SchizophreniaNCT00302432
The Effect of Cigarette Holders, Plastic Menthol Cigarettes, and Cognitive Behavioral Therapy for Smoking Reduction Among Schizophrenia Inpatients: A Comparative Study
A study testing Behavior therapy, cigarette holders, Flowers Menthol in people with Schizophrenia and Heavy Smoking, run by Lev-Hasharon Mental Healtlh Center at 1 site in Israel.
Trial summary
This study aims: 1. to assess the effect of smoking reduction programs (behavior therapy alone or behavior therapy with cigarette holders; "Flowers Menthol" plastic cigarettes with menthol) on cigarette smoking habits in an antipsychotic treated schizophrenia population. Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Schizophrenia, Heavy Smoking
- What is being tested?
- Behavior therapy, cigarette holders, Flowers Menthol
- Type of treatment
- Lifestyle or therapy programme
- How many people
- 37 participants
- Where
- 1 siteIsrael
- Study dates
- Mar 2006to Dec 2007
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Age 18-65 male or female.
- DSM -IV criteria for chronic schizophrenia or schizoaffective disorder.
- Ability and willingness to sign informed consent for participation in the study.
- Patients' expressed interest in participating in a smoking-reduction program
- Smoking a minimum of 20 cigarettes daily, for 6 months prior to the study period, as per patient report.
- Patients treated with antipsychotic agents.
Who cannot join
- Significant physical illness.
- Evidence of organic brain damage , mental retardation , alcohol or drug abuse.
- Pregnant or nursing female patients.
Trial locations and contacts
1 site in 1 country.
About this study
This study aims:
- to assess the effect of smoking reduction programs (behavior therapy alone or behavior therapy with cigarette holders; "Flowers Menthol" plastic cigarettes with menthol) on cigarette smoking habits in an antipsychotic treated schizophrenia population.
Read the detailed description
Smoking is a leading preventable cause of death in the western world. The highest incidence of smoking is among psychiatric inpatients. The issue of smoking among psychiatric patients needs to be addressed, since this population already suffers from physical comorbidity and reduced life expectancy (Brown et al., 2000), which increase with smoking, considering the additional risk factors for cardiovascular diseases: obesity, high cholesterol, diabetes. In addition the increased risk factors associated with second generation antipsychotic treatment need to be considered. Significant financial expenditures for the purchase of cigarettes, from an already extremely limited budget (Steinberg et al., 2004) should be taken into account. Psychiatric patients who smoke spend up to 30% of their welfare payments on cigarettes.
A survey performed in our mental health center revealed that over 30% of the patients who smoke are interested in specific treatment to reduce/stop smoking (Melamed et al., unpublished). Our survey found that The expressed desire of the patients to quit smoking and the known dangers of smoking, especially in this population, reflect the importance of integrating smoking reduction/cessation programs into the treatment regimens of psychiatric inpatients.
Treatment options to promote smoking cessation include hypnosis (Spiegel et la., 1993; Weizman et al., 2004), behavior therapy (Addington et al., 1998), group therapy (Addington, 1998), nicotine replacement therapies (NRT) (Fant et al., 2000), and pharmacotherapy such as bupropion (George et al., 2002).
Since it is recommended that many smoking cessation treatment options such as NRT (nicotine transdermal patches or nicotine polacrilex gum, nasal spray, cigarette filters and nicotine inhalers) should not be used together with actual nicotine intake we decided to gradually introduce the issue of smoking reduction/cessation to the inpatient population, by initially introducing a program for smoking reduction.
Smoking reduction options include:
- Cigarette holders
- "Flowers Menthol"
- Behavior therapy, including various relaxation techniques
Methods Study population: 60 subjects will be drawn from the inpatient population of Lev-Hasharon Mental Health Center, and divided into 4 groups of 15 participants each.
Inclusion criteria
- Age 18-65 male or female.
- DSM -IV criteria for chronic schizophrenia or schizoaffective disorder.
- Ability and willingness to sign informed consent for participation in the study.
- Patients' expressed interest in participating in a smoking-reduction program
- Smoking a minimum of 20 cigarettes daily, for 6 months prior to the study period, as per patient report.
- Patients treated with antipsychotic agents. Exclusion criteria
1- Significant physical illness. 2- Evidence of organic brain damage , mental retardation , alcohol or drug abuse.
