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Not yet recruiting NCT06663475

A TTM-based Smoking Cessation Intervention in Helping Expectant Fathers to Quit Smoking and Maintain Abstinence

No phase Interventional Smoking Cessation Behavioral Intervention

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: TTM-based health education videos about smoking cessation for expectant fathers, usual care treatment.
Who it may be relevant to
Registry conditions: Smoking Cessation, Behavioral Intervention. Basic parameters: from 18 years · Male.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

The Effectiveness of a Transtheoretical Model Based Health Education Intervention in Smoking Cessation Among Expectant Fathers: a Randomized Control Trial

Overview

This study aims to evaluate the effectiveness of the video-based health education in smoking cessation among expectant fathers by using two-arm randomized clinical trial to motivate this subgroup attempt to quit, quit smoking and maintain abstinence in the long term.

Interventions

  • Behavioral TTM-based health education videos about smoking cessation for expectant fathers
    Tailored for expectant fathers, this smoking cessation health education information will be developed based on transtheoretical model to motivate a quit attempt and maintain abstinence by using videos.
  • Behavioral usual care treatment
    general health education videos about hazards of smoking for expectant fathers in obstetric clinic

Primary outcome measures

  • Biochemically validated smoking abstinence [Time frame: 12 month follow-up after randomization]
Secondary outcome measures (7)
  • Self-reported 7-day point prevalence quit rate [Time frame: 6, 12-month follow-up]
  • Smoking Reduction [Time frame: end of intervention; 3,6,12 month after randomization]
  • Quit Attempt [Time frame: end of intervention; 3,6,12 month after randomization]
  • The change in transtheoretical model stages [Time frame: end of intervention; 3,6,12 month after randomization]
  • the Fagerstrom tolerance questionnaire [Time frame: end of intervention; 3,6,12 month after randomization]
  • Use of smoking cessation services [Time frame: end of intervention; 3,6,12 month after randomization]
  • Biochemically validated smoking abstinence [Time frame: 6 month follow-up]

Eligibility criteria

Inclusion criteria

  • male adult
  • has a pregnant partner
  • at least smoke 1 cigarette per day on average in the last month
  • be able to read or communicate in Chinese

Exclusion criteria

  • be or was participated in other smoking cessation program in the past year
  • mentally or physically unable to communicate with
  • can't play videos by electronic devices
  • the pregnant partner is a smoker

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Supportive care

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06663475 · L2023SYSU-HL-027 · 72104259

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