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NCT Number: NCT05772845

Vaping and Smoking Withdrawal Project

The proposed research, which will systematically and comprehensively characterize the withdrawal among daily vapers compared to daily smokers of combustible cigarettes, filling critical gaps in the understanding of electronic nicotine delivery systems (ENDS) dependence/abuse liability and contributing to the development of therapies for tobacco/nicotine use, the leading preventable cause of death in the US.

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Key information

Age range

21 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University at Buffalo

Buffalo, New York, 14260, United States

Location status: Recruiting

Location contact

Larry Hawk, PhD

CONTACT

[email protected]

7166450192

About this study

Withdrawal is a key, multi-faceted component of tobacco/nicotine dependence. Because withdrawal symptoms are theorized to drive relapse, facets of withdrawal (e.g., craving, negative affect) are the targets of most current and emerging treatments. Despite the central importance of withdrawal, and a voluminous literature on withdrawal from combustible cigarette smoking, little is known about withdrawal from electronic nicotine delivery systems (ENDS). To overcome critical barriers to progress in the field, the first-ever prospective, controlled comparison of abstinence-induced withdrawal between ENDS vapers and cigarette smokers is proposed. Participants will be 160 established daily vapers (including former smokers and dual users who smoke occasionally), 160 established daily smokers (including former vapers and dual users who vape occasionally), and (for exploratory comparisons) 50 established daily dual users, who smoke and vape daily. Participants will complete two 4-hour lab visits; the order of the ad lib use visit and the abstinent visit (which follows 24 hours of abstinence) will be randomized across participants. To advance knowledge of ENDS withdrawal, state-of-the-science, multi-measure, multi-method assessments of key withdrawal facets (negative affect, craving, difficulty concentrating, restlessness, sleep, and appetite, as well as anhedonia/positive affect and somatic effects) will be employed. For each facet, the hypothesis that withdrawal magnitude is lower among vapers compared to smokers will be tested. To inform theory and intervention development, the behavioral significance of ENDS withdrawal will also be evaluated, testing the hypotheses that abstinence will increase the motivation to vape/smoke and this group difference will be accounted for (mediated) by vaper/smoker differences in one or more withdrawal facets. Exploratory analyses will examine whether group differences in withdrawal are accounted for (mediate) by differential nicotine exposure, explore the role of individual differences (e.g., sex, rate of nicotine metabolism, expectancies), and examine differences among sub-groups of vapers. The impact of this much-needed, detailed characterization of withdrawal from ENDS is enhanced by the inclusion of a comparator of great public health significance, cigarette smoking. In addition, by characterizing the specific withdrawal facets that drive motivation to vape/smoke, the proposed work will identify promising intervention targets for subsequent treatment development efforts.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 6+ months of daily/near-daily nicotine vaping and/or cigarette smoking (to yield 160 vapers, 160 smokers, 50 dual users)
  • 200+ ng/mL cotinine on a commercially-available quick screen

Current Exclusion Criteria:

  • intention to quit daily/near-daily vaping/smoking in the next month
  • current (2+ days out of the past 7) use of pipe tobacco, hookah/shisha, smokeless tobacco, dissolvable tobacco, nicotine pouches. For vaping group only, current (2+ days out of past 7) use of cigars, cigarillos, or filtered cigars that are filled with tobacco or a mix of tobacco and marijuana
  • current use of any smoking cessation medication
  • current severe substance dependence other than tobacco/nicotine (including cannabis; NIDA Modified ASSIST of 27+)
  • current (past 2 weeks) suicidal ideation with intent and/or plan
  • current antipsychotic medications or lifetime history of schizophrenia or bipolar disorder
  • pregnancy (intake urine screen)

Original Exclusion Criteria that have been modified or eliminated:

  • >1 use in past month of tobacco/nicotine products other than ENDS and combustible cigarettes (modified 5/19/25 - see current exclusion criteria)
  • alcohol: AUDIT > 15 for males and >13 for females (eliminated 7/25/23)
  • current major depression (PHQ-9>11) (eliminated 7/25/23)
  • suicide risk (answer to question #9 on PHQ-9 is anything other than "Not at all") (modified 11/17/23 - see current exclusion criteria)

Treatment and study plan

Acute (24-hour) abstinence

Behavioral

Participants will be asked to abstain from all tobacco/nicotine for 24 hours prior to the visit

Ad libitum smoking/vaping

Behavioral

Participants will be asked to smoke/vape as usual during the 24 hours prior to the visit

