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Community Based Tobacco Cessation Programme Mumbai

Community Based Tobacco Cessation Programme

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01958255
Acronym
CBTCP
Enrollment
279
Registered
2013-10-09
Start date
2012-05-31
Completion date
2014-04-30
Last updated
2018-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tobacco Smoking Behavior

Keywords

tobacco quit rates

Brief summary

The aim of this project was to provide tobacco cessation services to the women at the community level at their door steps and thus establish a model community based tobacco cessation programme which could be replicated in other communities and could be taken up by National Tobacco Control Programme (NTCP), in future.

Detailed description

The study was extended over a period of one year. There were 3 interventions given at the interval of 3 months each. The post intervention questionnaire regarding knowledge, attitude and practices was planned filled at the end of the programme i.e. 9th to 12th month from start of the programme. A community based tobacco cessation programme, which has the potential of being first of its kind, for women, was planned by the department of Preventive Oncology for the women in a geographical community in and around Mankhurd in Mumbai,for providing tobacco cessation counseling services. Doorstep services were provided to these women as they were unlikely to avail the tobacco cessation services at the clinic in TMH since their priority is managing household chores and caretaking of their family. The selected community was a part of women cancer screening programme namely; Tata Memorial Hospital Mobile Outreach Programme (TMH-MOP). The women who were current tobacco users at the time of screening under TMH-MOP were enrolled for this study.The women were intervened thrice at an interval of 3 months each and tobacco cessation counseling was provided at each intervention. The post intervention data was collected at the end of all the 3 counseling sessions. Sessions were held for rapport building with the participant women. Questionnaire were filled to record the information on the details of different forms of tobacco usage, factors responsible for initiation and continuation of tobacco use, pre-intervention and post-intervention knowledge, attitudes and practices regarding tobacco habits and severity of tobacco use (Fagerstroms scale). This programme was aimed at creating awareness and educating women regarding the health hazards of tobacco use, at the community level, at their door step.

Interventions

BEHAVIORALplanned intervention for tobacco cessation counseling

game session for rapport building followed by group discussion and tobacco cessation counseling

Sponsors

Tata Memorial Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

all current tobacco users at the time of screening under TMH-MOP project

Exclusion criteria

All those who refused to participate and those who could not be contacted during the study period

Design outcomes

Primary

MeasureTime frameDescription
To assess tobacco quit ratesBaseline and 12 monthsThe participant women were intervened thrice for counseling about quitting tobacco and quit rates were assessed at the end of one year

Secondary

MeasureTime frameDescription
To assess pre-intervention knowledge, attitude and practices about tobacco use.baselineA questionnaire to assess the baseline knowledge, attitude and practices about tobacco use by participant women was filled during first intervention
To assess post-intervention knowledge, attitude and practices of tobacco use by participant women.9 month and 12 monthA questionnaire to assess the baseline knowledge, attitude and practices about tobacco use by participant women was filled during post intervention

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026