livskvalitet.
SF-36 har vist sig at have høj reliabilitet og validitet.
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Gennem 12 måneder efter studieoptagelse
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Psykosocial funktionsevne/Multidimensional problemers sværhedsgrad
Tidsramme: Gennem 12 måneder efter studieoptagelse
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Flerdimensionel problemalvorlighed, et sekundært resultat, vil blive målt ved hjælp af Addiction Severity Index-Lite (ASI-Lite).
ASI-Lite er en pålidelig og gyldig multidimensionel vurdering, der giver sammensatte resultater, der afspejler det aktuelle problems sværhedsgrad inden for det medicinske, beskæftigelsesmæssige, alkohol-, narkotika-, juridiske, familie/sociale og psykiatriske område.
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Gennem 12 måneder efter studieoptagelse
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Behandlingstilfredshed
Tidsramme: Gennem 12 måneder efter studieoptagelse
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Behandlingstilfredsheden vil blive målt ved hjælp af en ændret version af Treatment Services Review (TSR).
TSR måler patientens terapeutiske engagement i og tilfredshed med behandlingen.
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Gennem 12 måneder efter studieoptagelse
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Samarbejdspartnere og efterforskere
Efterforskere
- Ledende efterforsker: Karen Dugosh, Ph.D., PHMC
Publikationer og nyttige links
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