Primary outcomes

  1. Wisconsin Smoking Withdrawal Scale - anger 0.5

    Time frame: 0.5 hours

    anger subscale score

  2. Wisconsin Smoking Withdrawal Scale - anger 2.5

    Time frame: 2.5 hours

    anger subscale score

  3. Wisconsin Smoking Withdrawal Scale - anx 0.5

    Time frame: 0.5 hours

    anxiety subscale score

  4. Wisconsin Smoking Withdrawal Scale - anx 2.5

    Time frame: 2.5 hours

    anxiety subscale score

  5. Wisconsin Smoking Withdrawal Scale - sad 0.5

    Time frame: 0.5 hours

    sadness subscale score

  6. Wisconsin Smoking Withdrawal Scale - sad 2.5

    Time frame: 2.5 hours

    sadness subscale score

  7. Wisconsin Smoking Withdrawal Scale - conc 0.5

    Time frame: 0.5 hours

    difficulty concentrating subscale score

  8. Wisconsin Smoking Withdrawal Scale - conc 2.5

    Time frame: 2.5 hours

    difficulty concentrating subscale score

  9. Wisconsin Smoking Withdrawal Scale - sleep 0.5

    Time frame: 0.5 hours

    sleep subscale score

  10. Wisconsin Smoking Withdrawal Scale - sleep 2.5

    Time frame: 2.5 hours

    sleep subscale score

  11. Wisconsin Smoking Withdrawal Scale - appetite 0.5

    Time frame: 0.5 hours

    appetite subscale score

  12. Wisconsin Smoking Withdrawal Scale - appetite 2.5

    Time frame: 2.5 hours

    appetite subscale score

  13. Mood and Physical Symptoms Scale - 0.5

    Time frame: 0.5 hours

    single-item indicators of withdrawal facets

  14. Mood and Physical Symptoms Scale - 2.5

    Time frame: 2.5 hours

    single-item indicators of withdrawal facets

  15. Minnesota Nicotine Withdrawal Scale - 0.5

    Time frame: 0.5 hours

    17-item version with indicators of various withdrawal facets

  16. Minnesota Nicotine Withdrawal Scale - 2.5

    Time frame: 2.5 hours

    17-item version with indicators of various withdrawal facets

  17. Positive and Negative Affect Scale - PA 0.5

    Time frame: 0.5 hours

    positive affect subscale score

  18. Positive and Negative Affect Scale - PA 2.5

    Time frame: 2.5 hours

    positive affect subscale score

  19. Positive and Negative Affect Scale - NA 0.5

    Time frame: 0.5 hours

    negative affect subscale score

  20. Positive and Negative Affect Scale - NA 2.5

    Time frame: 2.5 hours

    negative affect subscale score

  21. Snaith-Hamilton Pleasure Scale 0.5

    Time frame: 0.5 hours

    total score

  22. Snaith-Hamilton Pleasure Scale 2.5

    Time frame: 2.5 hours

    total score

  23. Questionnaire on Vaping Craving 0.5

    Time frame: 0.5 hours

    total craving score

  24. Questionnaire on Vaping Craving 2.5

    Time frame: 2.5 hours

    total craving score

  25. Questionnaire on Smoking Urges - Brief 0.5

    Time frame: 0.5 hours

    total craving score

  26. Questionnaire on Smoking Urges - Brief 2.5

    Time frame: 2.5 hours

    total craving score

  27. PhenX Toolkit Insomnia Severity Index 0.5

    Time frame: 0.5 hours

    7-item scale (but item #5 is omitted because of the short time-frame), total score impairment and interference with daily functioning

  28. PhenX Toolkit Insomnia Severity Index 2.5

    Time frame: 2.5 hours

    7-item scale (but item #5 is omitted because of the short time-frame), total score impairment and interference with daily functioning

  29. Restlessness ratings 0.5

    Time frame: 0.5 hours

    3-item scale

  30. Restlessness ratings 2.5

    Time frame: 2.5 hours

    3-item scale

  31. Restlessness and Agitation Questionnaire - Modified 0.5

    Time frame: 0.5 hours

    total score on subset of behavioral indicators

  32. Restlessness and Agitation Questionnaire - Modified 2.5

    Time frame: 2.5 hours

    total score on subset of behavioral indicators

  33. Identical Pair Continuous Performance Task

    Time frame: ~2 hours

    Sustained attention, or vigilance, is the ability to maintain alertness to detect infrequent target stimuli during a long, monotonous task (e.g., Mackworth, 1948). We will use a version of the identical-pairs continuous performance task (Cornblatt et al., 1988) in which participants attend to a series of 800 4-digit numbers on a computer monitor (100-ms stimulus duration; 1500-ms ISI).

    Participants are asked to press the keyboard space bar only when the stimulus is identical to the immediately preceding stimulus (10% targets; Cooper et al., 2020; Rhodes & Hawk, 2016).

    Percent correct hits (target detections) is the primary outcome.

