Working Memory Training on Delay Discounting Among Cigarette Smokers
Tobacco Use Disorder/Cigarette Smoking
Bottom Line
View on ClinicalTrials.gov: NCT05210608 ↗Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Working Memory Training + Behavioral Intervention (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of Kansas Medical Center
- Primary completion
- Jun 2022
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Delay Discounting |
-5.21; -6.57; -7.13 | .29 |
| PRIMARY Timeline Follow-Back (TLFB): Number of Total Cigarettes Smoked Per Week |
76.53; 38.83; 59.50 | =0.015 sig |
| PRIMARY Carbon Monoxide Levels |
17.70; 17.67; 30 | .90 |
| PRIMARY Working Memory |
58.61; 61.33; 71.25 | .18 |
Summary
Eligibility Criteria
Inclusion criteria: To be included in this study, a participant must be 18 years of age or older, who have smoked at least four cigarettes per day for at least 6 months, are interested in quitting cigarette smoking, are at or below the federal poverty line based on persons in family/household and annual household income:
- 1 -- $12,880
- 2 -- $17,420
- 3 -- $21,960
- 4 - $26,500
- 5 -- $31,040
- 6 -- $35,580
- 7 -- $40,120
- 8 -- $44,660
- 9 - add $4, 540 for each additional person,
OR they or their child(ren) utilize a federal program for low-income individuals, and are willing to participate in a 5-week working memory training program as a pretreatment adjunct to behavioral group + nicotine replacement therapy (NRT; via nicotine patches).
Exclusion criteria: Participants must not indicate a severe substance use disorder according to the DSM-V with any substance other than tobacco or have any significant medical or psychiatric condition. Such conditions could include traumatic brain injury, dementia, significant learning disability, or psychotic symptoms. Participants must be at least at a 5th-grade reading level. In case that participants are excluded, they will be provided with resources in the community and provided with contact information for the Kansas Tobacco Quitline.
Data sourced from ClinicalTrials.gov (NCT05210608). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.