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

November 8, 2016 updated by: National Health Research Institutes, Taiwan

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.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

340

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Miaoli County, Taiwan, 35053
        • National Health Research Institute
    • ChangHua
      • Lukang, ChangHua, Taiwan, 50550
        • Changhua Christian Hospital
    • New Taipei
      • Banqiao, New Taipei, Taiwan, 22060
        • Far Eastern Memorial Hospital
      • Sanxia, New Taipei, Taiwan, 23702
        • En-Chu-Gong Hospital
    • New Taipei City
      • Banqiao, New Taipei City, Taiwan, 22060
        • Far Eastern Memorial Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

  1. Normal control group:

    Healthy adults will be recruited from community.

  2. Methadone Maintenance treatment group Study subjects will be enrolled only in the methadone clinic.
  3. Buprenorphine/Naloxone treatment group Subjects will be enrolled only in the clinic.
  4. Drug-free ex-addict group Subjects will be recruited from the therapeutic communities and halfway house of Operation Dawn.

Description

  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

    Exclusion criteria:

    1. Patients with comorbid severe mental disorders including:

      1. Organic mental disorders, or
      2. Schizophrenia
    2. Severe cognitive impairment
    3. Being pregnant
  3. Buprenorphine/Naloxone treatment group (BNT)

    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 buprenorphine maintenance therapy for at least 3 months
    6. No change of buprenorphine dosage for the last week
    7. Regularly took buprenorphine for the last week
    8. 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. Severe cognitive impairment
    3. Being pregnant
  4. Medication-free ex-addict group (MF)

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. Diagnosis of Heroin dependence by DSM-IV definition
  5. 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. Severe cognitive impairment
  3. Being pregnant
  4. Exposure of methadone, buprenorphine and other opioid treatment in the previous 3 months

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Methadone maintenance treatment (MMT)
Buprenorphine-Naloxone treatment (BNT)
Medication-free ex-addicts(MF)
Normal control (NC)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Group differences in demopraphics
Time Frame: one year
support system, vital sign, substance use history
one year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Gruop differences in neuro-cognitive functions
Time Frame: one year
attention, executive function, decision making
one year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Sheng-Chang Wang, M.D., M.Sc., National Health Research Institutes, Taiwan

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

March 1, 2009

Primary Completion (Actual)

December 1, 2013

Study Completion (Actual)

December 1, 2013

Study Registration Dates

First Submitted

August 16, 2012

First Submitted That Met QC Criteria

August 16, 2012

First Posted (Estimate)

August 20, 2012

Study Record Updates

Last Update Posted (Estimate)

November 9, 2016

Last Update Submitted That Met QC Criteria

November 8, 2016

Last Verified

August 1, 2012

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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