Carrot Inc.
Redwood City, California, 94063, United States
NCT Number: NCT04133064
Prospective open label, single center study enrolling up to 220 participants to evaluate the effect of the Pivot Breath Sensor on a user's attitudes towards quitting smoking and smoking behavior.
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Notify Me18 year–80 year
All sexes
Interventional
Not applicable
Redwood City, California, 94063, United States
Study to collect the following data during and after use of a personal carbon monoxide breath sensor (Pivot Breath Sensor):
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The Pivot Breath Sensor measures the level of carbon monoxide in exhaled breath and displays the carbon monoxide value to the user.
Time frame: 3 months (12 weeks) compared to baseline
Assessment of participant's desire to quit by measuring Stage of Change.
The participant will be asked if they are serious about quitting smoking and they can select from the following options:
Time frame: 3 months (12 weeks)
Assessment of participant's attitudes towards quitting by measuring Success to Quit.
The participant will be asked If you were to quit smoking right now, how successful would you be? Rating Scale: 1 = Not at all successful, 10 = Completely successful. Higher score is a better outcome for participants, it indicates a more positive attitude towards quitting smoking.
Time frame: 3 months (12 weeks)
Assessment of participant's attitudes towards quitting by measuring Perceived Difficulty to staying Quit.
Participant will be asked: If you were to quit smoking right now, how difficult do you think it would be to stay smoke free? Rating scale: 1 = Really hard to stay quit, 10 = Really easy to stay quit. Higher score is a better outcome for participants, it indicates a more positive attitude towards quitting smoking, specifically lower perceived difficulty to quit.
Time frame: 3 months (12 weeks)
Assess participant's smoking behavior by measuring Quit attempts. Participant were asked: Since you began using the Pivot Breath Sensor, how many times have you tried to quit smoking?
Time frame: 3 months (12 weeks)
Assess participant's smoking behavior by measuring CPD. Participant will be asked to enter a number for: How many cigarettes do you now smoke per day, on average? Enter number value.
Time frame: 3 months (12 weeks)
Assess participant's smoking behavior by measuring 7-Day and 30-Day PPA. Participant will be asked: In the last 7 days and 30 days have you smoked any cigarettes? Answer choice: Yes/No 7-Day PPA is defined as answering "No" to "In the last 7 days have you smoked any cigarettes?" 30-Day PPA is defined as answering "No" to "In the last 30 days have you smoked any cigarettes?" Data obtained via questionnaires completed by the participants.
Time frame: 1 week
Gather participant feedback on breath sensor setup:
Participant is asked:
Select one:
Time frame: 1 week
Gather participant feedback on impact of breath sensor:
Participant will be asked: How has using the breath sensor affected your motivation to quit smoking?
Select one:
Time frame: 1 week
Gather participant feedback on impact of breath sensor:
Participant will be asked: How has using the breath sensor affected the number of cigarettes you smoke per day?
Select one:
Time frame: 4 weeks
Gather participant feedback on commercialization:
Participant will be asked: Hypothetical: if it was commercially available, would you be interested in buying the Pivot Breath Sensor? Answer: Yes/No
Jennifer Marler, MD
Industry
Pivot Breath Sensor Study to Evaluate the Effect of the Pivot Breath Sensor on a User's Attitudes Towards Quitting Smoking and Smoking Behavior.
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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