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Evidence-Based Supplement Research
Evidence-Based Supplement Research

The efficacy of lavender oil on fatigue and sleep quality in patients with hematological malignancy receiving chemotherapy: a single-blind randomized controlled trial.

  • 2025-01-08
  • Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer 33(2)
    • Dilek Yildirim
    • Merve Harman Ozdogan
    • Seckin Erdal
    • Sevinc Selcuk
    • Azize Guneri
    • Elif Begum Simsek
    • Taha Berkay Can
    • Hazal Gunduz
    • Aysem Kuni

Study Design

Type
Randomized Controlled Trial (RCT)
Sample size
n = 120
Population
120 patients with hematological malignancies undergoing chemotherapy
Methods
Randomized, parallel-group study; lavender essential oil applied for 20 min before bed every night for 5 consecutive days; control group received physiological saline solution
Blinding
Open-label
Duration
5 consecutive days
Funding
Unclear
  • Large Human Trial

Purpose

The aim of this study is to evaluate how aromatherapy with the inhalation of lavender oil affects fatigue and sleep quality in patients with hematological malignancies undergoing chemotherapy.

Methods

This randomized, parallel-group study was carried out in the Adult Bone Marrow Transplant unit and Hematology-Oncology clinics between January 2022 and April 2023. A total of 120 patients were assigned to experimental and control groups by randomization. The study was completed with 100 patients including 50 in the experimental group and 50 in the control group. Lavender essential oil was applied to the experimental group for 20 min prior to going to bed every night for 5 consecutive days. Physiological saline solution was applied to the control group in the same way. A Participant Information Form, the Richards-Campbell Sleep Questionnaire, and the Piper Fatigue Scale were used as data collection tools.

Results

The experimental group showed a significantly higher sleep quality (p = 0.001) and had a significantly lower PFS scores (p = 0.001) compared to the control group. Also, the mean scores of the experimental group on the Behavioral, Sensory, and Cognitive subscales were statistically significantly lower than the scores of the control group (p < 0.05). Variables of lavender aromatherapy and total sleep quality accounted for 17.1% of the variance in fatigue levels (R2 = 0.171).

Conclusions

Consequently, it was determined that aromatherapy with lavender essential oil significantly alleviated fatigue and lowered PFS total and subscale scores in patients with hematological malignancies undergoing chemotherapy. Also, sleep quality significantly enhanced in the overall PFS and its subscales.

Trial registration

NCT05808296. Date of Registration: 30 March 2023.

Research Insights

  • The experimental group showed a significantly higher sleep quality (p = 0.001) compared to the control group.

    Effect
    Beneficial
    Effect size
    Moderate
    Dose
    not stated (applied for 20 min prior to bed for 5 consecutive days)
  • the mean scores of the experimental group on the Behavioral, Sensory, and Cognitive subscales were statistically significantly lower than the scores of the control group (p < 0.05).

    Effect
    Beneficial
    Effect size
    Moderate
    Dose
    not stated (applied for 20 min prior to bed for 5 consecutive days)
  • the mean scores of the experimental group on the Behavioral, Sensory, and Cognitive subscales were statistically significantly lower than the scores of the control group (p < 0.05).

    Effect
    Beneficial
    Effect size
    Moderate
    Dose
    not stated (applied for 20 min prior to bed for 5 consecutive days)
  • The experimental group showed a significantly lower PFS scores (p = 0.001) compared to the control group.

    Effect
    Beneficial
    Effect size
    Moderate
    Dose
    not stated (applied for 20 min prior to bed for 5 consecutive days)
  • the mean scores of the experimental group on the Behavioral, Sensory, and Cognitive subscales were statistically significantly lower than the scores of the control group (p < 0.05).

    Effect
    Beneficial
    Effect size
    Moderate
    Dose
    not stated (applied for 20 min prior to bed for 5 consecutive days)
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