Tobacco CessationZARINCT02103868
Medium Vs Low Intensity Intervention in Tobacco Cessation and Control in Zari Workers
A study testing Tobacco Cessation Counseling in people with Tobacco Cessation, run by Tata Memorial Hospital at 1 site in India.
Trial summary
Zari workers in Mumbai city will be assessed for tobacco consumption habit. They will be divided into 3 arms as - 1) First arm will get Medium intensity tobacco cessation intervention 2) Second arm will get low intensity tobacco cessation intervention 3) Control arm. Read more about this study
- Who is it for?
- Ages 15 to 90 years
- Conditions the study is for
- Tobacco Cessation
- What is being tested?
- Tobacco Cessation Counseling
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 400 participants
- Where
- 1 siteIndia
- Study dates
- Oct 2013to Jan 2016
- 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 15 to 90 years
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- Subjects who are willing to participate
- All workers employed in each of the listed zari units.
- Who are willing to give informed consent.
Who cannot join
- 1. Who are NOT willing to give informed consent.
Trial locations and contacts
1 site in 1 country.
India1 site, 1 recruiting
- Recruiting
Tata Memorial Hospital
Mumbai, Maharashtra, 400012
Sharmila A Pimple, Professor, +912224154379, drsharmilapatil@yahoo.com
Gauravi A Mishra, Assoc Prof, +912224177000 ext. 4634, gauravi2005@yahoo.co.in
About this study
Official title: Interventional Study to Determine the Effectiveness of Medium Intensity Verses Low Intensity Tobacco Use Prevention and Cessation Intervention in the Unorganized Sector of Zari Workers in Mumbai
Zari workers in Mumbai city will be assessed for tobacco consumption habit. They will be divided into 3 arms as - 1) First arm will get Medium intensity tobacco cessation intervention 2) Second arm will get low intensity tobacco cessation intervention 3) Control arm. At the end of 12 months of intervention quit rates will be compared.
Read the detailed description
Aims and Objectives
Broad objective:
The proposed study is planned to understand prevalence and practices related to tobacco use among workers of the informal sector of Zari Industry and to assess the feasibility and acceptability of effective strategies of a programmatic approach towards tobacco use prevention and cessation intervention model in this by assessment of pre and post-intervention knowledge, attitude and perception of tobacco use, followed by offering education and cessation and finally assessing the impact and outcomes by changes in the attitudes towards tobacco use and quit rates among tobacco users.
Specific objectives:
Primary Objectives:
- To assess knowledge and understand the practices related to tobacco use among the Zari workers' population using qualitative research.
- To implement a multicomponent community-based intervention model through trained health workers in an unorganized workplace setting.
- To assess any change in the Knowledge Attitude and Practices related to tobacco use at post intervention.
- Determine tobacco cessation rates at the end of intervention.
Secondary Objectives:
- To provide oral screening service to the target groups at the end of the interventions.
- Develop a LOCAL -language tobacco use prevention and cessation training module to train counsellors in tobacco cessation interventions.
Study Methodology
Design:
A prospective, community-based randomized controlled design
Settings: Community based Zari work units of three urban slum pockets in Mumbai
Sampling:
Three distinct urban slum communities in Mumbai where Zari units operate will be identified. Each of the slum community will serve as three arms of the trial, with one geographic cluster / community serving as the intervention community for moderate intensity intervention, second cluster /community for low intensity intervention and the third cluster/community serving as the control arm with no intervention. These communities will be recruited on the basis of comparable socio-demographic characteristics.
Tools of Data Collection:
Questionnaire:
A pre designed structured baseline questionnaire will be prepared to understand the determinants that trigger the onset of tobacco use, dynamics of regular use of tobacco and factors that motivate the user to quit tobacco. Written informed consent will be taken from all the participants.
The questionnaire at baseline will be administered in local language before the implementation of the intervention and will be repeated after 1 year with the same sample at end to assess the efficacy of the intervention. The questionnaire will be administered by a trained interviewer as per the convenience of the respondents.
Intervention Arm:
Intervention A community-based multi-component intervention model developed, will be implemented and evaluated in the intervention community. The intervention model will address numerous socio-environmental and intra-personal factors that trigger the onset of tobacco use and other determinants that influence tobacco cessation.
