Smoking CessationQuit and FitNCT02103582
Quit and Fit: A Tobacco Cessation and Energy Balance Pilot for African Americans
A study testing Intervention in people with Smoking Cessation, run by Georgetown University at 1 site in United States.
Trial summary
The Quit \& Fit intervention will be designed as a 12-week study to promote smoking cessation, increase physical activity levels, and reduce weight gain through regular exercise and healthy nutrition for African American Women smokers. Read more about this study
- Who is it for?
- Ages 18 to 69 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Smoking Cessation
- What is being tested?
- Intervention
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 40 participants
- Where
- 1 siteUnited States
- Study dates
- Apr 2013to Nov 2017
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 69 years
- Women only
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- African American women ages 18-69;
- Currently smoke at least 5 cigarettes per day;
- Smoked daily for the past one year;
- Able to provide informed consent;
- Generally good health as determined by medical history;
- Able to participate in exercise training.
Who cannot join
- Women who are:
- Currently pregnant; or have
- heart disease,
- lung disease, or
- mental illness
Trial locations and contacts
1 site in 1 country.
United States1 site
Georgetown University Lombardi community site office
Washington D.C., District of Columbia, 20003
About this study
The Quit \& Fit intervention will be designed as a 12-week study to promote smoking cessation, increase physical activity levels, and reduce weight gain through regular exercise and healthy nutrition for African American Women smokers.
Patients will be assigned to the fitness intervention group or control groups by a computer.
Read the detailed description
- * Purpose of project (one or two sentences): The feasibility phase of the proposed study is comprised of a two-arm randomized pilot trial to evaluate the feasibility, satisfaction, and preliminary efficacy of 'Quit \& Fit'. Women (N=40) will receive 12 weekly smoking cessation telephone counseling sessions. Participants will be randomized to either a fitness intervention (Quit \& Fit) or a contact time control (Quit for Life).
- * Study design (for example, hypothesis, research questions, standard and experimental procedures/drugs/devices or equipment, etc.): The Quit \& Fit intervention will be designed as a 12-week, tailored multiple health outcome intervention to promote smoking cessation, achieve energy balance, and reduce post-cessation weight gain through regular PA and healthy nutrition for AAW smokers. Culturally tailored comprehensive interventions that address smoking-cessation and obesity/weight-control among AAW are needed. The conceptual basis of the proposal is Albert Bandura's social cognitive Theory (SCT), which posits that people learn through observation and modeling of behaviors, attitudes, and emotional reactions. When applied to smoking cessation and health behavior change, social learning can be viewed as a transition through stages of increased knowledge, self-efficacy, and social support, culminating in readiness to change behaviors. The SCT model allows for targeting of factors relevant to a given individual and tailoring messages to each each participant's cultural values. Participants will be randomized into one of the study groups: the 'control arm' or the 'exercise arm'. Both groups will receive 12 weeks of smoking cessation counseling, telephone counseling and and will receive 10 weeks of nicotine replacement therapy (NRT) in the form of nicotine lozenges. Participants who are randomized to the 'control arm' will be asked to maintain their current daily activities for 12 weeks. They will also be required to visit the study site 3 times per week for 12 weeks to view videos on different wellness topics. Control participants will have anthropometric measurements of weight, height, hip size and waist size taken at the beginning of the study, 6 weeks, and at 12 weeks. Control participants will also have a fitness test on a treadmill, full body scan, blood pressure, heart rate and questionnaires given at the beginning of the study, 6 weeks and at 12 weeks. Participants who are randomized to the 'intervention arm' will be asked to come to the study site to exercise 3 days per week for 12 weeks. The exercise duration will increase over time from 75 minutes per week to 150 minutes per week. Intervention participants will have anthropometric measurements of weight, height, hip size and waist size taken at the beginning of the study, 6 weeks, and at 12 weeks. Intervention participants will also have a fitness test on a treadmill, full body scan, blood pressure, heart rate and questionnaires given at the beginning of the study, 6 weeks and at 12 weeks. The proposed design of the intervention is to provide high does of education, support, NR, and structured exercise to optimize success experiences that can build self-doses in the