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Mobile Motivational Messages for Change (3M4Chan) Intervention in TMU

T

Taipei Medical University

Status

Completed

Conditions

Explore Successful Method to Quit Smoking

Treatments

Other: Case

Study type

Interventional

Funder types

Other

Identifiers

NCT03108651
N201702069

Details and patient eligibility

About

About 100 (50 from TMU Hospital and 50 from Wellcome Clinic) current smokers will be recruited who contact smoke cession clinics in teaching hospitals of Taipei Medical University (TMU) and Wellcome Clinic. They will be randomly assigned either to Usual Care (UC) or Usual Care plus 3M4Chan Intervention group (IG). A randomized comparative effectiveness trial will be conducted. Patient will enroll from September 2017 to May 2018. In UC group, the physician provides a brief advice to quit during first consultation, a quit plan template, and medication prescription (Varenicline, Bupropion, Champix, Nicotinell TTS20) as decided by the physician. IG group includes UC plus a mobile App that is programmed to push tailored messages for health concern and readiness to quit, tips for sustaining abstinence, use of interactive self-assessments, helpful cessation information. This group of smokers will benefit from tailored cessation interventions with integrated body weight management elements that take into consideration the prevailing local and cultural influences on diet and levels of physical activity. IG will be continued even after stopping of the UC.

Enrollment

92 patients

Sex

All

Ages

20+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age 20 years or older and approach smoke cessation clinic at TMU hospital
  • Have an Android mobile phone
  • Able to read Traditional Chinese
  • Willing to participate in all study components
  • Willing to be followed-up for 6 months
  • Smoked at least once every month in the last two years
  • Current smoker

Exclusion criteria

  • • Below 20 years on the day of enrolment

    • Not willing to participate in the study
    • Those who do not have Android mobile phone or unable to read Mandarin
    • Not willing to share medical information from EHR
    • Subjects who develop adverse effects related to the pharmacological treatment included in the study

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

92 participants in 2 patient groups

Case
Active Comparator group
Description:
Motivational message will be administrated.
Treatment:
Other: Case
Control
No Intervention group
Description:
Motivational message will not be administrated.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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