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Clinical Trials/NCT01935505
NCT01935505UnknownNot Applicable

Study on the Model of Smoking Cessation Intervention and Service Ability Improvement in General Hospital

Chinese PLA General Hospital0 sites2,000 target enrollmentStarted: October 2008Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
2,000
Primary Endpoint
quitting rate

Study Overview

Brief Summary

This is a observation non-randomized control trial, and a follow-up study on the smoking cessation.

Detailed Description

This is a observation non-randomized control trial, and a follow-up study on the smoking cessation.

To study the intervention methods of smoking cessation in a general hospital and to evaluate their effects. Four methods of specialist intervention of smoking cessation clinic, short-time intervention in out patients, free medical intervention and group intervention were adopted for different smokers, with health counseling, psychological intervention and drug treatment. The intervention effect was evaluated by standard methods.

The whole project will last for 10 years in total, from Oct.2008 to Dec.2018. During the running, each quitter received follow-up at 1 week, 1, 3, 6 months and 1, 2 years using a detailed questionnaire by telephone interview, an expected average of 2 years.

Study Design

Study Type
Observational
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • current smoker aged 18 years or above, Chinese,
  • agreed to participate in the follow-up and signed an informed consent form.

Exclusion Criteria

  • cognitively impaired and with severe diseases,
  • occasional or daily smoker,
  • Disagree and non-signed an informed consent form.

Arms & Interventions

Consulting group

The physicians adopted a non-directive approach, included the five 'A' (ask, advice, assess, assist and arrange), assessing the stage of readiness in quitting smoking, strengthening clients' motivation to quit smoking using the five 'R' (relevance, risks, rewards, roadblocks and repetition) approach, and providing advice to overcome psychological craving, psychological dependence and social-cultural factors associated with tobacco dependency. Each smoker takes more than 30 min to complete the intervention.

Intervention: Consulting (Behavioral)

Drug intervention group

According to the smokers' level of nicotine dependency, disease history, cigarette consumption, prescription of drugs were provided, Nicotine Replacement Therapy, bupropion and varenicline.

Intervention: Consulting (Behavioral)

Drug intervention group

According to the smokers' level of nicotine dependency, disease history, cigarette consumption, prescription of drugs were provided, Nicotine Replacement Therapy, bupropion and varenicline.

Intervention: Nicotine patch (Drug)

Drug intervention group

According to the smokers' level of nicotine dependency, disease history, cigarette consumption, prescription of drugs were provided, Nicotine Replacement Therapy, bupropion and varenicline.

Intervention: Telephone intervention (Behavioral)

Telephone intervention group

Smokers received follow-up by a counselor at 1 week, 1, 3, 6 months and 1, 2 years using a detailed questionnaire by telephone interview. At each follow-up, we collected data, asked whether the smokers have any problem with drug use or other problems, provided problem-oriented suggestions or advice as appropriate, encouraged them to insist.

Intervention: Consulting (Behavioral)

Telephone intervention group

Smokers received follow-up by a counselor at 1 week, 1, 3, 6 months and 1, 2 years using a detailed questionnaire by telephone interview. At each follow-up, we collected data, asked whether the smokers have any problem with drug use or other problems, provided problem-oriented suggestions or advice as appropriate, encouraged them to insist.

Intervention: Telephone intervention (Behavioral)

Consulting+Telephone+Drug intervention

All the interventions above are include in this group

Intervention: Consulting+Telephone+Drug intervention (Behavioral)

Outcomes

Primary Outcomes

quitting rate

Time Frame: up to 10 years

The whole project will last for 10 years in total, from Oct.2008 to Dec.2018. During the running, each participant will be followed by telephone tracking, an expected average of 2 years.

Secondary Outcomes

  • decrease of tobacco consumption(up to 10 years)

Investigators

Sponsor
Chinese PLA General Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Yao He

Institute of Geriatrics

Chinese PLA General Hospital

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