A quasi-experimental intervention to assess the effectiveness of a physician-delivered tobacco cessation intervention in India: A detailed study protocol

Introduction: Tobacco cessation is the most important, cost-effective preventive maintenance that clinicians can offer study participants who use tobacco. There is lack of preparedness among primary care physicians in delivering cessation interventions. There are also limited studies which record th...

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Main Authors: Rajmohan Panda, Sandeep Mahapatra, Kumar Gaurav, Sanghamitra Pati, Manu Raj Mathur
Format: Article
Language:English
Published: SAGE Publishing 2017-03-01
Series:SAGE Open Medicine
Online Access:https://doi.org/10.1177/2050312117697173
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spelling doaj-7cb5bb32c13046d5907827fcbb2827b42020-11-25T03:24:45ZengSAGE PublishingSAGE Open Medicine2050-31212017-03-01510.1177/205031211769717310.1177_2050312117697173A quasi-experimental intervention to assess the effectiveness of a physician-delivered tobacco cessation intervention in India: A detailed study protocolRajmohan Panda0Sandeep Mahapatra1Kumar Gaurav2Sanghamitra Pati3Manu Raj Mathur4Public Health Foundation of India, Gurgaon, IndiaIndian Institute of Public Health, Bhubaneswar, IndiaPublic Health Foundation of India, Gurgaon, IndiaRegional Medical Research Centre (RMRC), Bhubaneswar, IndiaPublic Health Foundation of India, Gurgaon, IndiaIntroduction: Tobacco cessation is the most important, cost-effective preventive maintenance that clinicians can offer study participants who use tobacco. There is lack of preparedness among primary care physicians in delivering cessation interventions. There are also limited studies which record the effectiveness of cessation interventions in the Indian context. This study is designed to evaluate the effectiveness of brief and intensive tobacco cessation interventions delivered by trained primary care providers in two states of India. Methods and Analysis: A quasi-experimental study design has been adopted for the study with around 20 primary care practices, selected from four districts of two states in India (Odisha and Rajasthan). Brief (3A) and Intensive tobacco (5A) cessation intervention services will be provided to two groups of tobacco users, respectively. Both groups will be followed up for 6 months to determine the effectiveness of the cessation interventions. The cost-effectiveness of the services will also be documented at the end of the study. The entire study will be completed in 24 months, of which the final 6 months will be reserved for study participant follow-up and quit rate evaluation. When comparing the two groups, differences between proportions will be assessed by chi-square test and differences between means with t -test. The conventional significance level of 0.05 will be used in all analyses in order to reject the null hypothesis of no difference between groups. We will use difference-in-differences methods to assess the impact of the interventions on physicians’ behavior to deliver tobacco cessation in their clinical practice. Conclusion: The study is in participant recruitment phase.https://doi.org/10.1177/2050312117697173
collection DOAJ
language English
format Article
sources DOAJ
author Rajmohan Panda
Sandeep Mahapatra
Kumar Gaurav
Sanghamitra Pati
Manu Raj Mathur
spellingShingle Rajmohan Panda
Sandeep Mahapatra
Kumar Gaurav
Sanghamitra Pati
Manu Raj Mathur
A quasi-experimental intervention to assess the effectiveness of a physician-delivered tobacco cessation intervention in India: A detailed study protocol
SAGE Open Medicine
author_facet Rajmohan Panda
Sandeep Mahapatra
Kumar Gaurav
Sanghamitra Pati
Manu Raj Mathur
author_sort Rajmohan Panda
title A quasi-experimental intervention to assess the effectiveness of a physician-delivered tobacco cessation intervention in India: A detailed study protocol
title_short A quasi-experimental intervention to assess the effectiveness of a physician-delivered tobacco cessation intervention in India: A detailed study protocol
title_full A quasi-experimental intervention to assess the effectiveness of a physician-delivered tobacco cessation intervention in India: A detailed study protocol
title_fullStr A quasi-experimental intervention to assess the effectiveness of a physician-delivered tobacco cessation intervention in India: A detailed study protocol
title_full_unstemmed A quasi-experimental intervention to assess the effectiveness of a physician-delivered tobacco cessation intervention in India: A detailed study protocol
title_sort quasi-experimental intervention to assess the effectiveness of a physician-delivered tobacco cessation intervention in india: a detailed study protocol
publisher SAGE Publishing
series SAGE Open Medicine
issn 2050-3121
publishDate 2017-03-01
description Introduction: Tobacco cessation is the most important, cost-effective preventive maintenance that clinicians can offer study participants who use tobacco. There is lack of preparedness among primary care physicians in delivering cessation interventions. There are also limited studies which record the effectiveness of cessation interventions in the Indian context. This study is designed to evaluate the effectiveness of brief and intensive tobacco cessation interventions delivered by trained primary care providers in two states of India. Methods and Analysis: A quasi-experimental study design has been adopted for the study with around 20 primary care practices, selected from four districts of two states in India (Odisha and Rajasthan). Brief (3A) and Intensive tobacco (5A) cessation intervention services will be provided to two groups of tobacco users, respectively. Both groups will be followed up for 6 months to determine the effectiveness of the cessation interventions. The cost-effectiveness of the services will also be documented at the end of the study. The entire study will be completed in 24 months, of which the final 6 months will be reserved for study participant follow-up and quit rate evaluation. When comparing the two groups, differences between proportions will be assessed by chi-square test and differences between means with t -test. The conventional significance level of 0.05 will be used in all analyses in order to reject the null hypothesis of no difference between groups. We will use difference-in-differences methods to assess the impact of the interventions on physicians’ behavior to deliver tobacco cessation in their clinical practice. Conclusion: The study is in participant recruitment phase.
url https://doi.org/10.1177/2050312117697173
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