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The Effect of Lavender Inhalation on Anxiety, Sleep, and Blood Pressure

A

Ardahan University

Status

Enrolling

Conditions

Primary Hypertension

Treatments

Other: Lavender

Study type

Interventional

Funder types

Other

Identifiers

NCT07192783
ArdahanU-Şimsekli-DS-06

Details and patient eligibility

About

This study aims to determine the effects of lavender oil inhalation on anxiety, sleep quality, and blood pressure in patients with primary hypertension. The study is designed as a double-blind randomized controlled trial. The study population consists of patients presenting to the Cardiology Outpatient Clinic of Ardahan State Hospital. Participants are randomly assigned to an experimental group, which will receive a total of 12 lavender oil inhalations three times a week for one month, or to a control group, which will continue routine treatment and care. Data will be collected using the Hypertension Diagnostic Form, Beck Anxiety Inventory, and Pittsburgh Sleep Quality Index. Statistical analyses will be conducted to compare outcomes between the experimental and control groups.

Full description

This study aims to evaluate the effects of lavender oil inhalation on anxiety, sleep quality, and blood pressure in patients with primary hypertension. It is designed as a double-blind randomized controlled trial. Patients presenting to the Cardiology Outpatient Clinic of Ardahan State Hospital will be recruited for the study. Participants will be randomly assigned to an experimental group, which will receive 12 lavender oil inhalations three times a week for one month, or to a control group, which will continue routine care. Data will be collected using the Hypertension Diagnostic Form, Beck Anxiety Inventory, and Pittsburgh Sleep Quality Index. The study will assess whether lavender oil inhalation affects anxiety, sleep quality, and blood pressure in this population. Statistical analyses will be conducted to compare outcomes between the experimental and control groups.

Enrollment

50 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosed with primary hypertension
  • Willing to participate in the study
  • No allergy to lavender
  • No olfactory impairments
  • No history of psychiatric disorders

Exclusion criteria

  • Communication difficulties
  • Unwilling to participate
  • Using other herbal or aromatherapy treatments
  • History of sleep disorders affecting sleep quality (e.g., obstructive sleep apnea)
  • Secondary hypertension or other chronic diseases
  • Pregnant or breastfeeding
  • Use of tobacco products

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

50 participants in 2 patient groups

experimental group
Experimental group
Description:
Participants receive lavender oil inhalation three times per week for one month (total of 12 sessions) in addition to routine care for primary hypertension. Anxiety, sleep quality, and blood pressure are assessed before and after the intervention.
Treatment:
Other: Lavender
Routine care only
No Intervention group
Description:
Participants in the control group continue their routine care and treatment for primary hypertension without receiving lavender oil inhalation. Anxiety, sleep quality, and blood pressure are assessed before and after the study period.

Trial contacts and locations

1

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Central trial contact

Derya ŞİMŞEKLİ, PhD

Data sourced from clinicaltrials.gov

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