Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID06474793

Aromatherapy Applied to Intensive Care Nurses Effect on Fatigue and Sleep Quality

Led by TC Erciyes University · Updated on 2025-05-22

60

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying the effects of aromatherapy on fatigue and sleep quality among intensive care nurses. This mixed-design study includes both qualitative and quantitative phases to understand how different aromatherapy oils might help reduce fatigue and improve sleep. The research focuses on nurses working in intensive care units who experience moderate to severe fatigue and sleep problems, aiming to evaluate the impact of specific oil mixtures compared to a placebo. The study involves three groups: one receiving a mixture of chamomile and lavender oils, a second using vetiver oil, and a placebo group applying jojoba oil. Participants apply the oils once daily for four weeks, 30 minutes before bedtime, massaging the edges of their nostrils and behind their ears for a total of eight minutes. The qualitative phase includes in-depth interviews with a subset of participants after the treatment period. Participants will be assessed using several tools, including the Visual Analog Scale for fatigue, the Piper Fatigue Scale, and the Pittsburgh Sleep Quality Index, with measurements taken up to three months. Data collection also includes personal information and practice monitoring forms. The study monitors adherence to the oil application process and gathers nurse opinions to understand the therapy's effects. The total participation period includes the four weeks of treatment and follow-up assessments.

CONDITIONS

Brief Title

Aromatherapy Applied to Intensive Care Nurses Effect on Fatigue and Sleep Quality

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Not pregnant
  • Understands and speaks Turkish
  • No hearing or visual impairment
  • Without chronic disease
  • Not allergic to odors
  • Not using sleeping pills
  • Nurses who work the same shifts
  • Will not change the perfume used within a month
  • Complaints of moderate and severe fatigue (VAS fatigue score of 3 or higher)
  • Pittsburgh Sleep Quality Scale score of 5 and above
  • Not diagnosed with psychiatric disease
  • Volunteering to participate in the study
Not Eligible

You will not qualify if you...

  • Allergic to lavender oil
  • Allergic to chamomile oil
  • Disability in smelling
  • On annual leave or sick leave

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 4 weeks

Participants apply aromatherapy oil mixtures by massaging the edges of the nostrils and behind the ears once a day, 30 minutes before going to bed, for four weeks.

Daily self-application at home

Follow-up

Duration - Up to 3 months

Participants are monitored for fatigue and sleep quality for up to 3 months after treatment ends.

Assessments at scheduled intervals during follow-up

Trial Site Locations

Total: 1 location

1

Kayseri City Hospital

Kayseri, Kocasinan, Turkey (Türkiye), 38010

Actively Recruiting

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Research Team

B

BURKEV

F

FATMA GÖNÜL BURKEV

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

Frequently Asked Questions

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