first sessions. As the intervention progresses, support through mobile phones will be used to assist with problem solving and social support as participants transition to self-management. Content will be based on the extant literature on tobacco cessation, nutrition, and exercise interventions, with emphasis given to published descriptions of interventions tailored for AAW. Examples of resources from which content may be drawn include Commit to Quit, Smoke Free Woman (NCI), Pathways to Freedom (2003 version), and the Diabetes Prevention Program. Key content messages will be developed for each counseling session. all print materials will be specifically targeted with visual images and content that has been found to engage AAW. Focus groups will be conducted with women representing the targeting population in order to develop the messages and visual content. These qualitative data will be critical in the development of intervention materials that engage and connect with the women. Focus groups will be conducted during the first 3 months of the award, with the primary goal of furthering tailoring intervention materials and protocols to the lives of African-American women residing in urban District of Columbia (DC) neighborhoods. A total of 4 groups will be run with 8 women in each. The demographic makeup of the groups will resemble that of our target population on such factors as educational attainment and socio-economic status (SES). Participants will be recruited through outreach methods (flyers, community talks) used successfully by Dr. Adams-Campbell's community lab. The multiple principal investigators (MPIs) will refine the focus group facilitator's guide and review focus group transcripts and notes to maintain protocol integrity. Open-ended questions will probe views on target health behaviors as well as preferred information delivery modalities and ways to remain in contact and provide optimal support. All focus groups will be audio-taped, with a research assistant taking notes at each of the sessions. Audiotapes will then be transcribed and translated in order to analyze their content.
- * Rationale and justification for study (i.e. historical background, investigator's personal experience, pertinent medical literature, etc.): Smoking is the leading cause of preventable morbidity and mortality in the US. African Americans experience clear disparities in disease and death from smoking. African American women (AAW) are an important subgroup to study because they are distinct from non-AAW and their male African American counterparts on biopsychosocial factors that are relevant to smoking behavior. In particular, AAW have lower smoking rates compared to Caucasian women (CAW) yet similar lung cancer rates. Additional evidence indicates that AAW are more likely to develop cancer of the larynx, esophageal cancer, cerebrovascular disease, and cardiovascular disease than CAW. African American smokers are less likely to be screened by providers for tobacco use, receive advice to quit, or use cessation aids during a quit attempt, even after controlling for health service use and socioeconomic factors. Smoking cessation is the single most important preventative health behavior AAW can engage in to significantly reduce their chances of morbidity and premature mortality related to smoking related illnesses. Due to their disparate smoking-related health outcomes, targeted and tailored smoking cessation interventions are extremely critical for AAW.
Along with the disease burden of tobacco use, sedentary lifestyles and obesity pose heightened concerns for chronic diseases such as diabetes and vascular disease among AAW. In 2008, AAW had higher incidence of and mortality attributed to coronary heart disease, stroke, heart failure, and high blood pressure, as compared to non-Hispanic Whites or Hispanics. Energy balance is defined as the balance between energy taken in, generally by food and drink, and energy expanded. Lifestyle behaviors strongly linked to obesity are taken in, generally by low levels of physical activity (sedentary lifestyle) or high consumption rates of high-fat or energy-dense diets, or both. African Americans have been found to have different dietary traditions than Caucasians and to consume a higher percentage of calories from fat even after controlling for individual characteristics and neighborhood SES. Despite robust evidence of the cancer-protective and health promoting influence of physical activity (PA), more than 50% of Americans do not engage in adequate levers of PA. A recent study identified both physical inactivity and smoking as two health behaviors for which relative inequalities are increasing among those with less formal education compared with those with more. SES-related obesity disparities are also increasing in women and among African Americans. There is indeed a public health call for evidence-based research on both regionally and culturally targeted energy balance strategies that can effectively reach and engage African Americans.
