A Randomized Controlled Trial on Smoking Cessation and Adherence Intervention on Patients With Erectile Dysfunction

NCT ID: NCT00563511

Last Updated: 2011-06-16

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

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

1210 participants

Study Classification

INTERVENTIONAL

Study Start Date

2004-01-31

Study Completion Date

2006-08-31

Brief Summary

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The purpose of this proposed RCT is to test (a) the effectiveness of smoking cessation intervention (counseling and NRT) among patients with ED; and (b) the effectiveness of adherence intervention (ADIN) to increase adherence to NRT use in order to increase quit rate.

Detailed Description

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Conditions

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Smoking Cessation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Blinding Strategy

SINGLE

Interventions

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adherence intervention

Intervention Type PROCEDURE

intervention without adherence advice

Intervention Type PROCEDURE

control

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Male ethnic Chinese aged 18 or above
* Smokes at least 1 cigarette per day
* Is not following other forms of smoking cessation interventions
* Intends to quit smoking within the next 7 days of the first contact and would use NRT
* Free from illness that contraindicate to the use of NRT
* Has signed an informed consent form, or has given verbal consent (for those contacted by telephone)

Exclusion Criteria

* Patients who are psychologically or physically unable to communicate
* Children and teenagers (aged below 18)
* 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

MALE

Accepts Healthy Volunteers

No

Sponsors

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The University of Hong Kong

OTHER

Sponsor Role collaborator

Hospital Authority, Hong Kong

OTHER_GOV

Sponsor Role lead

Principal Investigators

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TH Lam, Prof

Role: PRINCIPAL_INVESTIGATOR

Department of Community Medicine, The University of Hong Kong

Locations

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HKFPA

Hong Kong, , China

Site Status

Kwong Wah Hospital

Hong Kong, , China

Site Status

The University of Hong Kong

Hong Kong, , China

Site Status

WHO

Hong Kong, , China

Site Status

Countries

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China

Other Identifiers

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HARECCTR0500052

Identifier Type: -

Identifier Source: secondary_id

HKU7428/03M

Identifier Type: -

Identifier Source: secondary_id

EC1966-02

Identifier Type: -

Identifier Source: org_study_id

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