3- Contraindication to amantadine treatment. 4- Pregnant or nursing female patients.
Duration of study will be 6 weeks. Patients will be assigned to one of 4 the intervention groups. Group assignment will be according to the department where the patient is hospitalized.
Group 1 - Behavior therapy only Group 2 - Behavior therapy with cigarette holders Group 3 - Behavior therapy with "Flowers Menthol" There will be no restrictions regarding the type of antipsychotic medication (typical or atypical) that participants are currently treated with.
Proposed study duration is 6 weeks. All patients will participate in 5 weekly behavioral group therapy sessions for smoking reduction. Each department will have a staff member devoted to smoking reduction "smoking supervisors" , who will accompany the patients throughout the week, advising, counseling, and supporting during crises.
Group 1 will have behavioral group therapy for smoking reduction, with not additional intervention.
Group 2 will be administered plastic cigarette holders. The nursing staff will distribute the holders one at a time. Used holders will be returned to the "smoking supervisor" when the sieve is blocked (usually after five cigarettes).
Group 3 will be administered Flowers Menthol (smokeless inhalers), one per day, by the "smoking supervisor". Used devices will be returned to him/her.
After receiving a detailed explanation of study procedures patients will sign informed consent. Throughout the study period, cigarettes will be distributed freely. Participants will fill out tables recording the number of cigarettes smoked, with the help of their "smoking supervisors".
Instruments
Patients will be assessed at baseline, and end of week 6 with the following instruments:
Clinical Rating Scales The patients' mental condition will be assessed with the Positive and Negative Syndrome Scale (PANSS) (Kay et al, 1987), Clinical Global Impression (CGI) scale for psychosis (Guy,1976), Hamilton Rating Scale for Depression (HAM-D) (Hamilton,1960), Simpson Angus Scale for extrapyramidal side effects (SAS) (Simpson and Angus 1970). Assessment of smoking dependence The Fagerstrom Tolerance Questionnaire for Nicotine Dependence (FTND Fagerstrom KO 1978) is useful and simple to administer for the evaluation of nicotine dependence.
Weekly table for self-report of the number of cigarettes smoked will be filled out by participants with the help of the "smoking supervisors".
Subjective Quality of Life Quality of life enjoyment and satisfaction questionnaire -abbreviated version (Q-LES-Q-18) (Ritsner et al., 2005).
Statistical analysis Appropriate statistical analysis will be performed including ANOVA with repeated measures.
- Conditions
- Schizophrenia, Heavy Smoking
- Being tested
- Behavior therapy, cigarette holders, Flowers Menthol
- Keywords
- smoking reduction, group therapy, cigarette holders, "Flowers Menthol"
- Medical subject headings
- Schizophrenia, Smoking Reduction
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Behavior therapy, cigarette holders, Flowers MentholBehavioural
What is being measured
The primary outcome is the main question the study is designed to answer.
Assessment of smoking dependence:
Measured: 6 weeks
The Fagerstrom Tolerance Questionnaire for Nicotine Dependence (FTND)
Measured: 6 weeks
Weekly table for self-report of the number of cigarettes smoked will be filled out by participants with the help of the "smoking supervisors".
