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Predicting Dropout and Outcome From Neuropsychological Functions in SUD Patients

University of Oslo (UIO) logo

University of Oslo (UIO)

Status

Active, not recruiting

Conditions

Substance Use Disorder (SUD)

Study type

Observational

Funder types

Other

Identifiers

NCT03220373
2015/11288

Details and patient eligibility

About

The aim of this project is to gain a more specific understanding of how different cognitive profiles predict residential treatment drop-out, treatment retention and post-treatment outcome in a population with Substance Use Disorder.

Full description

This project collects the neuropsychological profile of residential SUD patients, in addition to treatment length, exit reason, hospital journal data and post-treatment clinical outcome data. The project aims to identify clinically relevant neurocognitive domains that predict treatment dropout and post-treatment clinical outcome. This will make it possible for future clinicians to focus their effort on neurocognitive functions most relevant for this particular patient group.

RESEARCH QUESTIONS:

  1. What neurocognitive domain (and sub-domain) are the strongest predictor of treatment drop-out and retention?
  2. What neurocognitive domain (and sub-domain) are the strongest predictor of post-treatment clinical outcome variables such as drug use, health and social integration.
  3. Will data on treatment length, age, gender, substance abuse history or psychiatric co-morbidity predict outcome independently, or in interaction with, the neuropsychological profile?

This longitudinal prospective cohort study aims for a continuous collection of neuropsychological data baseline and post-treatment follow-up data until 2030.

Enrollment

200 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Substance Use Disorder (SUD) patients.
  • 18 years or older.
  • Qualified to consent to research participation.
  • Able to speak and write in Norwegian.

Exclusion criteria

  • Not qualified to consent to research participation.
  • Insufficient understanding of Norwegian.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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