Nearly all evidence-based smoking cessation programs address the importance of post-cessation weight gain through dietary choices and PA. However, these issues are not typically emphasized as centrally important to the likelihood of success of the cessation attempt. Likewise, weight control programs and initiatives that promote PA give only minimal attention to tobacco cessation. Questions remain about the most effective ways to implement interventions that simultaneously address multiple health behaviors. However, evidence continues to emerge to suggest that such interventions are not only feasible, but have advantages over approaches that focus on a single health promotion behavior. A targeted multiple health outcome intervention has promise to change health behaviors that will lead to improved health and ultimately reduce cancer death disparities among AAW. Culturally tailored comprehensive interventions that address smoking-cessation and obesity/weight-control among AAW are needed. This pilot project seeks to develop a combined health promotion intervention tailored for urban AAW smokers. "Quit \& Fit" will be designed as a 12-week program to promote smoking cessation and achieve energy balance through regular PA and healthy nutrition. The first several weeks of the intervention will provide maximum structured in-person support which will be tapered over time and followed by tailored mobile phone sessions to provide ongoing support, counseling, and assist with the transition from initial structured counseling to self-management. The program will employ evidence-based strategies that meet the needs and preferences of AAW in an urban environment.
Many studies have focused on the various health problems we aim to target, but in the other studies, these interventions have focused on only one aspect of the problem, e.g., smoking cessation alone or PA alone. The success of the proposed multiple health outcome intervention would also contribute novel findings to addressing the leading health behaviors (tobacco use, PA, diet) associated with morbidity and mortality among minority and low-income populations in this country. The opportunity to engage women at one time across multiple behaviors in a targeted and cost-effective way has significant implications. Moreover, the use of technology (cell phones) to provide support for adherence to the programs is at the cutting edge of health care delivery. Cell phones are a cost-effective way to maintain contact with, and provide support to difficult-to-engage patients. As reviewed, tailored messages delivered by phone have been found effective to change energy balance among urban African Americans. Moreover, the focus of the study on building self-efficacy through structured exercise and counseling in the initial sessions and then providing support transitioning behaviors from the structured sessions to the home environments is a unique design that can optimize retention and sustained behavior change. This program could have a profound impact on reducing tobacco-related health disparities with important implications for developing cost-efficient ways of engaging this and many other patient populations.
- Conditions
- Smoking Cessation
- Being tested
- Intervention
- Medical subject headings
- Smoking Cessation
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
InterventionOther
Participants who are randomized to the 'intervention arm' will be asked to come to the study site to exercise 3 days per week for 12 weeks. The exercise duration will increase over time from 75 minutes per week to 150 minutes per week. Intervention participants will have anthropometric measurements of weight, height, hip size and waist size taken at the beginning of the study, 6 weeks, and at 12 weeks. Intervention participants will also have a fitness test on a treadmill, full body scan, blood pressure, heart rate and questionnaires given at the beginning of the study, 6 weeks and at 12 weeks.
| Study group | Role | What they receive |
|---|---|---|
| control | Placebo comparator | Participants who are randomized to the 'control arm' will be asked to maintain their current daily activities for 12 weeks. They will also be required to visit the study site 3 times per week for 12 weeks to view videos on different wellness topics. Control participants will have anthropometric measurements of weight, height, hip size and waist size taken at the beginning of the study, 6 weeks, and at 12 weeks. Control participants will also have a fitness test on a treadmill, full body scan, blood pressure, heart rate and questionnaires given at the beginning of the study, 6 weeks and at 12 weeks. Receives: Other: Intervention |
| intervention | Experimental | Participants who are randomized to the 'intervention arm' will be asked to come to the study site to exercise 3 days per week for 12 weeks. The exercise duration will increase over time from 75 minutes per week to 150 minutes per week. Intervention participants will have anthropometric measurements of weight, height, hip size and waist size taken at the beginning of the study, 6 weeks, and at 12 weeks. Intervention participants will also have a fitness test on a treadmill, full body scan, blood pressure, heart rate and questionnaires given at the beginning of the study, 6 weeks and at 12 weeks. Receives: Other: Intervention |
What is being measured
The primary outcome is the main question the study is designed to answer.
Smoking cessation
Measured: 12 weeks
Secondary outcomes (1)
weight loss
Weight loss and/or reduce post-cessation weight gain through regular PA and healthy nutrition for AAW smoker
Measured: 12 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Apr 2014 (estimated)
- Study startApr 2013
- Primary completionNov 2017
- Study completionNov 2017
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Smoking CessationStudies of the same condition, open and under way.
