NCT03556774

Brief Summary

In this single-blind, randomized trial, undertaken in China with 8-week interventions and follow-up to 52 weeks, about 2,200 providers will be randomly allocated to the intervention or control group.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
2,200

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Apr 2019

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 29, 2018

Completed
2 months until next milestone

First Posted

Study publicly available on registry

June 14, 2018

Completed
10 months until next milestone

Study Start

First participant enrolled

April 1, 2019

Completed
2.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 30, 2021

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 30, 2021

Completed
Last Updated

August 12, 2020

Status Verified

August 1, 2020

Enrollment Period

2.4 years

First QC Date

April 29, 2018

Last Update Submit

August 11, 2020

Conditions

Outcome Measures

Primary Outcomes (1)

  • The effectiveness of 'WeChat WeQuit' training program.

    The utilization rate (i.e. rate=smokers treated divided by smokers seen) of behavioral and pharmacotherapy interventions by HSP for smoking patients from 8 to 52-week.

    52 weeks

Secondary Outcomes (1)

  • Prevalence of smoking abstinence

    24 weeks

Study Arms (2)

With smoking cessation training

EXPERIMENTAL

Participants who allocate to the intervention group will receive regular smoking cessation training program messages by professional team. One to six messages will be sent per day for 8 weeks. Hand copy of behavioral and pharmacotherapy interventions manual will send to each HSP by mail after randomization. One to three messages will be sent per week until the end of the 1-year follow-up. They will also be encouraged to communicate the experience of using behavioral and pharmacotherapy interventions in their group.

Behavioral: 'WeChat WeQuit' smoking cessation training program

Without smoking cessation training

NO INTERVENTION

Control group participants will not receive any smoking cessation messages by professional team. They will receive messages of thanking them for being in the study and reminding them of the time until 52-week follow-up. One to six messages will be sent per week for 8 weeks. They will be encouraged to communicate the experience of helping patients quit smoking in their group.

Interventions

Providing 'WeChat WeQuit' smoking cessation training program for healthcare service providers (HSPs) and assessing their utilization of behavioral and pharmacotherapy interventions for cigarette smoking cessation.

With smoking cessation training

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Chinese-speaking healthcare service providers
  • Know how to use WeChat
  • Use WeChat on a daily basis
  • Willing to provide informed consent to participate in the study -

You may not qualify if:

  • Non-Chinese speakers
  • Not healthcare service providers
  • Do not use WeChat
  • Unwilling to participate in the study -

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Yanhui Liao

Hangzhou, Zhejiang, 310016, China

RECRUITING

Related Publications (1)

  • Wang Y, Peng P, Wu Z, Liu Y, Wang C, Tang J, Liao Y. Boosting Smoking Cessation Intervention Utilization in Chinese Health Care Providers: A Randomized Controlled Trial of the "WeChat WeQuit" Medical Education Program. Nicotine Tob Res. 2024 Dec 23;27(1):61-72. doi: 10.1093/ntr/ntae166.

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
INVESTIGATOR
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Attending Psychiatrist

Study Record Dates

First Submitted

April 29, 2018

First Posted

June 14, 2018

Study Start

April 1, 2019

Primary Completion

August 30, 2021

Study Completion

August 30, 2021

Last Updated

August 12, 2020

Record last verified: 2020-08

Locations