Understanding Pathways to Wellness and Recovery in Detroit - Digital Recovery Support Services (UPWARD D-RSS)
20. juli 2026 opdateret af: Sharon Reif, Brandeis University
UPWARD Study RCT of Digital Recovery Support Services (D-RSS) Among a Black Population in Recovery From Alcohol Use Disorders
The goal of this clinical trial is to learn if digital recovery support services (such as smartphone app) help to support alcohol recovery. We focus on a community of Black and African American people with alcohol use disorder (AUD) who receive in-person recovery support services from a recovery community center.
Participants will:
- Have an initial 2-hour in-person visit with the research team. During this visit, participants will be asked about themselves and their recovery from alcohol problems. They will also learn about digital recovery resources.
- Use digital recovery resources on their own for 12 weeks.
- Complete a short, weekly survey about their experience using digital recovery resources.
- Have a follow-up 1-hour in-person visit where the researcher asks about again about the participants, their recovery and how they felt about using the digital recovery support services.
Studieoversigt
Status
Rekruttering
Intervention / Behandling
Detaljeret beskrivelse
See study Detailed Protocol in Study Documents.
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
65
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Audrey Hildebrandt
- Telefonnummer: 781-736-8657
- E-mail: ahildebrandt@brandeis.edu
Studiesteder
-
-
Michigan
-
Detroit, Michigan, Forenede Stater, 48208
- Rekruttering
- Detroit Recovery Project
-
Kontakt:
- Research Manager
- Telefonnummer: 355 313-365-3100
- E-mail: upwardproject@brandeis.edu
-
Kontakt:
- Senior Project Manager
- Telefonnummer: 781-736-8657
- E-mail: ahildebrandt@brandeis.edu
-
Ledende efterforsker:
- Sharon Reif, PhD
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ingen
Beskrivelse
Inclusion Criteria:
- Able to communicate in English and read at an 8th grade reading level.
- Able to read and sign an informed consent form.
- Comfortable with smartphone technology or willing and able to learn.
- Identify as Black or African American.
- Is an adult over the age of 18.
- Is in recovery from alcohol problems for at least 3 months and no more than 5 years.
- Is receiving in-person recovery support services at our partner recovery community center at the time of screening and enrollment.
- Willing to receive and respond to weekly texts with a survey link for brief assessments, and complete two in-person research assessments (baseline and 13-week).
Exclusion Criteria:
Does not meet inclusion criteria
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Sundhedstjenesteforskning
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: TAU + DRSS
At the initial in-person visit, participants will complete a structured interview of baseline assessments and will be provided with a menu of digital recovery support services (D-RSS) to participants, technical assistance, and a phone and data plan (if needed).
The research team will discuss the D-RSS menu with the participants and guide them through app installation and use.
Following the initial visit, it is up to the participants to engage with the D-RSS.
We will send a text survey 1 week after the visit, and each week thereafter for 12 weeks, that assesses their engagement with in-person recovery supports, D-RSS, and their current recovery status.
The 3-month visit will be scheduled in the week following the last (week 12) text survey, at which participants will meet with research staff for a final in-person assessment.
|
The primary intervention is the provision of a menu of digital recovery support services (D-RSS) to participants, along with a phone and data plan (if needed) and technical assistance.
We have created a menu of D-RSS options that have been vetted by our team as appropriate for a range of recovery goals (e.g., manage emotions, track sobriety, connect with others) and for a range of technological literacy, as well as being culturally relevant or at minimum culturally agnostic.
Types of D-RSS presented to participants include mobile applications, websites, and video playlists, all of which relate to and support addiction recovery.
Participants also may use other D-RSS that they identify.
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Usability and Acceptability of D-RSS
Tidsramme: At the end of the trial (13 weeks)
|
We include a module consisting of 20 items measuring usability and acceptability on a 4-point Likert scale (strongly disagree, disagree, agree, strongly agree).
These items were selected from several sources, so do not have a pre-existing scale; we will consider whether a scale is appropriate by examining inter-item correlations and Cronbach's alphas for potentially conceptually similar subsets of items.
|
At the end of the trial (13 weeks)
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Sharon Reif, PhD, Brandeis University
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
13. juni 2026
Primær færdiggørelse (Anslået)
1. december 2026
Studieafslutning (Anslået)
1. maj 2027
Datoer for studieregistrering
Først indsendt
20. juli 2026
Først indsendt, der opfyldte QC-kriterier
20. juli 2026
Først opslået (Faktiske)
24. juli 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
24. juli 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
20. juli 2026
Sidst verificeret
1. juli 2026
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 22126R
- R01AA029817 (U.S. NIH-bevilling/kontrakt)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
JA
IPD-planbeskrivelse
All data from the trial will be shared via the NIAAA data archive.
IPD-delingstidsramme
July 2026 to July 2029
IPD-delingsadgangskriterier
Deidentified subject data will be available to those who meet the expectations of the NIAAA data archive.
Supporting data will be available through clinicaltrials.gov
or upon request.
IPD-deling Understøttende informationstype
- STUDY_PROTOCOL
- SAP
- ICF
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
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