- More trials run by Georgetown UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 40 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Georgetown University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Lucile Adams-Campbell, Georgetown University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02103582
- Sponsor's protocol ID
- 2012-1516 Georgetown Lombardi
- Acronym
- Quit and Fit
- Status last verified
- Nov 2017
- First submitted
- 27 Mar 2014
- Last updated
- 29 Nov 2017
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 29 Nov 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Quit and Fit: A Tobacco Cessation and Energy Balance Pilot for African Americans
- ClinicalTrials.gov ID
- NCT02103582
- Acronym / sponsor ID
- Quit and Fit / 2012-1516 Georgetown Lombardi
- Conditions
- Smoking Cessation
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 40 participants (estimated)
- Lead sponsor
- Georgetown UniversityUniversity, hospital or other
- Study start
- Apr 2013
- Primary completion
- Nov 2017 (actual)
- Study completion
- Nov 2017 (actual)
- First posted
- 4 Apr 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The Quit \& Fit intervention will be designed as a 12-week study to promote smoking cessation, increase physical activity levels, and reduce weight gain through regular exercise and healthy nutrition for African American Women smokers.
Patients will be assigned to the fitness intervention group or control groups by a computer.
Detailed description
- * Purpose of project (one or two sentences): The feasibility phase of the proposed study is comprised of a two-arm randomized pilot trial to evaluate the feasibility, satisfaction, and preliminary efficacy of 'Quit \& Fit'. Women (N=40) will receive 12 weekly smoking cessation telephone counseling sessions. Participants will be randomized to either a fitness intervention (Quit \& Fit) or a contact time control (Quit for Life).
- * Study design (for example, hypothesis, research questions, standard and experimental procedures/drugs/devices or equipment, etc.): The Quit \& Fit intervention will be designed as a 12-week, tailored multiple health outcome intervention to promote smoking cessation, achieve energy balance, and reduce post-cessation weight gain through regular PA and healthy nutrition for AAW smokers. Culturally tailored comprehensive interventions that address smoking-cessation and obesity/weight-control among AAW are needed. The conceptual basis of the proposal is Albert Bandura's social cognitive Theory (SCT), which posits that people learn through observation and modeling of behaviors, attitudes, and emotional reactions. When applied to smoking cessation and health behavior change, social learning can be viewed as a transition through stages of increased knowledge, self-efficacy, and social support, culminating in readiness to change behaviors. The SCT model allows for targeting of factors relevant to a given individual and tailoring messages to each each participant's cultural values. Participants will be randomized into one of the study groups: the 'control arm' or the 'exercise arm'. Both groups will receive 12 weeks of smoking cessation counseling, telephone counseling and and will receive 10 weeks of nicotine replacement therapy (NRT) in the form of nicotine lozenges. Participants who are randomized to the 'control arm' will be asked to maintain their current daily activities for 12 weeks. They will also be required to visit the study site 3 times per week for 12 weeks to view videos on different wellness topics. Control participants will have anthropometric measurements of weight, height, hip size and waist size taken at the beginning of the study, 6 weeks, and at 12 weeks. Control participants will also have a fitness test on a treadmill, full body scan, blood pressure, heart rate and questionnaires given at the beginning of the study, 6 weeks and at 12 weeks. Participants who are randomized to the 'intervention arm' will be asked to come to the study site to exercise 3 days per week for 12 weeks. The exercise duration will increase over time from 75 minutes per week to 150 minutes per week. Intervention participants will have anthropometric measurements of weight, height, hip size and waist size taken at the beginning of the study, 6 weeks, and at 12 weeks. Intervention participants will also have a fitness test on a treadmill, full body scan, blood pressure, heart rate and questionnaires given at the beginning of the study, 6 weeks and at 12 weeks. The proposed design of the intervention is to provide high does of education, support, NR, and structured exercise to optimize success experiences that can build self-doses in the first sessions. As the intervention progresses, support through mobile phones will be used to assist with problem solving and social support as participants transition