Actively Recruiting

Phase Not Applicable
All Genders
NCT07192783

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

Led by Ardahan University · Updated on 2025-09-25

50

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is 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.

CONDITIONS

Official Title

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

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with primary hypertension
  • Willing to participate in the study
  • No allergy to lavender
  • No olfactory impairments
  • No history of psychiatric disorders
Not Eligible

You will not qualify if you...

  • 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

AI-Screening

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Trial Site Locations

Total: 1 location

1

Ardahan State Hospital

Ardahan, Ardahan, Turkey (Türkiye), 75000

Actively Recruiting

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Research Team

D

Derya ŞİMŞEKLİ, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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