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Oral Nicotine Pouch Marketing Features Influence on Perceptions

Johns Hopkins Bloomberg School of Public Health logo

Johns Hopkins Bloomberg School of Public Health

Status

Invitation-only

Conditions

Tobacco Use

Treatments

Other: Discrete
Other: Convenient
Other: Tobacco-free

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06605924
R01DA055962 (U.S. NIH Grant/Contract)
IRB00029102

Details and patient eligibility

About

This study tests the effects of three oral nicotine marketing features on product perceptions.

Enrollment

5,000 estimated patients

Sex

All

Ages

13 to 120 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Live in the US
  • For youth age <21: Never used any nicotine pouch
  • For adults: Smoked greater than or equal to 100 cigarettes in during lifetime
  • For adults: Currently smoke some or all days
  • For adults: No regular use of oral nicotine pouches
  • For adults: No past 30-day pouch use

Exclusion criteria

  • Do not live in the US
  • For youth age <21: Ever used nicotine pouches
  • For youth age <21: Greater than or equal to 100 lifetime uses of any other nicotine or tobacco product
  • For adults: Smoked <100 cigarettes in life
  • For adults: Does not currently smoke some or all days
  • For adults: Regular use of oral nicotine pouches
  • For adults: Past 30-day pouch use

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

5,000 participants in 4 patient groups

Tobacco-free
Experimental group
Description:
Viewing a static advertisement
Treatment:
Other: Tobacco-free
Discrete
Experimental group
Description:
Viewing a static advertisement
Treatment:
Other: Discrete
Convenient
Experimental group
Description:
Viewing a static advertisement
Treatment:
Other: Convenient
Control
No Intervention group
Description:
Viewing a static advertisement - baseline language only

Trial contacts and locations

1

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Central trial contact

Meghan Moran, PhD; Maryam Ibrahim, BA

Data sourced from clinicaltrials.gov

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