跳至主要内容
临床试验/NCT03879889
NCT03879889已完成4 期

Smoking Reduction Intervention for Smoking Parents of Paediatric Patients in Hong Kong: a Randomised Controlled Trial

Chinese University of Hong Kong1 个研究点 分布在 1 个国家目标入组 210 人开始时间: 2017年2月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
210
试验地点
1
主要终点
Validated successful smoking reduction rate

研究概览

简要总结

A randomized controlled trial to evaluate the effectiveness of smoking reduction interventions for smoking parents in paediatric hospital setting in Hong Kong.

详细描述

This is a single blinded randomized controlled trial aiming to evaluate the effectiveness of smoking reduction interventions for smoking parents in paediatric hospital setting in Hong Kong. This trial consists of a 24-week intervention period. Eligible families will be randomly assigned to either intervention group or control group. Smoking parent(s) in intervention group will be given face-to-face counselling on smoking reduction and adherence to nicotine replacement therapy (NRT) with motivational interviews, provision of NRT and monthly phone follow-up for counselling and support. Smoking parent(s) in control group will be given standard advice and information on smoking cessation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Investigator, Outcomes Assessor)

盲法说明

Research study personnel who will conduct the data collection on outcome measures will be blinded to the group assignment. The researchers who will conduct the data analysis will also be blinded the group assignment.

入排标准

性别
All
接受健康志愿者

入选标准

  • Ethnic Chinese family with children aged younger than 18 years of age.
  • Children who are admitted to the paediatric inpatient units or attend the paediatric specialist clinic at the Prince of Wales Hospital.
  • Children with at least one custodial smoking parent who is living with them.
  • Written informed consent obtained from parents.

排除标准

  • Families not residing in Hong Kong.
  • Children in foster care.
  • Children with unclear custody.
  • Smoking paediatric patients.
  • Presence of smoking household members apart from the parents.
  • Smoking parent who is contraindicated to use nicotine replacement therapy.

研究组 & 干预措施

Intervention

Experimental

Intervention arm will include face-to-face counseling on smoking reduction and adherence to nicotine replacement therapy (NRT) with motivational interviews, provision of free NRT, referral to quit smoking hotline, monthly phone follow-up and two follow-up visits.

干预措施: Nicotine patch (Drug)

结局指标

主要结局

Validated successful smoking reduction rate

时间窗: Week-24

Urinary cotinine validated parental successful smoking reduction rate at week-24

Self-reported parental successful smoking reduction rate at week-24

时间窗: Week-24

Self-reported reduction of daily cigarette consumption by 50% or more compared with baseline

次要结局

  • Urinary cotinine validated parental smoking cessation rate at week-24(Week-24)
  • Change in children's urinary cotinine level from baseline to week-24(Week-24)
  • Parental self-reported smoking reduction rate of cigarette consumption(Week-24)
  • Parental self-reported smoking cessation rate of cigarette consumption(Week-24)

研究者

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

Kate Ching Ching Chan

Clinical Professional Consultant

Chinese University of Hong Kong

研究点 (1)

Loading locations...

相似试验

Smoking Reduction Intervention for Smoking Parents... | 临床试验