BMC Public Health

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Open Access Study protocol

Efficacy of smoking prevention program 'Smoke-free Kids': study protocol of a randomized controlled trial

Marieke Hiemstra1*, Linda Ringlever1, Roy Otten1, Christine Jackson2, Onno CP van Schayck3 and Rutger CME Engels1

Author Affiliations

1 Behavioural Science Institute, Radboud University Nijmegen, Nijmegen, P.O. Box 9104, 6500 HE Nijmegen, The Netherlands

2 Community Health Promotion Research, RTI International, P.O. Box 12194, Research Triangle Park, NC 27709-2194, USA

3 Department of General Practice, Maastricht University, P.O. Box 616, 6200 MD Maastricht, The Netherlands

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BMC Public Health 2009, 9:477 doi:10.1186/1471-2458-9-477

Published: 21 December 2009

Abstract

Background

A strong increase in smoking is noted especially among adolescents. In the Netherlands, about 5% of all 10-year olds, 25% of all 13-year olds and 62% of all 17-year olds report ever smoking. In the U.S., an intervention program called 'Smoke-free Kids' was developed to prevent children from smoking. The present study aims to assess the effects of this home-based smoking prevention program in the Netherlands.

Methods/Design

A randomized controlled trial is conducted among 9 to 11-year old children of primary schools. Participants are randomly assigned to the intervention and control conditions. The intervention program consists of five printed activity modules designed to improve parenting skills specific to smoking prevention and parent-child communication regarding smoking. These modules will include additional sheets with communication tips. The modules for the control condition will include solely information on smoking and tobacco use.

Initiation of cigarette smoking (first instance of puffing on a lighted cigarette), susceptibility to cigarette smoking, smoking-related cognitions, and anti-smoking socialization will be the outcome measures. To collect the data, telephone interviews with mothers as well as with their child will be conducted at baseline. Only the children will be examined at post-intervention follow-ups (6, 12, 24, and 36 months after the baseline).

Discussion

This study protocol describes the design of a randomized controlled trial that will evaluate the effectiveness of a home-based smoking prevention program. We expect that a significantly lower number of children will start smoking in the intervention condition compared to control condition as a direct result of this intervention. If the program is effective, it is applicable in daily live, which will facilitate implementation of the prevention protocol.

Trial registration

Netherlands Trial Register NTR1465