The intervention consists of :
- Awareness \& Education on Tobacco use prevention: Interactive activities, pre-tested posters, in addition, pictorial handouts, booklets and pamphlets will be distributed for knowledge enhancement by trained social workers. The first interaction with the workers will involve an elaborate common education programme on harms of tobacco use, tobacco use prevention and benefits of tobacco cessation, by an audio visual presentation and distribution of pamphlets for knowledge enhancement by trained social workers. All participants will be assessed for their tobacco use status prior to the intervention. The participants with history of current tobacco use in any form will then be enrolled for further interventions for tobacco cessation. A structured questionnaire detailing information on sociodemographic variables with medical and other risk factors with complete assessment of their tobacco habit will be entered by medical social workers. All participants will be assessed for their tobacco use status at all interventions.
- Focus Group discussion: This tobacco cessation intervention session with the tobacco users after three months of the first contact program will involve thirty minutes of focus group discussion with group behavioral therapy in groups of 5-10 individuals for reinforcement of tobacco use prevention and cessation advice. Group discussion is intended to improve understanding by exploring, sharing and reflecting psychosocial, familial, environmental issues which attribute to the problem. Members of the group are encouraged to exchange information and ideas about the perceived barriers towards tobacco cessation. Techniques like reflecting, exploring and re-evaluation will be used to identify their problem to improve insight and reinforce attitudinal change.
- Individual tobacco cessation counseling sessions:
Iindividual counseling is commonly used to help people who are trying to quit tobacco. The counseling adopting a interactive problem-solving approach will be done by trained Medical Social Workers providing face-to-face sessions for 10-15 minutes per participant,
Types of Intervention
- Medium Intensity Intervention The Medium intensity arm will implement the multi-component program with three contact programs.
- First Contact program: Group health education session II. Second Contact program: Focus Group Discussion III. Third Contact program: Brief Individual Counseling session
- Low Intensity Intervention
Single contact session with Group health education session will be provided to the participants
Final Outcome Final outcome measure, the quit rates as self reported tobacco abstinence will be assessed at the end of one year.
Oral cancer screening:
All the Zari workers will also be invited for oral cancer screening at the end of intervention program.
Oral cancer screening to detect clinically recognizable precancerous lesions (leukoplakia, erythroplakia and oral submucous fibrosis) and asymptomatic early invasive lesions will be done by trained Primary Health Workers. Visual examination of the oral cavity with good light source like halogen flashlight, is a simple approach to detect asymptomatic oral cancers and precancerous lesions. The performance characteristics of this test are satisfactory in terms of sensitivity, specificity, and predictive value therefore, it is a suitable screening test for oral cancer. One large study from Kerala has shown that screening by visual inspection of the mouth by trained health workers may potentially reduce mortality in high risk groups.
The clinical findings will be recorded as 1. Normal; 2. Benign or non cancerous lesions such as fissures in the tongue, aphthous ulcer, black patch, tobacco-related blanching, fibroma, hypertrophied papillae, etc.; and 3. Pre cancer lesions if found to have a white patch, ulcerated white patch, verrucous lesion, submucous fibrosis, red patch, suspicious ulcer or growth. All the above findings suspicious for oral precancer on screening evaluation will be referred for further diagnostic evaluation by medical officers.
Control Arm:
No Active Intervention will be given in the control arm, but will distributed tobacco awareness pamphlets in local languages. Only base line and end line survey assessment will be done.
Training as tobacco cessation counselors \& Development of Module.
- Recruitment and training of staff This involves the recruitment of project personnel and their training. Training would involve the theoretical and practical teaching of questionnaire/survey as well modular training for tobacco cessation counseling to the project personnel.
- Preparation of resource materials and questionnaire formats Resource materials would include training module for tobacco use prevention and tobacco cessation techniques with Individual and Group therapy sessions with pamphlets outlining the harmful effects of tobacco.
Outcome measures
The two outcome measures used from the survey questionnaire were 'ever use' and 'current use' of tobacco at baseline and endline. 'Ever users' were those who had consumed tobacco in any form in their life time. 'Current users' were those who had consumed tobacco in any form in the past one week. Current use at baseline and endline were compared to calculate the 'quit rate' and 'rate of fresh uptake'. Quit rate of tobacco use among the communities will be estimated as the proportion of workers who become non-users at endline from among those who were current users in the baseline survey. Rate of fresh uptake will be estimated as the proportion of workers who reported themselves as ever users or current users at endline from among those who were never users at the baseline survey.
