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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00563199
Other study ID # NTWC/CREC/325/04
Secondary ID HARECCTR0500022H
Status Completed
Phase N/A
First received November 21, 2007
Last updated June 14, 2011
Start date March 2002
Est. completion date December 2005

Study information

Verified date June 2011
Source Hospital Authority, Hong Kong
Contact n/a
Is FDA regulated No
Health authority Hong Kong: Ethics Committee
Study type Interventional

Clinical Trial Summary

This study is a randomized controlled trial designed to evaluate the effectiveness of a nurse delivered stage-matched intervention to cardiac patients for cessation of tobacco use. Review of literature shows that there is a clear lack of empirical evidence on (1) using nurses to deliver stage-matched smoking cessation interventions, and (2) the effectiveness of such intervention for cardiac patients in Chinese populations. The ultimate goal of the intervention achieve a higher quit rate in the intervention group than in the controls. In addition, the change in the patient's smoking behaviour such as reduction of the number of cigarettes smoked, and progression to a higher stage of readiness to quit, will also be measured. This study is the first step to address the urgently needed data for (1) promoting the delivery of nurse-run stage-matched smoking cessation interventions to help patients stop smoking, (2) developing smoking cessation policy and programmes in the hospitals and for the health care system, and (3) contributing an evidence-based approach to orientate clinical services towards prevention, so as to reduce premature deaths and the enormous disease burden of our society.


Recruitment information / eligibility

Status Completed
Enrollment 1824
Est. completion date December 2005
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Patient who is admitted to the participating centres and is a current smoker who has smoked daily in the past 7 days prior to hospitalization.

- Patient speaks and reads Cantonese/Chinese

Exclusion Criteria:

- Patient who is clinically too ill and not suitable to complete questionnaire and/or receive intervention.

- Patient who does not speak or read Chinese

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind


Related Conditions & MeSH terms


Intervention

Behavioral:
nurse-delivered stage-matched smoking cessation counseling


Locations

Country Name City State
China Caritas Medical Centre Hong Kong
China Pamela Youde Nethersole Eastern Hospital Hong Kong
China Princess Margaret Hospital Hong Kong
China Queen Elizabeth Hospital Hong Kong
China Queen Mary Hospital Hong Kong
China Ruttonjee Hospital / Tang Shiu Kin Hospital Hong Kong
China Tseung Kwan O Hospital Hong Kong
China Tuen Mun Hospital Hong Kong
China Tung Wah Hospital Hong Kong
China United Christian Hospital Hong Kong

Sponsors (2)

Lead Sponsor Collaborator
Hospital Authority, Hong Kong The Hong Kong Research Grants Council (RGC)

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quitting--to achieve higher quit rate in the cardiac patients (coronary artery disease) who are smokers continuous abstinence for one month at the time of 3, 6 and 12 month follow up
Secondary Reduction of the number of cigarettes smoked at the time of 3, 6 and 12 month follow up
Secondary Progression to a higher stage of readiness to quit at the time of 3, 6 and 12 month follow up
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