ClinicalTrials.Veeva

Menu

The Longitudinal Impact of SES and the CNDS on Recovery From SUD

Virginia Polytechnic Institute and State University logo

Virginia Polytechnic Institute and State University

Status

Not yet enrolling

Conditions

Substance Use Disorders

Treatments

Other: Online Survey

Study type

Observational

Funder types

Other

Identifiers

NCT05103514
SES- Longitudinal Study

Details and patient eligibility

About

The goal of this study is to provide a scientific understanding of the impact of socioeconomic status (SES) on the recovery trajectory (psychosocial functioning, relapse/remission status, and neurocognitive mechanisms).

Full description

The study will characterize the effect of SES (subjective and objective indicators) on long-term trajectories of recovery and neurocognitive functioning. By using an accelerated longitudinal design, the investigators will examine the association between baseline SES, changes in CNDS, and changes in psychosocial functioning (e.g., quality of life) and relapse. Moreover, the investigators will use computational modeling to capture underlying changes in components of CNDS functioning related to SES and SUD recovery.

Enrollment

675 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. be ≥18 yrs old
  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

  1. Minors will not be included
  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

Trial design

675 participants in 3 patient groups

Cohort 1
Description:
Participants in this group started their recovery process \< 1 year ago
Treatment:
Other: Online Survey
Cohort 2
Description:
Participants in this group started their recovery process 1 to \<2 years ago
Treatment:
Other: Online Survey
Cohort 3
Description:
Participants in this group started their recovery process 2 to \<3 years ago
Treatment:
Other: Online Survey

Trial contacts and locations

0

Loading...

Central trial contact

Kirstin M Gatchalian; Warren K Bickel, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems