The Longitudinal Impact of SES and the CNDS on Recovery From SUD
NCT ID: NCT05103514
Last Updated: 2025-07-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
675 participants
OBSERVATIONAL
2025-12-01
2028-07-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Substance Use Treatment and Its Role in Supporting Social Cognition
NCT06535919
Examining Effects of Domain Specific Episodic Future Thinking on Cannabis Use
NCT05324813
Barriers to Substance Use Disorder Recovery
NCT04098614
Computerized Screening, Brief Intervention, and Referral to Treatment in Primary Care
NCT01003834
Machine Learning Technology in Predicting Relapse and Implementing Peer Recovery Intervention Before Drug Use Occurs
NCT05976672
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Cohort 1
Participants in this group started their recovery process \< 1 year ago
Online Survey
There are no interventions planned for this study. This is an observational study only.
Cohort 2
Participants in this group started their recovery process 1 to \<2 years ago
Online Survey
There are no interventions planned for this study. This is an observational study only.
Cohort 3
Participants in this group started their recovery process 2 to \<3 years ago
Online Survey
There are no interventions planned for this study. This is an observational study only.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Online Survey
There are no interventions planned for this study. This is an observational study only.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. meet lifetime DSM-5 SUD criteria
3. have a Recovery Initiation Date less than 3 years prior to the time of enrollment
4. be able to read independently
5. be free of legal problems that could limit participation
6. reside in the U.S.
7. anticipate continued Internet access (to ensure ongoing contact and data collection)
8. be a registrant of the International Quit and Recovery Registry (IQRR)
Exclusion Criteria
2. Prisoners will not be included. If participants become incarcerated during this study, they will not be contacted to complete assessments during their incarceration. If the incarceration ends during the study, they may be contacted to participate in assessments.
3. Adults who are not capable of consenting on their own behalf
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Virginia Polytechnic Institute and State University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Jeffrey Stein
Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Warren Bickel, PhD
Role: PRINCIPAL_INVESTIGATOR
Virginia Polytechnic Institute and State University
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
SES- Longitudinal Study
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.