  34. n-back working memory task

    Time frame: ~2 hours

    The n-back task (e.g., Strand et al., 2012; Rhodes & Hawk, 2016) requires indicating whether each stimulus in a rapidly presented series matches the location of the stimulus presented n stimuli before (e.g., n=0,1,2). Stimuli are small grey circles (100 ms; 30% targets). The focus here is on conditions that place marked demands on the "central executive" by requiring ongoing mental manipulation (i.e., n=2; see Baddeley, 2003). Brief practice with a 1-back and 2-back will be followed by 2 100-trial blocks of the 2-back. Accuracy is the primary outcome.

  35. Stop signal reaction time task

    Time frame: ~2 hours

    We will employ the stop-signal paradigm (Logan et al., 1984), which provides a relatively pure index response inhibition (e.g., Nigg, 2001). In our typical task (e.g., Hawk et al., 2018; Rhodes & Hawk, 2016), participants button press to indicate whether the "go" signal (<-- or -->) is pointing left or right. After a brief "go" practice, the stop signal (100-ms tone) is introduced, and participants complete 3 64-trail bocks during with they are asked to respond as quickly as possible but to not respond on stop signal trials (25% of trials). The stop signal occurs after go signal onset and adjusts dynamically across trials to yield ~50% inhibition (Logan et al., 1997). The primary outcome is stop signal reaction time (SSRT), an estimate of the speed of inhibition.

  36. kcal consumed

    Time frame: 3 hours

    Fat, protein, and carbohydrate calories, and total calories, consumed during the visit.

  37. Hypothetical commodity purchase task - vaping intensity 0.5

    Time frame: 0.5 hours

    Intensity of demand

  38. Hypothetical commodity purchase task - vaping intensity 2.5

    Time frame: 2.5 hours

    intensity of demand

  39. Hypothetical commodity purchase task - vaping persistence 0.5

    Time frame: 0.5 hours

    persistence of demand

  40. Hypothetical commodity purchase task - vaping persistence 2.5

    Time frame: 2.5 hours

    persistence of demand

  41. Hypothetical commodity purchase task - smoking intensity 0.5

    Time frame: 0.5 hours

    intensity of demand

  42. Hypothetical commodity purchase task - smoking intensity 0.5

    Time frame: 2.5 hours

    intensity of demand

  43. Hypothetical commodity purchase task - smoking persistence 0.5

    Time frame: 0.5 hours

    persistence of demand

  44. Hypothetical commodity purchase task - smoking persistence 2.5

    Time frame: 2.5 hours

    persistence of demand

  45. Choice Behavior Under Cued Conditions (CBUCC) Task - spend vape

    Time frame: 3 hours

    Spending for vape puffs

  46. Choice Behavior Under Cued Conditions (CBUCC) Task - spend cig

    Time frame: 3 hours

    Spending for cigarette puffs

  47. Choice Behavior Under Cued Conditions (CBUCC) Task - spend water

    Time frame: 3 hours

    Spending for water control

  48. Choice Behavior Under Cued Conditions (CBUCC) Task - crave vape

    Time frame: 3 hours

    Craving for vape puffs

  49. Choice Behavior Under Cued Conditions (CBUCC) Task - crave cig

    Time frame: 3 hours

    Craving for cigarette puffs

Secondary outcomes

  1. modified Cigarette evaluation questionnaire

    Time frame: 3.5 hours

    subjective/sensory aspects of smoking

  2. modified e-Cigarette evaluation questionnaire

    Time frame: 3.5 hours

    subjective/sensory aspects of vaping

  3. Heart rate

    Time frame: assessed at ~30-minute intervals

    Heart rate, in beats per minute

  4. Somatic/side effect checklist

    Time frame: 0.5 hours

    Assesses a range of somatic and psychological symptoms (e.g., headache, fatigue, anxiety)

  5. Somatic/side effect checklist

    Time frame: 2.5 hours

    Assesses a range of somatic and psychological symptoms (e.g., headache, fatigue, anxiety)

Other outcomes

  1. Cotinine

    Time frame: 0.25 hours

    assay cotinine from urine sample collected at the start of each visit in order to assess the degree of compliance with the abstinence manipulation

  2. Expired-air carbon monoxide

    Time frame: 0.25 hours

    biochemical measure related to past 24-hour smoking

Study contacts

Contact information is provided by the study sponsor or research team.

Larry Hawk, PhD

CONTACT

[email protected]

716-645-0192

Sponsors and collaborators

Lead sponsor

State University of New York at Buffalo

Other

Collaborators

  • National Institute on Drug Abuse (NIDA)
  • Roswell Park Cancer Institute

Registry information

Official study title

A Controlled Evaluation of Abstinence-Induced Withdrawal and Motivation to Vape/Smoke Among Daily ENDS Users vs. Cigarette Smokers

Acronym: VASP

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Mar 16, 2023
Registry last updated
Mar 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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