Effects of Nicotine Reduction on Smoking Behavior in ADHD Smokers
NCT ID: NCT02599571
Last Updated: 2020-01-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
71 participants
INTERVENTIONAL
2016-03-30
2019-09-12
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
BASIC_SCIENCE
DOUBLE
Study Groups
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Very low nicotine content cigarettes
Reduced nicotine content cigarettes.
Very low nicotine content cigarettes
Cigarettes containing a reduced amount of nicotine
Conventional nicotine content cigarettes
Cigarettes containing a normal amount of nicotine
Conventional nicotine content cigarettes
Conventional nicotine content cigarettes.
Very low nicotine content cigarettes
Cigarettes containing a reduced amount of nicotine
Conventional nicotine content cigarettes
Cigarettes containing a normal amount of nicotine
Interventions
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Very low nicotine content cigarettes
Cigarettes containing a reduced amount of nicotine
Conventional nicotine content cigarettes
Cigarettes containing a normal amount of nicotine
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Smoke an average of 5-40 cigarettes per day for at least 1 year
* Breath CO levels \> 8 ppm (if ≤ 8 ppm, then NicAlert Strip \> 6)
* Primary diagnosis of ADHD, any subtype as assessed by the CAADID; T-Score \> 65 on one of the DSM- V relevant scales (Inattentive Symptoms, Hyperactive-Impulsive Symptoms, Total Symptoms or ADHD Index) on the Self-Report version of the CAARS; Clinician Rated ADHD-RS score \>24.
* Cognitive functioning \> 80 as assessed by the KBIT-II
Exclusion Criteria
* Currently seeking treatment for smoking cessation
* Currently using nicotine replacement therapies or other pharmacotherapies as cessation aid (intermittent use acceptable)
* A quit attempt in the past 30 days resulting in greater than 3 days of abstinence
* Using other tobacco products more than 9 days in the past 30 days
* Significant unstable medical conditions (any significant change in a serious medical condition occurring during the past 3 months including cardiovascular disease, COPD, and cancer, as determined by the study physician at each site)
* Significant unstable psychiatric conditions (any significant change in psychiatric symptoms during the past 3 months as determined by the study physician at each site)
* Any Axis I Psychiatric Disorder as assessed by the MINI that is significantly impairing and/or would contraindicate participation in the study
* Psychiatric medication changes in the past 3 months including new prescriptions, changes in dosages or discontinuation of medications
* Positive toxicology screen for any of the following drugs: cocaine, opiates, methadone, benzodiazepines, barbiturates, amphetamines, methamphetamines, and PCP (Marijuana will be tested for but will not be an exclusionary criterion, participants with valid prescriptions for opiates, benzodiazepines, barbiturates, amphetamines or methadone will not be excluded, participants failing the toxicology screen will be allowed to re-screen once. These participants will need to be re-consented before being rescreened to ensure they have received adequate informed consent.)
* Breath alcohol level \> 0.01 (Participants failing the breath alcohol screen will be allowed to re-screen once. These participants will need to be re-consented before being rescreened to ensure they have received adequate informed consent.)
* Current diagnosis of DSM alcohol or drug use disorder (except for nicotine)
* Pregnant, trying to become pregnant or breastfeeding
* Smoking 'roll your own cigarettes' exclusively
* Currently taking anticonvulsant medications including: Phenytoin \[Brand Name: Dilantin\], Carbamazepine \[Brand Name: Tegretol, Carbatrol, Equetro, Epitol\], Oxcarbazepine \[Brand Name: Trileptal\], Primidone \[Brand Name: Mysoline\], Phenobarbital
* CO reading \>80 ppm
* Systolic BP between 90 and 160 (If below 90 then asymptomatic. Participants failing for blood pressure will be allowed to re-screen once.)
* Diastolic BP between 50 and 100 (If below 50 then asymptomatic. Participants failing for blood pressure will be allowed to re-screen once.)
* Heart rate between 45 and 115 bpm (If below 45 then asymptomatic. Participants failing for heart rate will be allowed to re-screen once.)
* Indicating any suicidal ideation in the past month or suicide attempts in the past 10 years.
* Inability to independently read and comprehend the consent form and other written study materials and measures.
* Having participated in a research study during the past three months in which the participant: Smoked a cigarette that was not his/her usual brand cigarette for more than one day, used any tobacco products beyond normal use for more than one day, used any nicotine replacement products or smoking cessation medications for more than one day
* Any previous experience using SPECTRUM cigarettes
18 Years
40 Years
ALL
Yes
Sponsors
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Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
NIH
Food and Drug Administration (FDA)
FED
University of Pittsburgh
OTHER
Duke University
OTHER
Responsible Party
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Principal Investigators
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Scott Kollins, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
Duke ADHD Program
Locations
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Duke University Medical Center
Durham, North Carolina, United States
University of Pittsburgh
Pittsburgh, Pennsylvania, United States
Countries
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Other Identifiers
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Pro00066144
Identifier Type: -
Identifier Source: org_study_id
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