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Jasmine impact on the levels of anxiety and cortisol exposure of patients to the operating room

Comparison the effect of inhalation of essential oils of jasmine with distilled water on the level of anxiety and blood cortisol of patients before laparotomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015072510325N4
Enrollment
84
Registered
2015-09-24
Start date
2015-07-26
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Anxiety. Generalized anxiety disorder.

Interventions

Control group: inhale two drops of distilled water as a placebo for 60 minutes on the patient's shirt collar shed. Intervention will be held the morning of surgery.
Intervention 1: Group intervention:The subjects inhale two drops of essential oil of Jasmine Barij Essence Kashan product for 60 minutes. Jasmine will be dropped on the patient's shirt collar shed. Th
Placebo
Group intervention:The subjects inhale two drops of essential oil of Jasmine Barij Essence Kashan product for 60 minutes. Jasmine will be dropped on the patient's shirt collar shed. The surgery will b

Sponsors

Golestan University of Medical Sciences Vice Chancellor for research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 65-15 years old, patients who are candidate for laparotomy without a history of mental illness and no signs of trauma to the brain, alert to place, time and self orientation, no history of allergy to plants, no disorder in smell, having ability to read and response to questionnaire items, no history of using steroid during 3 months ago, or those disease that increase the level of blood Cortisol. Exclusion criteria: Patient's intolerance due to Jasmine extraction, patient transmission before the intervention, the patient withdraw from the study, and the patients with anxiety or depression disorders.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
??Anxiety. Timepoint: Before and one hour (60 minutes) after intervention the anxiety will be measured. Method of measurement: Spielberger questionnaire.;Blood Cortisol. Timepoint: Before and one hour after intervention the subjects' blood samples will be taken and the level of Cortisol will be measured. Method of measurement: Using ELISA monitors Cortisol IBl kit.

Secondary

MeasureTime frame
Vital sign. Timepoint: Before and one hour after intervention. Method of measurement: Blood pressure of the subjects will be measured before and after the intervention by a Manometer ALPK2 that was manufactured by Japan. The subjects' pulse rate and respiratory rate will be counted.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohamad Yadegari

Golestan University of Medical Sciences.

mahmoodigh@yahoo.commohamad.yadegari970@gmail.com+98 17 3242 6900

Outcome results

None listed

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