Measured: 6 weeks
Subjective Quality of Life:
Measured: 6 weeks
Quality of life enjoyment and satisfaction questionnaire -abbreviated version
Measured: 6 weeks
Secondary outcomes (5)
Clinical Rating Scales:
Measured: 6 weeks
Positive and Negative Syndrome Scale (PANSS)
Measured: 6 weeks
Clinical Global Impression (CGI) scale for psychosis
Measured: 6 weeks
Hamilton Rating Scale for Depression (HAM-D)
Measured: 6 weeks
Simpson Angus Scale for extrapyramidal side effects (SAS)
Measured: 6 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 Mar 2006 (estimated)
- Study startMar 2006
- Primary completionDec 2007
- Study completionDec 2007
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for SchizophreniaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 37 participants (actual)
Sponsor and investigators
- Lead sponsor
- Lev-Hasharon Mental Healtlh Center
- Sponsor type
- Other government
- Investigators
- Dmitri Rudinski, MD, Principal investigator, Lev-Hasharon MHCYuval Melamed, MD, MHA, Study director, Lev-Hasharon MHCOlga Preisman, MD, Study chair, Lev-Hasharon MHCDeby Peres, MD, Study chair, Lev-Hasharon.MHCMarc Gelkopf, Phd, Study chair, Lev-Hasharon MHCSigalit Noam, RN, BA, Study chair, Lev-Hasharon MHCArturo Lerner, MD, Study chair, Lev-Hasharon MHCAvi Bleich, MD, MPH, Study director, Lev-Hasharon MHC
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00302432
- Sponsor's protocol ID
- LH16/2005.CTIL
- Status last verified
- Jul 2010
- First submitted
- 13 Mar 2006
- Last updated
- 22 Jul 2010
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 22 Jul 2010. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Cigarette Holders, Plastic Menthol Cigarettes, and Cognitive Behavioral Therapy for Smoking Reduction Among Schizophrenia Inpatients: A Comparative Study
- ClinicalTrials.gov ID
- NCT00302432
- Acronym / sponsor ID
- LH16/2005.CTIL
- Conditions
- Schizophrenia, Heavy Smoking
- Keywords
- smoking reduction, group therapy, cigarette holders, "Flowers Menthol"
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 37 participants (actual)
- Lead sponsor
- Lev-Hasharon Mental Healtlh CenterOther government
- Study start
- Mar 2006
- Primary completion
- Dec 2007 (actual)
- Study completion
- Dec 2007 (actual)
- First posted
- 14 Mar 2006 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study aims:
- to assess the effect of smoking reduction programs (behavior therapy alone or behavior therapy with cigarette holders; "Flowers Menthol" plastic cigarettes with menthol) on cigarette smoking habits in an antipsychotic treated schizophrenia population.
Detailed description
Smoking is a leading preventable cause of death in the western world. The highest incidence of smoking is among psychiatric inpatients. The issue of smoking among psychiatric patients needs to be addressed, since this population already suffers from physical comorbidity and reduced life expectancy (Brown et al., 2000), which increase with smoking, considering the additional risk factors for cardiovascular diseases: obesity, high cholesterol, diabetes. In addition the increased risk factors associated with second generation antipsychotic treatment need to be considered. Significant financial expenditures for the purchase of cigarettes, from an already extremely limited budget (Steinberg et al., 2004) should be taken into account. Psychiatric patients who smoke spend up to 30% of their welfare payments on cigarettes.
A survey performed in our mental health center revealed that over 30% of the patients who smoke are interested in specific treatment to reduce/stop smoking (Melamed et al., unpublished). Our survey found that The expressed desire of the patients to quit smoking and the known dangers of smoking, especially in this population, reflect the importance of integrating smoking reduction/cessation programs into the treatment regimens of psychiatric inpatients.
Treatment options to promote smoking cessation include hypnosis (Spiegel et la., 1993; Weizman et al., 2004), behavior therapy (Addington et al., 1998), group therapy (Addington, 1998), nicotine replacement therapies (NRT) (Fant et al., 2000), and pharmacotherapy such as bupropion (George et al., 2002).
Since it is recommended that many smoking cessation treatment options such as NRT (nicotine transdermal patches or nicotine polacrilex gum, nasal spray, cigarette filters and nicotine inhalers) should not be used together with actual nicotine intake we decided to gradually introduce the issue of smoking reduction/cessation to the inpatient population, by initially introducing a program for smoking reduction.
Smoking reduction options include:
- Cigarette holders
- "Flowers Menthol"
- Behavior therapy, including various relaxation techniques
Methods Study population: 60 subjects will be drawn from the inpatient population of Lev-Hasharon Mental Health Center, and divided into 4 groups of 15 participants each.
Inclusion criteria
- Age 18-65 male or female.
- DSM -IV criteria for chronic schizophrenia or schizoaffective disorder.
- Ability and willingness to sign informed consent for participation in the study.
- Patients' expressed interest in participating in a smoking-reduction program
- Smoking a minimum of 20 cigarettes daily, for 6 months prior to the study period, as per patient report.
- Patients treated with antipsychotic agents. Exclusion criteria
1- Significant physical illness. 2- Evidence of organic brain damage , mental retardation , alcohol or drug abuse.
3- Contraindication to amantadine treatment. 4- Pregnant or nursing female patients.
Duration of study will be 6 weeks. Patients will be assigned to one of 4 the intervention groups. Group assignment will be according to the department where the patient is hospitalized.
