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Cognitive Functioning in Opioid Use Disorder

N

New York State Psychiatric Institute

Status

Terminated

Conditions

Opioid-use Disorder
Cognitive Change
Opioid Use

Treatments

Other: CogMed

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This outpatient study is designed to examine the potential relationship between non-fatal opioid overdose and cognitive functioning. This study will also examine the impact of computerized working memory training on relevant outcomes (cognition, psychosocial functioning, quality of life, drug use). The training component of the study lasts 1 month, with follow up visits and 1-month and 3-months post training.

Full description

This outpatient study is designed to examine the potential relationship between non-fatal opioid overdose (i.e. overdose that does not result in death), cognitive functioning, and the impact of computerized working memory training on relevant outcomes (cognition, psychosocial functioning, quality of life). Participants (n=30) with a history of at least one prior opioid OD, who are enrolled in buprenorphine treatment, will be randomized to 20 sessions of an active (n=15) or sham (n=15) working memory training. Patients will complete measures of cognitive functioning during screening, post-training, and at 1-month and 3-month follow up. Participants will also complete the measures of decision making, psychosocial functioning and drug use at baseline, post-training, and follow up.

Enrollment

13 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Meets DSM-5 criteria for moderate-severe Opioid Use Disorder (OUD) in the past 6 months
  • Enrolled in a suboxone (buprenorphine/naloxone) program; willing to provide consent for research team to contact treatment provider
  • History of at least 1 prior opioid overdose
  • Recent history of illicit opioid use
  • In good physical health
  • Access to a smartphone, tablet, or computer

Exclusion criteria

  • Evidence of a co-occurring, untreated psychiatric condition that would make participation risky or difficulty
  • Lack of access to a home computer, smartphone, or tablet
  • Unable to speak, read and/or communicate in English

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

13 participants in 2 patient groups

Active
Experimental group
Description:
Working memory training with task-difficulty increasing across sessions
Treatment:
Other: CogMed
Sham
Active Comparator group
Description:
Working memory training with task-difficulty remaining constant across sessions.
Treatment:
Other: CogMed

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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