Data Management and Analysis
Data will be entered and analyzed using SPSS version 18.3 The trial data will be analyzed on an intention to treat basis and the participants will be included in the final analysis irrespective of whether or not they could be followed up in all subsequent visits. Self reported history will be taken as the main criteria to assess outcome of tobacco cessation. Multivariate analysis will be performed to identify the factors promoting the use of tobacco and quitting tobacco. The tobacco quit rates will be calculated as percentages. The post intervention changes in the KAP of employees will be compared to the pre-intervention KAP. Groups will be compared using non-parametric statistical techniques.
- Conditions
- Tobacco Cessation
- Being tested
- Tobacco Cessation Counseling
- Keywords
- Tobacco cessation, Zari worker, Behavior therapy, Qualitative Research, Mumbai
- Medical subject headings
- Tobacco Use Cessation
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Tobacco Cessation CounselingBehavioural
Also called TCC
Doing group and personal counseling for tobacco cessation
| Study group | Role | What they receive |
|---|---|---|
| Control | No intervention | No active intervention will be given for tobacco cessation. |
| Medium Intervention | Experimental | Tobacco Cessation Counseling : Medium intervention in the form of 3 contact sessions will be given for tobacco cessation. Receives: Behavioral: Tobacco Cessation Counseling |
| Low intensity intervention | Experimental | Tobacco Cessation Counseling: Only a single contact session will be done for tobacco cessation. Receives: Behavioral: Tobacco Cessation Counseling |
What is being measured
The primary outcome is the main question the study is designed to answer.
Tobacco Quit Rate
Tobacco quit rates in moderate intensity behavioural intervention, low intensity behavioral intervention and control group will be compared at the end of 12 months
Measured: 12 Months
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 startOct 2013
- Primary completionJan 2016 (estimated)
- Study completionJan 2016 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Tobacco CessationStudies of the same condition, open and under way.
- 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
- Health services research
- Allocation
- Randomised
- Intervention model
- Factorial
- Masking
- None (open label)
- Enrolment
- 400 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Tata Memorial Hospital
- Sponsor type
- Other government
- Responsible party
- Principal investigator, Dr Sharmila Pimple, Tata Memorial Hospital
- Investigators
- Sharmila A Pimple, Professor, Principal investigator, Tata Memorial HospitalGauravi A Mishra, Assoc Prof, Principal investigator, Tata Memorial HospitalParishi Majmudar, MSW, Principal investigator, Tata Memorial Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02103868
- Sponsor's protocol ID
- TMHPOZariW2013
- Acronym
- ZARI
- Status last verified
- Feb 2015
- First submitted
- 1 Apr 2014
- Last updated
- 5 Feb 2015
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 5 Feb 2015. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Interventional Study to Determine the Effectiveness of Medium Intensity Verses Low Intensity Tobacco Use Prevention and Cessation Intervention in the Unorganized Sector of Zari Workers in Mumbai
- ClinicalTrials.gov ID
- NCT02103868
- Acronym / sponsor ID
- ZARI / TMHPOZariW2013
- Conditions
- Tobacco Cessation
- Keywords
- Tobacco cessation, Zari worker, Behavior therapy, Qualitative Research, Mumbai
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 400 participants (estimated)
- Lead sponsor
- Tata Memorial HospitalOther government
- Study start
- Oct 2013
- Primary completion
- Jan 2016 (estimated)
- Study completion
- Jan 2016 (estimated)
- 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.
Zari workers in Mumbai city will be assessed for tobacco consumption habit. They will be divided into 3 arms as - 1) First arm will get Medium intensity tobacco cessation intervention 2) Second arm will get low intensity tobacco cessation intervention 3) Control arm. At the end of 12 months of intervention quit rates will be compared.
Detailed description
Aims and Objectives
Broad objective:
The proposed study is planned to understand prevalence and practices related to tobacco use among workers of the informal sector of Zari Industry and to assess the feasibility and acceptability of effective strategies of a programmatic approach towards tobacco use prevention and cessation intervention model in this by assessment of pre and post-intervention knowledge, attitude and perception of tobacco use, followed by offering education and cessation and finally assessing the impact and outcomes by changes in the attitudes towards tobacco use and quit rates among tobacco users.
Specific objectives:
Primary Objectives:
- To assess knowledge and understand the practices related to tobacco use among the Zari workers' population using qualitative research.