to self-management. Content will be based on the extant literature on tobacco cessation, nutrition, and exercise interventions, with emphasis given to published descriptions of interventions tailored for AAW. Examples of resources from which content may be drawn include Commit to Quit, Smoke Free Woman (NCI), Pathways to Freedom (2003 version), and the Diabetes Prevention Program. Key content messages will be developed for each counseling session. all print materials will be specifically targeted with visual images and content that has been found to engage AAW. Focus groups will be conducted with women representing the targeting population in order to develop the messages and visual content. These qualitative data will be critical in the development of intervention materials that engage and connect with the women. Focus groups will be conducted during the first 3 months of the award, with the primary goal of furthering tailoring intervention materials and protocols to the lives of African-American women residing in urban District of Columbia (DC) neighborhoods. A total of 4 groups will be run with 8 women in each. The demographic makeup of the groups will resemble that of our target population on such factors as educational attainment and socio-economic status (SES). Participants will be recruited through outreach methods (flyers, community talks) used successfully by Dr. Adams-Campbell's community lab. The multiple principal investigators (MPIs) will refine the focus group facilitator's guide and review focus group transcripts and notes to maintain protocol integrity. Open-ended questions will probe views on target health behaviors as well as preferred information delivery modalities and ways to remain in contact and provide optimal support. All focus groups will be audio-taped, with a research assistant taking notes at each of the sessions. Audiotapes will then be transcribed and translated in order to analyze their content.
- * Rationale and justification for study (i.e. historical background, investigator's personal experience, pertinent medical literature, etc.): Smoking is the leading cause of preventable morbidity and mortality in the US. African Americans experience clear disparities in disease and death from smoking. African American women (AAW) are an important subgroup to study because they are distinct from non-AAW and their male African American counterparts on biopsychosocial factors that are relevant to smoking behavior. In particular, AAW have lower smoking rates compared to Caucasian women (CAW) yet similar lung cancer rates. Additional evidence indicates that AAW are more likely to develop cancer of the larynx, esophageal cancer, cerebrovascular disease, and cardiovascular disease than CAW. African American smokers are less likely to be screened by providers for tobacco use, receive advice to quit, or use cessation aids during a quit attempt, even after controlling for health service use and socioeconomic factors. Smoking cessation is the single most important preventative health behavior AAW can engage in to significantly reduce their chances of morbidity and premature mortality related to smoking related illnesses. Due to their disparate smoking-related health outcomes, targeted and tailored smoking cessation interventions are extremely critical for AAW.
Along with the disease burden of tobacco use, sedentary lifestyles and obesity pose heightened concerns for chronic diseases such as diabetes and vascular disease among AAW. In 2008, AAW had higher incidence of and mortality attributed to coronary heart disease, stroke, heart failure, and high blood pressure, as compared to non-Hispanic Whites or Hispanics. Energy balance is defined as the balance between energy taken in, generally by food and drink, and energy expanded. Lifestyle behaviors strongly linked to obesity are taken in, generally by low levels of physical activity (sedentary lifestyle) or high consumption rates of high-fat or energy-dense diets, or both. African Americans have been found to have different dietary traditions than Caucasians and to consume a higher percentage of calories from fat even after controlling for individual characteristics and neighborhood SES. Despite robust evidence of the cancer-protective and health promoting influence of physical activity (PA), more than 50% of Americans do not engage in adequate levers of PA. A recent study identified both physical inactivity and smoking as two health behaviors for which relative inequalities are increasing among those with less formal education compared with those with more. SES-related obesity disparities are also increasing in women and among African Americans. There is indeed a public health call for evidence-based research on both regionally and culturally targeted energy balance strategies that can effectively reach and engage African Americans.
