The current project has two main objectives:Research question 1 (RQ1): Is the transition from experimental to dependent smoking in high-risk adolescents predicted by the strength of goal-directed and impulse control systems as well as habit…
ID
Source
Brief title
Condition
- Other condition
Synonym
Health condition
nicotine dependence
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The main study parameter for RQ1 is the number of smoked cigarettes per day at
baseline, 6, and 12-month follow-up. The main study parameter for RQ2 is brain
activation in the ventral and dorsal striatum in response to smoking cues at
baseline and at 1-year follow-up. Inclusion of participants will end when the
planned number of participants finished the first EMA and baseline
measurements. The study will end when the planned number of participants
finished all study procedures.
Secondary outcome
- Fagerström test for Nicotine Dependence (FTND) to measure nicotine
dependence.
- Hooked on nicotine checklist (HONC) to measure the development of symptoms of
nicotine dependence.
- The Autonomy Over Tobacco Scale (AOTS) to assess autonomy over smoking and
cue-induced craving.
- Self - Report Habit Index (SRHI) to measure habit behaviour regarding
smoking.
- Pleasure of smoking questionnaire (PSQ) to measure to which extend
participants experience pleasure from smoking.
- Task performance on tthe digit span test and the Two-Step task
Background summary
Despite serious well-known health risks, 31% of Dutch adolescents have tried
smoking, and 21% of 18 year olds smoke on a daily basis. While various
addiction models explain the continuation of substance dependence, the
transition from experimental to dependent substance use remains largely
unexplained. The current project aims to bridge this gap by developing a
neurocognitive model describing the mechanisms critically involved in the
transition from experimental to dependent smoking in low educated high-risk
adolescents.
Study objective
The current project has two main objectives:
Research question 1 (RQ1): Is the transition from experimental to dependent
smoking in high-risk adolescents predicted by the strength of goal-directed and
impulse control systems as well as habit propensity? It is hypothesized that
experimental smokers with a stronger habit propensity and weaker goal-directed
and impulse control systems are more likely to develop nicotine dependence.
Research question 2 (RQ2): Is the transition from experimental to dependent
smoking associated with a shift from goal directed behaviour through positive
reinforcement (i.e., activation in the ventral striatum to smoking cues) to a
habitual response (i.e., activation in the dorsal striatum to smoking cues)? It
is hypothesized that transition into dependent smoking is associated with a
shift from ventral to dorsal striatal reactivity to smoking cues in a smoking
cue-reactivity paradigm.
Study design
A three-wave longitudinal study design will be employed. At baseline and at
1-year follow-up all the relevant brain systems will be measured using fMRI.
Additionally, smoking behaviour will be measured using ecological momentary
assessments (EMA) at baseline. An online questionnaire about smoking behavior
will completerd 6 months after the baseline measurements by the experimental
smokers. This longitudinal design allows us to use baseline fMRI measures to
predict the development of smoking behaviour over a 1-year time period. At
1-year follow-up, all relevant brain systems will be measured again to answer
RQ2. For this aim brain activation at baseline and 1-year follow-up will be
compared in those participants who develop nicotine dependence. A control group
of non-smokers will be included to investigate baseline differences in brain
activation between experimental smokers and non-smokers in order to contribute
to the development of a neurocognitive developmental model of addiction.
Study burden and risks
For the current study, participants will complete (online) questionnaires,
perform cognitive tasks on a computer and will undergo an MRI scanning session
two times. MRI measurements themselves do not pose any risk, with regards to
possible physical risks, if appropriate precautions are made. Furthermore
participation in the current study will only cause limited burden. No benefits
are related to participation in the current study. The inclusion of 12-18 years
old participants is necessary given that smoking is generally initiated during
this age period, especially in high-risk populations such as students following
low-education levels. Overall, we feel that the knowledge we gain through this
project, as well as the risk-free nature of this study, justifies the efforts
of the participants. The control group will only complete fMRI baseline
measures and cognitive tasks and questionnaires at baseline.
Montessorilaan 3
Nijmegen 6525 HR
NL
Montessorilaan 3
Nijmegen 6525 HR
NL
Listed location countries
Age
Inclusion criteria
Experimental smokers
1) Smoked 5-500 cigarettes lifetime
2) Smoked in the last 6 months
3) Never smoked on a daily basis;Controls
1) Never smoked a complete cigarette;All participants
1) Age 12-18
Exclusion criteria
All participants
1) Use of psychoactive medication that cannot be stopped for 24 hours before scanning
2) fMRI contraindications
3) A history of neurological disease
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL57111.091.16 |