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CompletedNCT07577167Updated May 11, 2026

Examining a Smoking Cessation Program: The Impact of a Modified Motivational Interviewing Consultation Approach

An interventional study of Modified Motivational Interviewing in Smoking Cessation and Motivational Intervention, sponsored by Mohammed Al-Hammouri. Completed at 1 site in Jordan. Per ClinicalTrials.gov, last updated 2026-05-11.

Sponsored by Mohammed Al-Hammouri · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 11 months after the study started (first participant enrolled May 2025, registered Apr 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
200
Allocation
Randomized
Sex
All
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Study summary

The goal of this clinical trial is to learn if a Modified Motivational Interviewing (MMI) program can help university students quit smoking. The main questions it aims to answer are: Does the MMI program reduce physical nicotine dependence and increase motivation to quit smoking. Does the MMI program improve students' confidence and perceived importance regarding quitting smoking.

Researchers will compare a group receiving the MMI intervention to a control group (who receive no initial intervention) to see if the video-based program is an effective and cost-saving way to treat smoking behavior.

Participants will: Complete self-report surveys about their smoking habits and feelings toward quitting at the start of the study, after 8 weeks, and 3 months later.

Record two 15-minute videos per week for the first 2 weeks using a mobile phone or similar device. Record one 15-minute video per week for the next 2 weeks. Record one 15-minute video every 2 weeks for the final 4 weeks. Receive individualized feedback from researchers on the content of their videos to help guide their "change talk".Have the option to share their videos with other students in the program through a private, virtual online thread.

Read the detailed description

Study OverviewThe goal of this randomized controlled trial is to evaluate the effectiveness of a Modified Motivational Interviewing (MMI) intervention specifically designed for university students who smoke. While traditional Motivational Interviewing (MI) is effective, it often requires highly skilled practitioners and significant time, making it costly and difficult to implement widely in a campus setting. This study tests a simplified, cost-effective version of the approach that uses participant-recorded videos to facilitate "change talk".The Intervention (MMI)Participants assigned to the intervention group will participate in an 8-week program. They will use their own devices, such as cell phones, to record a series of 15-minute videos. These videos focus on four specific categories of change talk:Identifying the advantages of quitting smoking.Expressing optimism about their ability to change.Stating their intentions to change their behavior.Discussing the disadvantages of their current smoking status.Researchers provide individualized feedback on each video to ensure the content aligns with these categories before the participant moves on to the next recording. Participants also have the option to share their videos within a private, virtual thread to connect with others in the intervention group.Comparison and Data Collection The study compares the intervention group to a control group that receives no intervention during the active study period. Data is collected from both groups at three distinct time points: Baseline: Before the intervention begins. Post-Intervention: Immediately following the 8-week program. Follow-up: Three months after the program has ended to assess long-term behavior change. Objectives and Measurement The primary objective is to determine if there is a statistically significant difference between the two groups regarding several key smoking-related variables. The study will measure: Physical nicotine dependence using the Fagerstrom Test. Readiness and motivation to quit smoking. Reinforcing and aversive effects of smoking via the Modified E-Cigarette Evaluation Questionnaire (MCEQ).Confidence and perceived importance of quitting smoking.

02

Conditions studied

  • Smoking Cessation
  • Motivational Intervention

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Keywords

  • Modified Motivational Interviewing
  • Smoking Cessation
  • Motivational Interviewing
03

In context

Smoking Cessation

304 studies on the registry are indexed under Smoking Cessation; 139 are open to participants now.

This study's enrollment of 200 is above the median of 153 across 285 interventional studies indexed under Smoking Cessation.

Browse Smoking Cessation studies →

Lead sponsor

This is the only study on the registry with Mohammed Al-Hammouri as lead sponsor.

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

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Academic Enrollment: Must be an actively enrolled student at Jordan University of Science and Technology.

Active Smoking Status: Must be an active smoker.

Smoking History: Defined as a person who has smoked more than 100 cigarettes in their life and still currently smokes.

Exclusion criteria

Exclusion Criteria:

Prior Intervention Experience: Having previous experience with Motivational Interviewing (MI).

Prior MMI Exposure: Having previous experience with Modified Motivational Interviewing (MMI).

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Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
200 participants (actual)

Study arms

  • Experimental
    Intervention Group

    Participants who receive the Modified Motivational Interviewing

    Behavioral: Modified Motivational Interviewing

  • No intervention
    Control Group

    Participants who receive no intervention during the active study period but are monitored simultaneously with the intervention group.

