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The Pharmacogenetic Study , Readiness to Change, and Pharmacological Intervention for Smoking Cessation in Schizophrenia (PSIAARP)

Primary Purpose

Tobacco Dependence, Schizophrenia

Status
Completed
Phase
Phase 4
Locations
Taiwan
Study Type
Interventional
Intervention
Hihg-doseNRT, Low-dose NRT, bupropion
Sponsored by
Yu-Li Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tobacco Dependence focused on measuring Schizophrenia, NRT, Bupropion, Stages of change

Eligibility Criteria

16 Years - 65 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Competent volunteers completing consent form
  • Schizophreniform, schizoaffective,or psychotic disorder NOS based on DSMIV

Exclusion Criteria:

  • Severe life-threatening physical condition
  • Pregnancy
  • Fluroxamine treatment in the past 2 weeks
  • Allergy to nicotine or caffeine

Sites / Locations

  • Yuli hospital, DOH

Arms of the Study

Arm 1

Arm Type

Active Comparator

Arm Label

High-dose NRT, Low-dose NRT, bupropion

Arm Description

Outcomes

Primary Outcome Measures

7 day point prevalence of abstinence

Secondary Outcome Measures

smoking reduction more than 50% and 25%

Full Information

First Posted
June 30, 2007
Last Updated
April 13, 2010
Sponsor
Yu-Li Hospital
Collaborators
National Health Research Institutes, Taiwan, Department of Health, Executive Yuan, R.O.C. (Taiwan)
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1. Study Identification

Unique Protocol Identification Number
NCT00495352
Brief Title
The Pharmacogenetic Study , Readiness to Change, and Pharmacological Intervention for Smoking Cessation in Schizophrenia
Acronym
PSIAARP
Official Title
1. The Pharmacogenetic Study of Interaction Among Antipsychotics, Readiness to Change, and Pharmacological Intervention for Smoking Cessation Among Schizophrenic Patients 2. Stages of Change and Outcomes of Nicotine Replacement Therapy in Chronic Schizophrenic Patients
Study Type
Interventional

2. Study Status

Record Verification Date
April 2010
Overall Recruitment Status
Completed
Study Start Date
January 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
December 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Yu-Li Hospital
Collaborators
National Health Research Institutes, Taiwan, Department of Health, Executive Yuan, R.O.C. (Taiwan)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Cigarette smoking represents a major health problem for patients suffering from schizophrenia. Compared to the general population, schizophrenic patients are significantly more likely to be addicted to nicotine. They also are more likely to be heavy smokers, and tend to be exposed disproportionately to nicotine and other harmful ingredients in the cigarette because of the observed tendency to smoke down to the very end. Further, smoking in these patients may be associated with a higher risk for developing tardive dyskinesia All of these factors render schizophrenic patients a particularly vulnerable group for the detrimental effects of tobacco-related medical problems. Currently, there is little information available regarding the efficacy and utility of smoking cessation treatment methods, as well as factors that may predict patients' response to such treatments. An important related issue is the influence of smoking, and its cessation, on the effects of the medications most of these patients rely upon for the control of their psychiatric symptoms. Although smoking has long been known to significantly alter the metabolism, and thus the effects, of most antipsychotics, the extent and clinical significance of these influences have rarely been assessed. It is unclear to what extent smoke cessation (as well as initiation) changes the side effect profiles of these medications, and whether such changes contribute towards the difficulties in patients' ability and/or willingness to stop smoking. In addition, except pharmacological intervention, readiness to change may be an important factor affecting the outcomes of smoking reduction. Prochaska et al proposed the concept of stages of change to predict the response of quitting behavior for substance use. A lot of evidence support the stronger of readiness of change, the higher successful rate of quitting can be reached. Yet these results are largely found in many non-pharmacological intervention and smoking cessation programs for general population. Till now, no available study solely focus readiness of change quitting smoking behavior in NRT treatment for chronic schizophrenic patients. Thus, we have an a great interest in examining the association between the stages of change and the outcomes of smoking-cessation along with reduction among schizophrenic patients receiving transdermal nicotine patches. In order to begin addressing these important issues, this application proposes to utilize state-of-the-art methodologies derived from the field of pharmacogenetics, molecular biology and clinical trials, to (1) examine short-term and long-term efficacy of standard treatment methods, such as the use of nicotine patches, in this population; (2) identify factors that might predict treatment responses; and, (3) examine the interactions between smoking and the effect of antipsychotics, as well as how such interactions might affect smoking cessation. (4) to examine the predictive value of the stages of change on smoking cessation and reduction outcomes in schizophrenic patients receiving different doses of nicotine replacement therapy (NRT) and bupropion as implemented in a randomized trial.
Detailed Description
Specific Aims Accordingly, this proposal aims at testing the following major hypotheses: 1. Nicotine patch therapy and bupropion are effective in smoke cessation among motivated psychiatric outpatients with schizophrenia. 1a. High dose nicotine patch therapy is significantly more effective in inducing smoke cessation than regular dose nicotine patch therapy. 1b. Nicotine patch therapy and bupropion are more effective in inducing smoke cessation in those treated with "atypical" neuroleptics as compared to those treated with "typical" neuroleptics. 2. Response to nicotine patch therapy is associated with genetic polymorphisms of DRD2, dopamine transporter (DAT; SLC6A3), CYP2A6 and CYP2D6 genes. 3. Smoke cessation is associated with a significant decrease in the activity of CYP1A2, as well as a significant increase in the steady-state concentration of the neuroleptics received by the patients. This will lead to an increased incidence of treatment emergent side effects, which may be controlled by neuroleptic dose adjustment. 4. patients in the stage of preparation or contemplation (stronger readiness to quit smoking) are more likely to reduce smoking and stop smoking than those in the stage of precontemplation (weaker readiness to quitting smoking).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tobacco Dependence, Schizophrenia
Keywords
Schizophrenia, NRT, Bupropion, Stages of change

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
360 (Actual)

8. Arms, Groups, and Interventions

Arm Title
High-dose NRT, Low-dose NRT, bupropion
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Hihg-doseNRT, Low-dose NRT, bupropion
Primary Outcome Measure Information:
Title
7 day point prevalence of abstinence
Time Frame
8 weeks after the initiation of this trial
Secondary Outcome Measure Information:
Title
smoking reduction more than 50% and 25%
Time Frame
8 weeks after the initiation of this trial

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Competent volunteers completing consent form Schizophreniform, schizoaffective,or psychotic disorder NOS based on DSMIV Exclusion Criteria: Severe life-threatening physical condition Pregnancy Fluroxamine treatment in the past 2 weeks Allergy to nicotine or caffeine
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tsuo-Hung Lan, MD, Ph.D
Organizational Affiliation
General Clinical Research Center, YuLi hospital
Official's Role
Study Director
Facility Information:
Facility Name
Yuli hospital, DOH
City
Yuli Townhsip
ZIP/Postal Code
981
Country
Taiwan

12. IPD Sharing Statement

Learn more about this trial

The Pharmacogenetic Study , Readiness to Change, and Pharmacological Intervention for Smoking Cessation in Schizophrenia

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