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Investigating the effect of lavender scent on the side effects of smoking

The effect of lavender aromatherapy on boredom, severity of anxiety, cognitive function, clinical factors in smokers users

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230320057758N1
Enrollment
80
Registered
2023-03-28
Start date
2023-07-21
Completion date
Unknown
Last updated
2023-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nicotine dependence. Nicotine dependence, cigarettes

Interventions

Intervention 1: Intervention group: Intervention group: includes 40 participants. In this group, before the intervention, tests of impatience, anxiety, cognitive function, as well as clinical factors

Sponsors

Kashan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 49 Years

Inclusion criteria

Inclusion criteria: Willingness of participants to enter the experiment Age range 18-49 years Not having a chronic disease, including mental illness or diabetes, blood pressure or heart disease, hepatitis, etc. All people who are smoking or have not quit smoking for a long time and their Fagerstrom score is at least 4.

Exclusion criteria

Exclusion criteria: Unwillingness to participate in the study Taking any kind of drugs Any chronic physical disease that is newly diagnosed and interferes with the test results, including diabetes, high blood pressure, etc.

Design outcomes

Primary

MeasureTime frame
Boredom score of MSBS questionnaire. Timepoint: Completing the questionnaire before the intervention and on the 15th day of the intervention. Method of measurement: MSBS questionnaire.;Expression intensity by Hamilton questionnaire. Timepoint: Completing the questionnaire before the intervention and on the 15th day of the intervention. Method of measurement: Hamilton Anxiety Severity Questionnaire.;Cognitive performance score of MoCA questionnaire. Timepoint: Completing the questionnaire before the intervention and on the 15th day of the intervention. Method of measurement: MoCA Cognitive Function Questionnaire.;Sleep quality score of Petersborg Sleep Disorder Questionnaire. Timepoint: Completing the questionnaire before the intervention and on the 15th day of the intervention. Method of measurement: Petersburg Sleep Disorder Questionnaire.;Blood pressure measurement. Timepoint: Measurement before the intervention and day 15 of the intervention. Method of measurement: Blood pressure measuring device.;Heart rate measurement. Timepoint: Measurement before the intervention and day 15 of the intervention. Method of measurement: Heart rate monitor.;Blood oxygen measurement. Timepoint: Measurement before the intervention and day 15 of the intervention. Method of measurement: Blood oxygen measuring device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmir ghaderi

Kashan University of Medical Sciences

gaderiam@yahoo.com+98 31 3457 4191

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026