- To implement a multicomponent community-based intervention model through trained health workers in an unorganized workplace setting.
- To assess any change in the Knowledge Attitude and Practices related to tobacco use at post intervention.
- Determine tobacco cessation rates at the end of intervention.
Secondary Objectives:
- To provide oral screening service to the target groups at the end of the interventions.
- Develop a LOCAL -language tobacco use prevention and cessation training module to train counsellors in tobacco cessation interventions.
Study Methodology
Design:
A prospective, community-based randomized controlled design
Settings: Community based Zari work units of three urban slum pockets in Mumbai
Sampling:
Three distinct urban slum communities in Mumbai where Zari units operate will be identified. Each of the slum community will serve as three arms of the trial, with one geographic cluster / community serving as the intervention community for moderate intensity intervention, second cluster /community for low intensity intervention and the third cluster/community serving as the control arm with no intervention. These communities will be recruited on the basis of comparable socio-demographic characteristics.
Tools of Data Collection:
Questionnaire:
A pre designed structured baseline questionnaire will be prepared to understand the determinants that trigger the onset of tobacco use, dynamics of regular use of tobacco and factors that motivate the user to quit tobacco. Written informed consent will be taken from all the participants.
The questionnaire at baseline will be administered in local language before the implementation of the intervention and will be repeated after 1 year with the same sample at end to assess the efficacy of the intervention. The questionnaire will be administered by a trained interviewer as per the convenience of the respondents.
Intervention Arm:
Intervention A community-based multi-component intervention model developed, will be implemented and evaluated in the intervention community. The intervention model will address numerous socio-environmental and intra-personal factors that trigger the onset of tobacco use and other determinants that influence tobacco cessation.
The intervention consists of :
- Awareness \& Education on Tobacco use prevention: Interactive activities, pre-tested posters, in addition, pictorial handouts, booklets and pamphlets will be distributed for knowledge enhancement by trained social workers. The first interaction with the workers will involve an elaborate common education programme on harms of tobacco use, tobacco use prevention and benefits of tobacco cessation, by an audio visual presentation and distribution of pamphlets for knowledge enhancement by trained social workers. All participants will be assessed for their tobacco use status prior to the intervention. The participants with history of current tobacco use in any form will then be enrolled for further interventions for tobacco cessation. A structured questionnaire detailing information on sociodemographic variables with medical and other risk factors with complete assessment of their tobacco habit will be entered by medical social workers. All participants will be assessed for their tobacco use status at all interventions.
- Focus Group discussion: This tobacco cessation intervention session with the tobacco users after three months of the first contact program will involve thirty minutes of focus group discussion with group behavioral therapy in groups of 5-10 individuals for reinforcement of tobacco use prevention and cessation advice. Group discussion is intended to improve understanding by exploring, sharing and reflecting psychosocial, familial, environmental issues which attribute to the problem. Members of the group are encouraged to exchange information and ideas about the perceived barriers towards tobacco cessation. Techniques like reflecting, exploring and re-evaluation will be used to identify their problem to improve insight and reinforce attitudinal change.
- Individual tobacco cessation counseling sessions:
Iindividual counseling is commonly used to help people who are trying to quit tobacco. The counseling adopting a interactive problem-solving approach will be done by trained Medical Social Workers providing face-to-face sessions for 10-15 minutes per participant,
Types of Intervention
- Medium Intensity Intervention The Medium intensity arm will implement the multi-component program with three contact programs.
- First Contact program: Group health education session II. Second Contact program: Focus Group Discussion III. Third Contact program: Brief Individual Counseling session
- Low Intensity Intervention
Single contact session with Group health education session will be provided to the participants
Final Outcome Final outcome measure, the quit rates as self reported tobacco abstinence will be assessed at the end of one year.
Oral cancer screening:
All the Zari workers will also be invited for oral cancer screening at the end of intervention program.
Oral cancer screening to detect clinically recognizable precancerous lesions (leukoplakia, erythroplakia and oral submucous fibrosis) and asymptomatic early invasive lesions will be done by trained Primary Health Workers. Visual examination of the oral cavity with good light source like halogen flashlight, is a simple approach to detect asymptomatic oral cancers and precancerous lesions. The performance characteristics of this test are satisfactory in terms of sensitivity, specificity, and predictive value therefore, it is a suitable screening test for oral cancer. One large study from Kerala has shown that screening by visual inspection of the mouth by trained health workers may potentially reduce mortality in high risk groups.
