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Pharmacogenomics Study of Sleep Disturbance and Neurocognitive Impairments in the Opioid Addicts

Pharmacogenomics Study of Sleep Disturbance and Neurocognitive Impairments in the Opioid Addicts

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01668706
Enrollment
340
Registered
2012-08-20
Start date
2009-03-31
Completion date
2013-12-31
Last updated
2016-11-09

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

Conditions

Heroin Dependence

Brief summary

Opioid abuse is a complex problem, which not only impacts on addicts' physical and psychological health individually, but also threats the society. Recently, spread of HIV via sexual behavior and needle sharing among injecting drug users (IDUs) also becomes a serious public health problem all over the world. In Taiwan, since the first HIV-infected IDU identified in 1987, the incident cases have mounted to 2,461 in 2005. To prevent the epidemics of HIV among IDUs, the Center for Disease Control (CDC) thus collaborated with Department of Justice and implemented harm reduction programs in 2005. It is the milestone that opioid addiction is officially treated as a health rather than a legal issue in Taiwan. Among the harm reduction programs of needle and syringe exchange for IDUs as well as substitution treatment for opioid dependence, methadone maintenance treatment (MMT) is one of the most important parts. Till 2008, there were over 13,000 heroin addicts participated in more than 80 MMT programs. Although the clinical evidences have proven the superior effectiveness of maintenance therapy in ameliorating illicit substances abuse, decreasing criminality and improving quality of life, there are common problems of sleep disturbance and neurocognitive impairments among the subjects receiving opioid medications. The concerns of the adverse effects might thus frustrate the subjects' motivation and compliance to maintain treatments. However, sleep disturbance and neurocognitive impairments related to opioid medications are often neglected in the clinical practices and there are scanty researches focusing on these crucial issues in the existing literature. In this prospective study, four groups of subjects including methadone maintenance treatment, buprenorphine/naloxone, medication-free opioid ex-addicts and healthy volunteers will be enrolled. Via the comprehensive assessments including clinical interview, neurocognitive examinations, electrocardiogram-based sleep breathing detector and pharmacogenomical evaluation, we will not only have the opportunities to have more insights on the impacts of opioid medications on sleep and neurocognitive performances, but also develop more adequate strategies to improve motivation and outcome in treating the opioid addicts.

Interventions

None listed

Sponsors

National Health Research Institutes, Taiwan
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

1. Normal control group (NC): Inclusion criteria: 1. Chinese ethnicity 2. Men or women above age of 20 3. Able to participate in a clinical assessment in Chinese (including Mandarin and Taiwanese dialects) 4. Individuals who have completed a written consent form

Exclusion criteria

1. Patients with comorbid severe mental disorders including: 1. Organic mental disorders, or 2. Schizophrenia 2. Past diagnosis of Heroin dependence by DSM-IV definition 3. Severe cognitive impairment 4. Being pregnant 2. Methadone maintenance treatment group (MMT) Inclusion criteria: 1. Chinese ethnicity 2. Men or women above age of 20, below age of 65 3. Able to participate in a clinical assessment in Chinese (including Mandarin and Taiwanese dialects) 4. Diagnosis of Heroin dependence by DSM-IV definition 5. Enter methadone maintenance therapy for at least 3 months 6. No change of methadone dosage for the last week 7. Regularly took methadone for the last week 8. Individuals who have completed a written consent form

Design outcomes

Primary

MeasureTime frameDescription
Group differences in demopraphicsone yearsupport system, vital sign, substance use history

Secondary

MeasureTime frameDescription
Gruop differences in neuro-cognitive functionsone yearattention, executive function, decision making

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026