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Effect of aromatic massage of lavender and chamomile on anxiety and sleep quality of patients with burns

Effect of aromatic massage of lavender and chamomile on anxiety and sleep quality of patients with burns

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180120038444N1
Enrollment
105
Registered
2018-01-27
Start date
2018-03-10
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

Burn.

Interventions

Intervention group: Intervention group: Under massage with aromatic chamomile and lavender oil (2 drops of pure lavender essential oil and 2 drops of pure chamomile essential oil, prepared from yellow
Treatment - Other

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 18 years Awareness of time and place Ability to speak and understand Persian language Percentage of burns between 10-45% recorded in the file Skin healthy areas of the leg or back Lack of septicemia symptoms with regard to file information 72 hours after burn Lack of physical disability Degree 2 and 3 burns recorded in the case Lack of mental disorder present and past recorded in the case No history of asthma and allergies to plants No history of blood pressure and migraine recorded in the file Absence of self-immolation Lack of pregnancy

Exclusion criteria

Exclusion criteria: The sample's reluctance to continue cooperation Sepsis in the study Removal of the skin in healthy areas of the leg or back during the intervention Sensitivity to massage oils used during the study Patient's death

Design outcomes

Primary

MeasureTime frame
"The effect of aromatic massage with aromatic oil of lavender and chamomile on reducing anxiety and improving the quality of sleep in patients with burns", the primary outcome is the anxiety score in the Spielberger questionnaire and Pittsburgh Sleep Quality Score. Timepoint: Anxiety and quality of sleep are performed at the beginning of the study (before the intervention) and three days later (end of the intervention). Method of measurement: spielberger's anxiety scale, Pittsburgh Sleep Quality scale.

Secondary

MeasureTime frame
Heart rate and respiratory rate. Timepoint: Measurement of respiratory rate and heart rate in the first day (before and after intervention), second (before and after intervention) and third (before and after intervention). Method of measurement: Heart rate with digital pulse oximeter and manual breathing rate with clock aid.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarzaneh Ameri

Iran University of Medical Sciences

Ameri.f@tak.iums.ac.ir+98 21 4365 1000

Outcome results

None listed

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