The clinical findings will be recorded as 1. Normal; 2. Benign or non cancerous lesions such as fissures in the tongue, aphthous ulcer, black patch, tobacco-related blanching, fibroma, hypertrophied papillae, etc.; and 3. Pre cancer lesions if found to have a white patch, ulcerated white patch, verrucous lesion, submucous fibrosis, red patch, suspicious ulcer or growth. All the above findings suspicious for oral precancer on screening evaluation will be referred for further diagnostic evaluation by medical officers.
Control Arm:
No Active Intervention will be given in the control arm, but will distributed tobacco awareness pamphlets in local languages. Only base line and end line survey assessment will be done.
Training as tobacco cessation counselors \& Development of Module.
- Recruitment and training of staff This involves the recruitment of project personnel and their training. Training would involve the theoretical and practical teaching of questionnaire/survey as well modular training for tobacco cessation counseling to the project personnel.
- Preparation of resource materials and questionnaire formats Resource materials would include training module for tobacco use prevention and tobacco cessation techniques with Individual and Group therapy sessions with pamphlets outlining the harmful effects of tobacco.
Outcome measures
The two outcome measures used from the survey questionnaire were 'ever use' and 'current use' of tobacco at baseline and endline. 'Ever users' were those who had consumed tobacco in any form in their life time. 'Current users' were those who had consumed tobacco in any form in the past one week. Current use at baseline and endline were compared to calculate the 'quit rate' and 'rate of fresh uptake'. Quit rate of tobacco use among the communities will be estimated as the proportion of workers who become non-users at endline from among those who were current users in the baseline survey. Rate of fresh uptake will be estimated as the proportion of workers who reported themselves as ever users or current users at endline from among those who were never users at the baseline survey.
Data Management and Analysis
Data will be entered and analyzed using SPSS version 18.3 The trial data will be analyzed on an intention to treat basis and the participants will be included in the final analysis irrespective of whether or not they could be followed up in all subsequent visits. Self reported history will be taken as the main criteria to assess outcome of tobacco cessation. Multivariate analysis will be performed to identify the factors promoting the use of tobacco and quitting tobacco. The tobacco quit rates will be calculated as percentages. The post intervention changes in the KAP of employees will be compared to the pre-intervention KAP. Groups will be compared using non-parametric statistical techniques.
Study design
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Factorial
- Masking
- None (open label)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Control | No intervention | –No active intervention will be given for tobacco cessation. |
| Medium Intervention | Experimental | Behavioral: Tobacco Cessation CounselingTobacco Cessation Counseling : Medium intervention in the form of 3 contact sessions will be given for tobacco cessation. |
| Low intensity intervention | Experimental | Behavioral: Tobacco Cessation CounselingTobacco Cessation Counseling: Only a single contact session will be done for tobacco cessation. |
Who may qualify
- Ages
- 15 to 90 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (3 listed)
- Subjects who are willing to participate
- All workers employed in each of the listed zari units.
- Who are willing to give informed consent.
Key exclusion criteria (1 listed)
- 1. Who are NOT willing to give informed consent.
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 |
|---|---|---|
| Tobacco Cessation CounselingAlso: TCCDoing group and personal counseling for tobacco cessation | Behavioural | Low intensity intervention, Medium Intervention |
Primary outcome
Tobacco Quit Rate
Time frame: 12 Months
Tobacco quit rates in moderate intensity behavioural intervention, low intensity behavioral intervention and control group will be compared at the end of 12 months
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Feb 2015.
- Tata Memorial Centre, Mumbai Official websiteLink provided by the sponsor.
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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.
Sharmila A Pimple, Professor principal investigator
Tata Memorial Hospital
Gauravi A Mishra, Assoc Prof principal investigator
Tata Memorial Hospital
Parishi Majmudar, MSW principal investigator
Tata Memorial Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Tobacco Cessation Counseling in people with Tobacco Cessation, run by Tata Memorial Hospital at 1 site in India.
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 3 inclusion and 1 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: status not confirmed, as of the sponsor's last update on 5 Feb 2015. 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 India. 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. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Sharmila A Pimple, Professor (+912224154379, drsharmilapatil@yahoo.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Tobacco Quit Rate (time frame: 12 Months). 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 5 Feb 2015.