Nearly all evidence-based smoking cessation programs address the importance of post-cessation weight gain through dietary choices and PA. However, these issues are not typically emphasized as centrally important to the likelihood of success of the cessation attempt. Likewise, weight control programs and initiatives that promote PA give only minimal attention to tobacco cessation. Questions remain about the most effective ways to implement interventions that simultaneously address multiple health behaviors. However, evidence continues to emerge to suggest that such interventions are not only feasible, but have advantages over approaches that focus on a single health promotion behavior. A targeted multiple health outcome intervention has promise to change health behaviors that will lead to improved health and ultimately reduce cancer death disparities among AAW. Culturally tailored comprehensive interventions that address smoking-cessation and obesity/weight-control among AAW are needed. This pilot project seeks to develop a combined health promotion intervention tailored for urban AAW smokers. "Quit \& Fit" will be designed as a 12-week program to promote smoking cessation and achieve energy balance through regular PA and healthy nutrition. The first several weeks of the intervention will provide maximum structured in-person support which will be tapered over time and followed by tailored mobile phone sessions to provide ongoing support, counseling, and assist with the transition from initial structured counseling to self-management. The program will employ evidence-based strategies that meet the needs and preferences of AAW in an urban environment.
Many studies have focused on the various health problems we aim to target, but in the other studies, these interventions have focused on only one aspect of the problem, e.g., smoking cessation alone or PA alone. The success of the proposed multiple health outcome intervention would also contribute novel findings to addressing the leading health behaviors (tobacco use, PA, diet) associated with morbidity and mortality among minority and low-income populations in this country. The opportunity to engage women at one time across multiple behaviors in a targeted and cost-effective way has significant implications. Moreover, the use of technology (cell phones) to provide support for adherence to the programs is at the cutting edge of health care delivery. Cell phones are a cost-effective way to maintain contact with, and provide support to difficult-to-engage patients. As reviewed, tailored messages delivered by phone have been found effective to change energy balance among urban African Americans. Moreover, the focus of the study on building self-efficacy through structured exercise and counseling in the initial sessions and then providing support transitioning behaviors from the structured sessions to the home environments is a unique design that can optimize retention and sustained behavior change. This program could have a profound impact on reducing tobacco-related health disparities with important implications for developing cost-efficient ways of engaging this and many other patient populations.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| control | Placebo comparator | Other: InterventionParticipants who are randomized to the 'control arm' will be asked to maintain their current daily activities for 12 weeks. They will also be required to visit the study site 3 times per week for 12 weeks to view videos on different wellness topics. Control participants will have anthropometric measurements of weight, height, hip size and waist size taken at the beginning of the study, 6 weeks, and at 12 weeks. Control participants will also have a fitness test on a treadmill, full body scan, blood pressure, heart rate and questionnaires given at the beginning of the study, 6 weeks and at 12 weeks. |
| intervention | Experimental | Other: InterventionParticipants who are randomized to the 'intervention arm' will be asked to come to the study site to exercise 3 days per week for 12 weeks. The exercise duration will increase over time from 75 minutes per week to 150 minutes per week. Intervention participants will have anthropometric measurements of weight, height, hip size and waist size taken at the beginning of the study, 6 weeks, and at 12 weeks. Intervention participants will also have a fitness test on a treadmill, full body scan, blood pressure, heart rate and questionnaires given at the beginning of the study, 6 weeks and at 12 weeks. |
Who may qualify
- Ages
- 18 to 69 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- African American women ages 18-69;
- Currently smoke at least 5 cigarettes per day;
- Smoked daily for the past one year;
- Able to provide informed consent;
- Generally good health as determined by medical history;
Key exclusion criteria (5 listed)
- Women who are:
- Currently pregnant; or have
- heart disease,
- lung disease, or
- mental illness
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| InterventionParticipants who are randomized to the 'intervention arm' will be asked to come to the study site to exercise 3 days per week for 12 weeks. The exercise duration will increase over time from 75 minutes per week to 150 minutes per week. Intervention participants will have anthropometric measurements of weight, height, hip size and waist size taken at the beginning of the study, 6 weeks, and at 12 weeks. Intervention participants will also have a fitness test on a treadmill, full body scan, blood pressure, heart rate and questionnaires given at the beginning of the study, 6 weeks and at 12 weeks. | Other | control, intervention |
Primary outcome
Smoking cessation
Time frame: 12 weeks
1 secondary outcome
weight loss
Time frame: 12 weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Nov 2017.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Intervention in people with Smoking Cessation, run by Georgetown University at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 29 Nov 2017. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Smoking cessation (time frame: 12 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Nov 2017.