Helping Youth Smokers Stop Smoking Through the Youth Quitline Programme
1 other identifier
interventional
300
1 country
1
Brief Summary
The aims of the present study are:
- 1.To raise the awareness of smoking cessation service among youth smokers in Hong Kong;
- 2.To provide smoking cessation quitline service to youth smokers; and
- 3.To provide training to teenagers as peer smoking cessation counsellors.
- 4.To examine the effectiveness of adventure-based training and WhatsApp messages in helping youth smokers to quit
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Aug 2005
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 1, 2005
CompletedFirst Submitted
Initial submission to the registry
April 28, 2016
CompletedFirst Posted
Study publicly available on registry
May 2, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2021
CompletedDecember 14, 2020
April 1, 2020
16.3 years
April 28, 2016
December 11, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
7-days point prevalence smoking abstinence at 6-month
7-days point prevalence smoking abstinence is measured at 6-month. A questionnaire asking smoking status, quitting experience and difficulty in quitting was designed to assess the self-reported smoking abstinence at 6-month.
6-month follow-up
Secondary Outcomes (1)
Bio-chemical validated smoking abstinence at 6-month
6-month follow-up
Study Arms (1)
Brief counseling
OTHERPeer counselling is delivered based on the queries and the needs of individual clients, according to the smoking status, dependency level and the perceived barriers of each individual with the use of motivational intervention approach. Counsellors will emphasizes the identification, use, and modification of personally relevant coping strategies. Advice will be provided on overcoming expected difficulty, withdrawal symptoms and relapse prevention during quitting. The subjects will be followed up at 1-week, 1-, 3-, 6-, 9-, 12- and 24-month via telephone assessing their smoking status and reinforce intervention.
Interventions
Peer counselling is delivered based on the queries and the needs of individual clients, according to the smoking status, dependency level and the perceived barriers of each individual with the use of motivational intervention approach. The subjects will be followed up at 1-week, 1-, 3-, 6-, 9-, 12- and 24-month via telephone assessing their smoking status and reinforce intervention.
Eligibility Criteria
You may qualify if:
- Hong Kong resident aged 25 or below
- Able to communicate in Chinese (Cantonese)
- Smoked in the past 30 days
You may not qualify if:
- Have difficulty to communicate via telephone
- Having queries irrelevant to tobacco control
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The University of Hong Kong
Hong Kong, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ho-Cheung Li, PhD
The University of Hong Kong
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
April 28, 2016
First Posted
May 2, 2016
Study Start
August 1, 2005
Primary Completion
November 1, 2021
Study Completion
November 1, 2021
Last Updated
December 14, 2020
Record last verified: 2020-04
Data Sharing
- IPD Sharing
- Will share
- Time Frame
- After the project is completed and the results of the project has been published.
- Access Criteria
- Request could be sent to Principal Investigator (william3@hku.hk)
The relevant anonymized patient level data, full dataset, technical appendix, and statistical code are available on reasonable request. The approval from the Principal Investigator for the purpose of data use is required.