Smoking Reduction Intervention for Smokers Not Willing to Quit Smoking: a Randomised Control Trial

NCT ID: NCT00563329

Last Updated: 2013-10-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

3826 participants

Study Classification

INTERVENTIONAL

Study Start Date

2004-10-31

Study Completion Date

2006-07-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The aims of this study are (1) to examine the effect of smoking reduction intervention (reduction counseling and nicotine replacement therapy, NRT) (a) on smoking cessation and (b) on reducing daily cigarette consumption among smokers not willing to quit smoking but want to reduce smoking, and (2) to examine the effect of adherence intervention in producing a higher (a) adherence rate, (b) reduction rate, and (c) quit rate.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Smoking Cessation

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Smokers who are not willing to quit in the near future but intend to reduce smoking

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Blinding Strategy

SINGLE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Reduction Intervention + Adherence Intervention

Intervention Type PROCEDURE

Reduction Intervention

Intervention Type BEHAVIORAL

control

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Age 18 or above
* Ethnic Chinese male or female
* Smokes at least 2 cigarettes per day
* Have no intention to quit in the near future
* Intends to reduce smoking in the next 7 days
* Has no contraindication to NRT

Exclusion Criteria

* Subjects who are psychologically or physically unable to communicate
* Children and teenagers (age below 18)
* Pregnant or intention to become pregnant within the next 6 months
* Those on regular psychotropic medications and in the presence of any serious health problems that may make them unsuitable for using NRT, such as recent stroke, palpitation, or other life threatening conditions
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

The University of Hong Kong

OTHER

Sponsor Role collaborator

Hospital Authority, Hong Kong

OTHER_GOV

Sponsor Role lead

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

TH Lam, Prof

Role: PRINCIPAL_INVESTIGATOR

Department of Community Medicine, Faculty of Medicine, The University of Hong Kong

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

HAHO

Hong Kong, , China

Site Status

Hong Kong Council on Smoking and Health

Hong Kong, , China

Site Status

The University of Hong Kong

Hong Kong, , China

Site Status

Countries

Review the countries where the study has at least one active or historical site.

China

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

HARECCTR0500051

Identifier Type: -

Identifier Source: secondary_id

UW 03-103 T/103

Identifier Type: -

Identifier Source: org_study_id