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Enhancing Prospective Thinking in Early Recovery (HOME)

Enhancing Prospective Thinking in Early Recovery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06302413
Acronym
HOME
Enrollment
500
Registered
2024-03-08
Start date
2024-02-15
Completion date
2027-07-31
Last updated
2026-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alcohol Use Disorder

Brief summary

The goal of this clinical trial is to use a novel virtual reality intervention to test for efficacy in reducing alcohol use and increasing abstinence, with concomitant increases in future self-identification, future time perspective, and delay-of-reward, in early recovering alcohol use disorder (AUD) persons. The main question\[s\] this trial aims to answer are: Will the Virtual Reality (VR) intervention decrease the number of stimulant use days? Will the VR intervention produce longer abstinence periods during follow-up visits? Will the VR intervention increase alcohol abstinence rates? Will the VR intervention increase future self-identification? Will the VR intervention increase self-reported future time perspective? Will the VR intervention increase preference for delayed rewards in a laboratory delay discounting task on the study day? Will the VR intervention produce gains in the behavioral effects of future self-identification, future time perspective, and delayed rewards at the 30-day and 6-month follow-ups? Researchers will compare the experimental and control groups to see if there are differences in the results for the questions outlined above.

Interventions

DEVICEVirtual Reality

They will receive a Virtual Reality Park experience, which is an empty park with no avatars. They will then have a Virtual Reality Avatar experience, where they will see an avatar resembling themselves in a park setting.

Sponsors

Indiana University
Lead SponsorOTHER
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Masking description

All study participants are randomly assigned to a group prior to study enrollment. Participants will not be made aware of their group assignment.

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Abstinence between ≥14 days and ≤1 year * Verbal endorsement of commitment to recovery * Outpatient * Psychotropic drugs for SUD-comorbidity * Drug/alcohol abstinence ≥ 24 hours at the time of the study day visit * English comprehension

Exclusion criteria

* Unstable medical disorders * Habitual drug use * Mu-opioid drugs * Smell/taste disorders * Unstable psychiatric conditions * Extravagant/elaborate face tattoos

Design outcomes

Primary

MeasureTime frameDescription
Reduced Use of Drug Using DaysDay 2-Study Day Visit; 30-day Follow-up Visit; 6-month Follow-up VisitThe Virtual Reality Avatar experience will reduce drug using days.
Increased Length of AbstinenceDay 2-Study Day Visit; 30-day Follow-up Visit; 6-month Follow-up Visit.The Virtual Reality Avatar experience will increase the length of abstinence periods.
Increased (overall) AbstinenceDay 2-Study Day Visit; 30-day Follow-up Visit; 6-month Follow-up Visit.The Virtual Reality Avatar experience will increase abstinence.
Future Self-identification with Future Self Continuity QuestionnaireDay 2-Study Day Visit; 30-day Follow-up Visit; 6-month Follow-up VisitThe Virtual Reality Avatar experience will increase future self-identification.
Future Time Perspective with the Delayed Discounting Behavioral Task and Future Self Continuity QuestionnaireDay 2-Study Day Visit; 30-day Follow-up Visit; 6-month Follow-up Visit.The Virtual Reality Avatar experience will increase future time perspective.
Delayed Reward Preference with the Delayed Discounting Behavioral TaskDay 2-Study Day Visit; 30-day Follow-up Visit; 6-month Follow-up Visit.The Virtual Reality Avatar experience will increase preference for delayed rewards.

Countries

United States

Contacts

CONTACTSarah Turo, BA
sturo@iu.edu317-963-7220
CONTACTColton Lind, BS
cmlind@iu.edu317-963-2554
PRINCIPAL_INVESTIGATORBrandon G Oberlin, PhD

Indiana University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 5, 2026