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Comparison of The Effects of Aromatherapy with Lavender Essence Oil and Lavender Tea on Pain, Sleep Quality and Fatigue

Comparison of The Effects of Aromatherapy with Lavender Essence Oil and Lavender Tea on Pain, Fatigue and Sleep Quality in Hemodialysis Patients: A Controlled Clinical Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190531043778N2
Enrollment
90
Registered
2021-04-13
Start date
2021-05-05
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

Hemodialysis. Dependence on renal dialysis

Interventions

Intervention 1: Intervention group: First: Inhalation of lavender with a concentration of 10% for six times in two weeks, each time 5 drops of lavender extract prepared from Barich Essential Oil Compa

Sponsors

Khalkhal University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Perform permanent hemodialysis Have a history of hemodialysis for at least six months Age group 18 to 65 years Ability to communicate Lack of allergy to the smell of plant extracts Absence of respiratory diseases such as asthma, having a healthy sense of smell (through patient statements and nasal examination for non-obstruction) Kidney transplant candidate Non-pregnancy (for women) No addiction Not receiving painkillers, hypnotics and sedatives in the last 3 hours

Exclusion criteria

Exclusion criteria: Lack of interest in participating in the study

Design outcomes

Primary

MeasureTime frame
Score of Pain. Timepoint: At the beginning of the study (before the intervention) and 14 days after the start of intervention. Method of measurement: Visual Analogue Scale questionnaire.;Score of Fatigue. Timepoint: At the beginning of the study (before the intervention) and 14 days after the start of intervention. Method of measurement: Scale Severity Fatigue questionnaire.;Score of Sleep Quality. Timepoint: At the beginning of the study (before the intervention) and 14 days after the start of intervention. Method of measurement: Pittsburgh sleep quality index questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKhadijeh Nasiri

Khalkhal University of Medical Sciences

khadije.nasiri@yahoo.com+98 45 3243 2002

Outcome results

None listed

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