ClinicalTrials.gg
Not yet recruitingNCT07758998Updated Aug 11, 2026

The Effect of Motivational Interviewing on Smoking Behavior Among Nursing Students

An interventional study of Transtheoretical Model-Based Motivational Interviewing in Tobacco Use and Smoking Cessation, sponsored by Meral Feratoğlu Research. Not yet recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-11.

Sponsored by Meral Feratoğlu Research · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
87
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

Smoking is one of the leading preventable public health problems worldwide, particularly among young adults who are at increased risk of nicotine dependence. Nursing students represent an important target population because, as future health professionals, they are expected to play a significant role in tobacco control and smoking cessation counseling. The Transtheoretical Model (TTM) is one of the most widely used theoretical frameworks for promoting health behavior change. The aim of this study will be to determine the effect of Transtheoretical Model-based motivational interviewing on changing smoking behavior among nursing students.

This study will be planned as a single-group, quasi-experimental pretest-posttest intervention. Nursing students who smoke cigarettes and voluntarily agree to participate will be included in the study. At baseline, participants will complete a Demographic Information Form, the Fagerström Test for Nicotine Dependence, the Stages of Change questionnaire, the Self-Efficacy/Temptation Scale, the Processes of Change Scale, and the Decisional Balance Scale.

Participants will receive Transtheoretical Model-based educational sessions and motivational interviewing interventions focusing on the health effects of smoking, reasons for smoking, the benefits of smoking cessation, identification of social support resources, relapse prevention strategies, and successful smoking cessation experiences. The Stages of Change questionnaire will be administered before each motivational interviewing session, and all outcome measures will be reassessed during follow-up evaluations. The study is expected to provide evidence regarding the effectiveness of Transtheoretical Model-based motivational interviewing in reducing smoking behavior, decreasing nicotine dependence, promoting progression through the stages of change, improving self-efficacy, enhancing the use of behavioral change processes, and supporting smoking cessation among nursing students.

02

Conditions studied

  • Tobacco Use
  • Smoking Cessation

Keywords

  • motivational interviewing
  • Transtheoretical Model
  • Nursing Students
  • Smoking Cessation
  • Tobacco Use
  • Smoking Behavior
03

In context

Tobacco Use

420 studies on the registry are indexed under Tobacco Use; 82 are open to participants now.

This study's planned enrollment of 87 is below the median of 124 across 351 interventional studies indexed under Tobacco Use.

Browse Tobacco Use studies →

Lead sponsor

This is the only study on the registry with Meral Feratoğlu Research as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Nursing students currently enrolled in the study setting.
  • Aged 18 years or older.
  • Current cigarette smokers.
  • No self-reported health condition that would prevent participation in the intervention.
  • Willing and able to provide and participate in the study.

Exclusion criteria

Exclusion Criteria:

  • Inability to complete all planned stages of the study.
  • Withdrawal of consent or voluntary discontinuation from the study at any time.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
87 participants (estimated)

Study arms

  • Experimental
    Motivational Interviewing

    Participants will receive a Transtheoretical Model-based motivational interviewing intervention designed to promote smoking behavior change and smoking cessation. The intervention will consist of structured face-to-face motivational interviewing sessions delivered in groups, supported by educational content on the health effects of smoking, benefits of smoking cessation, behavior change strategies, social support, relapse prevention, and self-efficacy enhancement. Outcomes will be evaluated using validated questionnaires administered at baseline and follow-up assessments.

    Behavioral: Transtheoretical Model-Based Motivational Interviewing

Interventions

  • BehavioralTranstheoretical Model-Based Motivational Interviewing

    Participants will receive a Transtheoretical Model-based motivational interviewing intervention to promote smoking behavior change and smoking cessation. Face-to-face motivational interviewing sessions will be conducted by a researcher trained in motivational interviewing. According to the intervention protocol, participants may receive between two and six sessions depending on their readiness to change, individual needs, and continued participation throughout the study. The intervention will include counseling and education on smoking-related health risks, smoking cessation, motivation enhancement, self-efficacy, behavior change strategies, social support, and relapse prevention. Participants' stage of change will be assessed before each session, and the intervention will be tailored accordingly. Outcomes will be evaluated using validated instruments measuring smoking behavior, nicotine dependence, stages of change, self-efficacy, and behavior change processes.

06

What researchers measure

Primary outcomes

  1. Change in Smoking Behavior

    The primary outcome is the change in smoking behavior following the Transtheoretical Model-based motivational interviewing intervention. Smoking behavior will be evaluated by the average number of cigarettes smoked per day and smoking cessation status.

    Time frame: Baseline, Mid-intervention Assessment (1 month), Post-intervention Assessment (2 months)

Secondary outcomes

  1. Change in Nicotine Dependence

    Nicotine dependence will be assessed using the Fagerström Test for Nicotine Dependence (FTND). The total score ranges from 0 to 10, with higher scores indicating a higher level of nicotine dependence.

    Time frame: Baseline, Mid-intervention Assessment (1 month later), Post-intervention Assessment (2 months later)

  2. Change in Processes of Change

    Behavioral change processes will be assessed using the Processes of Change Scale. The total score ranges from 22 to 110, with higher scores indicating greater use of behavioral change processes related to smoking cessation.

    Time frame: Baseline, Mid-intervention Assessment( 1 month later), Post-intervention Assessment (2 months later)

  3. Change in Self-Efficacy/Temptation for Smoking Cessation

    Self-efficacy related to smoking cessation will be assessed using the Self-Efficacy/Temptation Scale. The scale consists of 8 items rated on a 5-point Likert scale, with a total score ranging from 8 to 40. Higher scores indicate greater self-efficacy and greater confidence in the ability to refrain from smoking in situations that may trigger the urge to smoke.

    Time frame: Baseline, Mid-intervention Assessment (1 month later), Post-intervention Assessment (2 months later)

  4. Change in Decisional Balance

    Decisional balance related to smoking cessation will be assessed using the Decisional Balance Scale. The scale consists of 12 items rated on a 5-point Likert scale, with a total score ranging from 12 to 60. Higher scores indicate greater perceived importance of the benefits and barriers of change and greater engagement in the decision-making process related to smoking cessation.

    Time frame: Baseline, Mid-intervention Assessment (1 month later), Post-intervention Assessment (2 months later)

07

Study locations

1 site
  • Kırklareli University Faculty of Health Sciences
    Kırklareli, Kırklareli 39100, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Aug 2026; primary completion for Sep 2026, 1 month later.

Of 167 non-industry interventional studies with no phase under Tobacco Use, half reached primary completion within 24 months of starting (the median), counting those still running; a quarter within 12 and three quarters within 41. This study's planned 1 month is below that.

Counting every sponsor, half of 223 studies reached it within 16 months; a quarter within 5 and three quarters within 33.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 5, 2026
First posted
Aug 11, 2026
StartEst.
Aug 2026
Primary completionEst.
Sep 2026
CompletionEst.
Dec 2026
Last update
Aug 11, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07758998
Lead sponsor
Meral Feratoğlu Research
Responsible party
Sponsor
First posted
Aug 11, 2026
Start date
Aug 2026 (estimated)
Primary completion
Sep 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Aug 11, 2026

Study contacts

Sevim Meral Feratoğlu, MSc
Contact
sevimmeralf@outlook.com
+905346674614

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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