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Investigation of Cigarette Cravings in Smokers

M

Marco Leyton

Status

Unknown

Conditions

Addiction Nicotine
Cigarette Smoking
Tobacco Use

Treatments

Behavioral: Cue induction
Behavioral: Control stress exposure
Behavioral: Neutral cue exposure
Behavioral: Stress induction

Study type

Interventional

Funder types

Other

Identifiers

NCT04843969
421-0318

Details and patient eligibility

About

Interventions to disrupt memory reconsolidation have held promise for the treatment of stress- and anxiety-related disorders. In the present study, the investigators will examine whether an intervention based on these principles, called memory updating, could be adapted for reward-seeking behaviors. To test this, non-treatment seeking tobacco smokers will be exposed to smoking cues and/or stress, two stimuli known to trigger smoking. It is predicted that exposure to a stress task will enhance the cues' motivational salience and yield greater susceptibility to the memory updating procedure.

As an add-on, the investigators will examine COVID-associated changes in substance use and whether participants in the memory updating groups might be more resilient to these effects. It is predicted that the changes in substance use will depend on whether the substances are used primarily in social settings.

Full description

Non-treatment seeking cigarette dependent smokers will be randomized to one of four testing conditions: 1) a non-stressful task followed by neutral cues, 2) the non-stressful task followed by smoking cues, 3) a stressful task followed by neutral cues, or 4) the stressful task followed by smoking cues. Ten minutes after the intervention, participants will undergo a 60-minute extinction procedure consisting of smoking-related videos, images and smoking paraphernalia. Cue reactivity test sessions will take place 24 hours, 2 weeks and 6 weeks following the intervention.

COVID-associated changes in substance use will be quantified over three telephone interviews: one at the end of March / beginning of April 2020 (at the start of the pandemic), one at the end of April / beginning of May, and a final one which will be instituted if feasible once the infection rates and social distancing policies have decreased.

Enrollment

76 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Scoring 5 or higher on the Fagerström Test for Cigarette Dependence
  • Willingness to abstain from smoking for 4 hours prior to each laboratory visit

Exclusion criteria

  • Currently using cigarette cessation products
  • Endocrinological problems
  • Significant mental or physical health conditions
  • Pregnancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

76 participants in 4 patient groups

Stress task and smoking cue
Experimental group
Description:
Exposure to a psychosocial stress task followed by smoking video cues
Treatment:
Behavioral: Stress induction
Behavioral: Cue induction
Stress task and neutral cue
Experimental group
Description:
Exposure to a psychosocial stress task followed by neutral video cues
Treatment:
Behavioral: Neutral cue exposure
Behavioral: Stress induction
Control task and smoking cue
Active Comparator group
Description:
Exposure to a control task followed by smoking video cues
Treatment:
Behavioral: Cue induction
Behavioral: Control stress exposure
Control task and neutral cue
Active Comparator group
Description:
Exposure to a control task followed by neutral video cues
Treatment:
Behavioral: Neutral cue exposure
Behavioral: Control stress exposure

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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