Group 1 - Behavior therapy only Group 2 - Behavior therapy with cigarette holders Group 3 - Behavior therapy with "Flowers Menthol" There will be no restrictions regarding the type of antipsychotic medication (typical or atypical) that participants are currently treated with.
Proposed study duration is 6 weeks. All patients will participate in 5 weekly behavioral group therapy sessions for smoking reduction. Each department will have a staff member devoted to smoking reduction "smoking supervisors" , who will accompany the patients throughout the week, advising, counseling, and supporting during crises.
Group 1 will have behavioral group therapy for smoking reduction, with not additional intervention.
Group 2 will be administered plastic cigarette holders. The nursing staff will distribute the holders one at a time. Used holders will be returned to the "smoking supervisor" when the sieve is blocked (usually after five cigarettes).
Group 3 will be administered Flowers Menthol (smokeless inhalers), one per day, by the "smoking supervisor". Used devices will be returned to him/her.
After receiving a detailed explanation of study procedures patients will sign informed consent. Throughout the study period, cigarettes will be distributed freely. Participants will fill out tables recording the number of cigarettes smoked, with the help of their "smoking supervisors".
Instruments
Patients will be assessed at baseline, and end of week 6 with the following instruments:
Clinical Rating Scales The patients' mental condition will be assessed with the Positive and Negative Syndrome Scale (PANSS) (Kay et al, 1987), Clinical Global Impression (CGI) scale for psychosis (Guy,1976), Hamilton Rating Scale for Depression (HAM-D) (Hamilton,1960), Simpson Angus Scale for extrapyramidal side effects (SAS) (Simpson and Angus 1970). Assessment of smoking dependence The Fagerstrom Tolerance Questionnaire for Nicotine Dependence (FTND Fagerstrom KO 1978) is useful and simple to administer for the evaluation of nicotine dependence.
Weekly table for self-report of the number of cigarettes smoked will be filled out by participants with the help of the "smoking supervisors".
Subjective Quality of Life Quality of life enjoyment and satisfaction questionnaire -abbreviated version (Q-LES-Q-18) (Ritsner et al., 2005).
Statistical analysis Appropriate statistical analysis will be performed including ANOVA with repeated measures.
Study design
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Age 18-65 male or female.
- DSM -IV criteria for chronic schizophrenia or schizoaffective disorder.
- Ability and willingness to sign informed consent for participation in the study.
- Patients' expressed interest in participating in a smoking-reduction program
- Smoking a minimum of 20 cigarettes daily, for 6 months prior to the study period, as per patient report.
Key exclusion criteria (3 listed)
- Significant physical illness.
- Evidence of organic brain damage , mental retardation , alcohol or drug abuse.
- Pregnant or nursing female patients.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Behavior therapy, cigarette holders, Flowers Menthol | Behavioural | – |
Primary outcome
Assessment of smoking dependence:
Time frame: 6 weeks
The Fagerstrom Tolerance Questionnaire for Nicotine Dependence (FTND)
Time frame: 6 weeks
Weekly table for self-report of the number of cigarettes smoked will be filled out by participants with the help of the "smoking supervisors".
Time frame: 6 weeks
Subjective Quality of Life:
Time frame: 6 weeks
Quality of life enjoyment and satisfaction questionnaire -abbreviated version
Time frame: 6 weeks
5 secondary outcomes
Clinical Rating Scales:
Time frame: 6 weeks
Positive and Negative Syndrome Scale (PANSS)
Time frame: 6 weeks
Clinical Global Impression (CGI) scale for psychosis
Time frame: 6 weeks
Hamilton Rating Scale for Depression (HAM-D)
Time frame: 6 weeks
Simpson Angus Scale for extrapyramidal side effects (SAS)
Time frame: 6 weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Jul 2010.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Dmitri Rudinski, MD principal investigator
Lev-Hasharon MHC
Yuval Melamed, MD, MHA study director
Lev-Hasharon MHC
Olga Preisman, MD study chair
Lev-Hasharon MHC
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Behavior therapy, cigarette holders, Flowers Menthol in people with Schizophrenia and Heavy Smoking, run by Lev-Hasharon Mental Healtlh Center at 1 site in Israel.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 22 Jul 2010. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Israel. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Assessment of smoking dependence: (time frame: 6 weeks). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Jul 2010.