Interventions

  • BehavioralModified Motivational Interviewing

    The Modified Motivational Interviewing (MMI) intervention is a self-administered, video-based program that replaces traditional, costly practitioner-led counseling. Distinguishing Features: Participant-Led "Change Talk": Students record 15-minute videos on their mobile devices focusing on four categories: advantages of quitting, optimism for change, intention to change, and status quo disadvantages. Asynchronous Feedback: Researchers provide individualized content feedback, ensuring each video meets behavioral criteria before the next is recorded. Tapered Schedule: To foster independence, frequency decreases over 8 weeks: 2 videos/week (weeks 1-2), 1 video/week (weeks 3-4), and 1 video every 2 weeks (weeks 5-8).Peer Support: Includes an optional private virtual thread for participants to share videos with others in the intervention arm.

06

What researchers measure

Primary outcomes

  1. Physical Dependence on Nicotine

    Fagerstrom Test for Nicotine Dependence (FTND): A 6-item scale resulting in a total score of 0-10, used to categorize dependence from "very low" to "high". with the higher score indicating more nicotine dependency

    Time frame: Baseline, Post-intervention (8 weeks), and 3-month follow-up.

  2. Readiness to Quit Smoking

    Readiness to change Questionnaire Treatment version (RCQ-TV): A 10-point visual analog scale (1 to 10) where higher scores indicate a greater readiness to consider or maintain smoking cessation.

    Time frame: Baseline, Post-intervention (8 weeks), and 3-month follow-up.

  3. Motivation to Quit Smoking

    Smoking Cessation Motivation (QMAT): A 6-item instrument measuring self-efficacy for smoking cessation on a scale of 0 to 24; higher scores indicate higher motivation and self-efficacy.

    Time frame: Baseline, Post-intervention (8 weeks), and 3-month follow-up.

Secondary outcomes

  1. Reinforcing and Aversive Effects of Smoking

    Modified Cigarette Evaluation Questionnaire (MCEQ-11): A self-administered questionnaire assessing five subscales: Satisfaction, Psychological Reward, Enjoyment of Respiratory Tract Sensations, Craving Reduction, and Aversion. Items are scored on a 7-point Likert-like scale. The items in this measure can be answered on a Likert-like scale response options ranging from 0 (Not at all) to 6 (Extremely). The total score is calculated by summing the four subscales, with higher scores indicating greater reinforcing and aversive

    Time frame: Baseline, Post-intervention (8 weeks), and 3-month follow-up.

  2. Importance of Quitting Smoking

    A ruler-based question asking, "How important is it to quit smoking?" with answers ranging from 1 (no importance) to 10 (maximum importance). with higher scores indicating higher Importance.

    Time frame: Baseline, Post-intervention (8 weeks), and 3-month follow-up.

  3. Confidence in Quitting Smoking

    A ruler-based question asking, "How confident do you feel succeeding at quitting smoking?" with answers ranging from 1 (no confidence) to 10 (maximum confidence). with higher scores indicating higher confidence

    Time frame: Baseline, Post-intervention (8 weeks), and 3-month follow-up

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Study locations

1 site
  • Jordan University of Science and Technology
    Irbid, 21110, Jordan
08

References and documents

Study documents

  • Protocol and statistical analysis plan · May 5, 2026

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No — While the proposal does not explicitly state a plan to share IPD with external researchers, it outlines strict data security protocols that suggest access is restricted to the immediate study team: Restricted Access: The proposal states that identifiable data of the participants will be secured and only accessed by the research team. Safety Measures: Further measures will be taken to ensure the safety of participants' data, including the use of informed consent forms before the study begins. Institutional Ownership: According to the Intellectual Property Rights Form of Jordan University of Science and Technology, all research results and products are the property of the university. Confidentiality: Investigators and students are required to maintain full confidentiality regarding any inventions or discoveries resulting from the research.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07577167
Lead sponsor
Mohammed Al-Hammouri
Collaborators
Jordan University of Science and Technology
Responsible party
Mohammed Al-Hammouri (Professor, King Abdullah University Hospital) — Sponsor-investigator
First posted
May 11, 2026
Start date
May 1, 2025
Primary completion
Jan 11, 2026
Completion
Jan 11, 2026
Last update
May 11, 2026

Oversight

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

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