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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.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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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
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.

Sharmila A Pimple, Professor contact

+912224154379

drsharmilapatil@yahoo.com

Gauravi A Mishra, Assoc Prof contact

+912224177000 ext. 4634

gauravi2005@yahoo.co.in

India1 site, 1 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

    Recruiting

Other trials in India

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:

  1. To assess knowledge and understand the practices related to tobacco use among the Zari workers' population using qualitative research.
  2. To implement a multicomponent community-based intervention model through trained health workers in an unorganized workplace setting.
  3. To assess any change in the Knowledge Attitude and Practices related to tobacco use at post intervention.
  4. Determine tobacco cessation rates at the end of intervention.

Secondary Objectives:

  1. To provide oral screening service to the target groups at the end of the interventions.
  2. 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 :

  1. 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.
  2. 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.
  3. 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

  1. Medium Intensity Intervention The Medium intensity arm will implement the multi-component program with three contact programs.
  2. First Contact program: Group health education session II. Second Contact program: Focus Group Discussion III. Third Contact program: Brief Individual Counseling session
  3. 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.

  1. 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.
  2. 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.

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 groups in NCT02103868
Study groupRoleWhat they receive
ControlNo interventionNo active intervention will be given for tobacco cessation.
Medium InterventionExperimentalTobacco Cessation Counseling : Medium intervention in the form of 3 contact sessions will be given for tobacco cessation.
Receives: Behavioral: Tobacco Cessation Counseling
Low intensity interventionExperimentalTobacco 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.

  1. 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.

  1. First posted4 Apr 2014 (estimated)
  2. Study startOct 2013
  3. Primary completionJan 2016 (estimated)
  4. Study completionJan 2016 (estimated)

Resources

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)
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

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.

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