Effect of Agarwood (Aquilaria Sinensis) Inhalation Aromatherapy on Workplace Fatigue and Sleep Quality Among Hospital Employees: A Randomized Controlled Trial

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20+
SponsorDa-Yeh University

About this trial

Hospital staff often experience workplace fatigue and poor sleep quality, which can harm their health, reduce job performance, and increase risks to patient safety. Aromatherapy is a simple, non-invasive complementary therapy that may help reduce fatigue and improve sleep. Agarwood (Aquilaria spp.) has calming and relaxing properties, but there is little clinical research on its effectiveness for hospital staff.

This randomized, double-blind, controlled trial will evaluate whether agarwood aromatherapy inhalation can improve fatigue and sleep quality among hospital employees in Taiwan. About 78 participants will be recruited and randomly assigned to one of two groups:

1. Experimental group: Agarwood sachet containing agarwood wood chips and essential oil. 2. Control group: Placebo sachet containing almond oil.

Participants will place the sachet about 60 cm from the nose during sleep for 7 nights. Data will be collected using questionnaires on workplace fatigue and sleep quality (Pittsburgh Sleep Quality Index, PSQI). The main questions this study aims to answer are: 1. Does agarwood aromatherapy reduce workplace fatigue in hospital staff? 2. Does agarwood aromatherapy improve sleep quality compared with placebo?

Findings are expected to provide scientific evidence for using agarwood inhalation as a safe and convenient strategy to improve staff well-being and support a healthier hospital environment.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

≥20 years old, hospital employee working ≥30 hrs/week, employed ≥3 months

Not using sedatives/hypnotics

Normal olfactory function (verified with coffee/vinegar smell test)

Clear consciousness, can read and understand Chinese, no major communication barriers

Disqualifiers

Major psychiatric disorders (e.g., major depression, schizophrenia)

Malignancy under active radio/chemotherapy

CNS diseases (e.g., brain tumor)

History of asthma, fragrance allergy, pregnancy

Trial design

Design model

Parallel

Treatments tested in this trial

  • Agarwood Aromatherapy Inhalation

    Other intervention

    The experimental group will receive agarwood essential oil sachets as the aromatherapy intervention, and participants will place the sachet 60 cm from the nose during sleep for one week.

Treatment groups

78 Participants
are divided into 2 treatment groups
Group A: Group of agarwoodExperimental treatment 1 intervention
Group B: Group of sachetActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Workplace Fatigue

Change in fatigue levels measured by the Chinese version of the Copenhagen Burnout Inventory (21 items across four domains: personal, work-related, client-related, and overcommitment). Higher scores indicate greater fatigue.

Time frame
Baseline and after 1-week intervention

Secondary outcomes

1

Sleep Quality

Change in sleep quality measured by the Pittsburgh Sleep Quality Index (PSQI, 19 items, 7 domains). Total scores range from 0 to 21, with higher scores indicating poorer sleep quality.

Time frame
Baseline and after 1-week intervention

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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