Circuit Breathing Exercise on Smoking Cessation Among Youth E-Cigarette Users
Acute Effects of Circuit Breathing Exercise on Smoking Cessation and Respiratory Function Among Youth E-Cigarette Users
1 other identifier
interventional
20
1 country
1
Brief Summary
This study aims to investigate the acute effects of a circuit breathing intervention on nicotine withdrawal symptoms and respiratory parameters among youth who use e-cigarettes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Aug 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 15, 2026
CompletedFirst Submitted
Initial submission to the registry
October 10, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 15, 2026
CompletedFirst Posted
Study publicly available on registry
October 21, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
October 30, 2026
ExpectedOctober 21, 2026
October 1, 2026
2 months
October 10, 2026
October 16, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
E-cigarette Dependence
E-cigarette dependence will be assessed using the Penn State Electronic Cigarette Dependence Index, adapted by Sornsenee et al. (2025). The questionnaire consists of 10 items, with a maximum total score of 20. Scores are interpreted as follows: 0-3 indicates no e-cigarette dependence, 4-8 indicates low dependence, 9-12 indicates moderate dependence, and 13 or higher indicates high dependence.
Baseline for demographic data.
Nicotine Withdrawal Symptoms
Nicotine withdrawal symptoms will be assessed using the Thai version of the Minnesota Nicotine Withdrawal Scale-Revised (MNWS) (Hughes \& Hatsukami, 2008), translated by Sirirat Kanokururot and Sunida Preechawong (2010). This self-report questionnaire measures the perceived severity of nicotine withdrawal symptoms. It consists of 9 items rated on a 5-point scale ranging from 0 (no symptoms) to 4 (severe symptoms). The total score ranges from 0 to 36, with a score of 0 indicating no nicotine withdrawal symptoms and a score of 36 indicating the most severe nicotine withdrawal symptoms.
Immediately before and immediately after each breathing intervention session.
Secondary Outcomes (2)
Fractional Exhaled Nitric Oxide (FeNO)
Immediately before and immediately after each breathing intervention session.
Peak Nasal Inspiratory Flow (PNIF)
Immediately before and immediately after each breathing intervention session.
Study Arms (3)
Circuit Breathing
EXPERIMENTALDiaphragmatic Breathing
EXPERIMENTALNormal Breathing
EXPERIMENTALInterventions
The circuit breathing intervention consists of five stations: paper suction using a straw, blowing a toy pinwheel, incentive spirometry, balloon blowing, and weighted diaphragmatic breathing. Participants will rest for 1 minute between stations.
The diaphragmatic breathing exercise will consist of inhaling through the nose for 4 seconds and exhaling through the nose for 6 seconds, continuously for 10 minutes per set. Participants will rest for 1 minute between sets and complete a total of 3 sets.
Participants will breathe normally through the nose without deliberately controlling the rate, rhythm, or depth of breathing. Breathing will remain at each participant's natural pace for approximately 30 minutes.
Eligibility Criteria
You may qualify if:
- Male or female aged 15-25 years.
- Regular e-cigarette use for at least six months and current e-cigarette use, defined as use on at least one day per week or at least 10 puffs per day during the past 30 days.
- Not regularly physically active, defined as exercising fewer than two times per week during the preceding six months.
- Able to understand instructions, communicate effectively, and cooperate with the research procedures.
- No history of cardiovascular disease or respiratory disease, such as asthma or chronic obstructive pulmonary disease.
- No uncontrolled hypertension. Participants with controlled hypertension must have resting blood pressure ≤140/90 mmHg.
- Able to move independently without assistance or assistive devices.
- Willing to participate and provide informed consent.
- For participants younger than 18 years, consent from a parent or legally authorized representative is required.
You may not qualify if:
- Development of an illness, injury, or other circumstance that prevents continued participation.
- Withdrawal of consent or unwillingness to continue participation.
- Current use of illicit drugs or other tobacco/nicotine products, including conventional cigarettes, shisha/hookah, roll-your-own tobacco, or other nicotine-containing products.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Faculty of Sports Science, Chulalongkorn University
Bangkok, Bangkok, 10330, Thailand
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal investigator
Study Record Dates
First Submitted
October 10, 2026
First Posted
October 21, 2026
Study Start
August 15, 2026
Primary Completion
October 15, 2026
Study Completion (Estimated)
October 30, 2026
Last Updated
October 21, 2026
Record last verified: 2026-10
Data Sharing
- IPD Sharing
- Will not share