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临床试验/NCT06399588
NCT06399588尚未招募不适用

Intervention for Adolescent Tobacco Initiation Prevention (IATIP) to Promote Health and Well-being: A Protocol for a Pilot Feasibility Cluster Randomised Controlled Trial in Dhaka, Bangladesh

University College, London1 个研究点 分布在 1 个国家目标入组 1,280 人开始时间: 2024年5月2日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
1,280
试验地点
1
主要终点
Feasibility of the intervention: fidelity of delivery

研究概览

简要总结

This school-based cluster randomized controlled trial aims to assess the feasibility of implementing the Adolescent Tobacco Initiation Prevention (IATIP) and evaluate the potential efficacy of IATIP in preventing tobacco initiation and promoting the health and well-being of school adolescents in Dhaka, Bangladesh. The intervention consists of three 40-minute sessions, delivered over three successive days, including knowledge and skill-based lectures, interactive activities, and materials targeting tobacco prevention and health promotion.

详细描述

Background and Aims: Adolescent tobacco use is a significant public health challenge, particularly in low- and middle-income countries like Bangladesh. An Intervention for Adolescent Tobacco Initiation Prevention (IATIP) has been developed to address this issue. This study aims to assess the feasibility of implementing the IATIP and evaluate its potential efficacy in preventing tobacco initiation and promoting health and well-being.

Design: Pilot feasibility school-based cluster randomized controlled trial.

Setting: Secondary schools in Dhaka city, Bangladesh.

Participants: Adolescents in school years 8 and 9 attending participating schools in Dhaka (K = 8 clusters; N~1280 participants).

Intervention: The intervention consists of three 40-minute sessions, delivered over three successive days, including knowledge and skill-based lectures, interactive activities, and materials targeting tobacco prevention and health promotion. This intervention was developed based on evidence gathered from a quantitative survey, qualitative focus groups, and a systematic review.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

年龄范围
11 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Bangladeshi school adolescent
  • Students at one of the participating schools
  • Students of Years 8 and 9

排除标准

  • Students of physical and mental impairment
  • don't understand and read the 'Bangla' language
  • don't have parental consent

结局指标

主要结局

Feasibility of the intervention: fidelity of delivery

时间窗: Immediately after the completion of the intervention delivery, an average of 30 days.

The fidelity of intervention delivery will be assessed using a pre-defined index, consisting of 21 content items. A 3-point Likert (0 = not implemented, 1 = partially implemented and 2 = fully implemented) will be used to assess the fidelity index. A higher score indicates a more fidelity of intervention delivery.

Feasibility of the intervention: attrition rate

时间窗: Through study completion, an average of 2 months.

The dropout rate will be monitored as a measure of attrition, specifically, calculating the percentage of recruited participants who do not complete the follow-up assessment.

Feasibility of the intervention: recruitment rate

时间窗: Before starting the intervention, an average of 10 days.

The percentage of eligible participants who agree to take part in the study will be calculated to evaluate recruitment rate.

Feasibility of the intervention: acceptability

时间窗: Immediately after the completion of the intervention delivery, an average of 30 days.

To evaluate the acceptability of the intervention, participants' perceptions of the intervention's relevance, and appropriateness will be explored. Participants will be asked a 5-point Likert scale question: "To what extent do you feel the study sessions met your expectations?", with response options ranging from 1 (not at all) to 5 (completely). They will also be asked, "To what extent do you think the components were relevant to preventing tobacco initiation and promoting health and well-being?" and "To what extent do you think the images and videos presented in the sessions were appropriate and relevant to the contents?" with the same measures. The clarity and comprehensibility of the intervention materials, such as handbooks and presentations, will be rated on a 5-point Likert scale from 1 (not at all) to 5 (extremely). A higher score indicates a more acceptable intervention.

次要结局

  • Change in the intention to initiate tobacco use(Up to 5 weeks)
  • Evaluate the promotion of overall mental well-being(Up to 5 weeks)
  • Change in stress score(Up to 5 weeks)
  • Skill development: Refusal skill(Up to 5 weeks)
  • Skill development: Problem solving(Up to 5 weeks)
  • Change in self-rated physical health score(Up to 5 weeks)
  • Change in anxiety score(Up to 5 weeks)
  • Change in knowledge(Up to 5 weeks)
  • Skill development: Assertiveness(Up to 5 weeks)
  • Change in depression score(Up to 5 weeks)
  • Change in attitudes(Up to 5 weeks)
  • Change in beliefs(Up to 5 weeks)
  • Skill development: Decision-making(Up to 5 weeks)
  • Skill development: Self-esteem(Up to 5 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sahadat Hossain

Principal Investigator

University College, London

研究点 (1)

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