Physical Activity in Promoting Smoking Cessation in African Americans (NCT01915810) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Physical Activity in Promoting Smoking Cessation in African Americans
United States45 participantsStarted 2014-01-29
Plain-language summary
This randomized pilot clinical trial studies the use of physical activity in promoting the discontinuation of the habit of smoking (smoking cessation) in African Americans. Participating in physical activity during an actual smoking quit attempt may work better in helping African Americans stop smoking.
Who can participate
Age range
21 Years – 65 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Self-reported African-American race
* Current daily smoker (has smoked \>= 100 cigarettes in lifetime per self-report, smoked \>= 5 cigarettes per day for the last 6 months per self-report)
* Self-reports motivation to quit smoking within the next 2 weeks
* Reports willingness to engage in a physical activity-based smoking cessation intervention
* Has a home address and a functioning home and/or cell phone number
* Able to engage in moderate intensity physical activity as determined by the Physical Activity Readiness Questionnaire (PAR-Q) or by physicians clearance (letter from physician or nurse practitioner) if currently taking medication for blood pressure or diabetes
* Willingness to wear the nicotine patches provided in the study as recommended
* Have an expired carbon monoxide (CO) level \> 8 parts per million (ppm) suggestive of current smoking
* Blood pressure =\< 140/90mm or by physicians clearance (letter from physician or nurse practitioner) if blood pressure reading \> 140/90mm Hg
Exclusion Criteria:
* Contraindication for nicotine patch use
* Regular use of tobacco products other than cigarettes in the last 30 days (including black \& milds)
* Current or planned future use of any nicotine replacement or pharmacological product for smoking cessation other than the study patches
* Pregnancy or lactation
* Another household member enrolled in the study
* A schedule not accommodating to the study procedures, or unwillingness to adhere to the …
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Recruitment feasibility, defined as >= 75% of eligible/screened participants choose to enroll in the study
Timeframe: Up to 8 weeks
2
Retention feasibility, defined as an overall retention rate of 80% and if each enrolled participant completes >= 66.7% of study visits (>= 6 of 9 study visits)