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Clinical Trials/NCT06914167
NCT06914167CompletedNot Applicable

The Effectiveness of Lavender Aromatherapy Combined With Slow Breathing Exercises in Improving Occupational Burnout and Sleep Disorders Among Nursing Staff

Tri-Service General Hospital2 sites in 1 country70 target enrollmentStarted: April 1, 2025Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
70
Locations
2
Primary Endpoint
Nursing Burnout Scale, NBS

Study Overview

Brief Summary

This study investigates the effects of breathing exercises combined with lavender essential oil inhalation on occupational burnout and sleep disturbances in rotating shift nurses.

Detailed Description

This study will adopt a randomized controlled trial (RCT) design targeting rotating shift nurses with at least six months of clinical experience at a regional teaching hospital in northern Taiwan. Eligible participants who consent to join the study will be randomly assigned into five groups using block randomization. The randomization process will be conducted via sealed envelopes to allocate participants into the following groups: Experimental Group 1, Experimental Group 2, Experimental Group 3, Breathing-Only Group, and Control Group.

Experimental Group 1: Participants will receive slow breathing training (6 breaths per minute) once daily before bedtime, combined with the inhalation of 3 drops of natural lavender essential oil on a towel, for 3 minutes, over a 4-week period.

Experimental Group 2: Same breathing protocol as above, with 3 drops of linalyl acetate-containing essential oil.

Experimental Group 3: Same breathing protocol, with 3 drops of linalool-containing essential oil.

Breathing-Only Group: Participants will perform slow breathing training (6 breaths per minute) for 3 minutes daily before bedtime, without any essential oil inhalation, for 4 weeks.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Double (Participant, Care Provider)

Eligibility Criteria

Ages
20 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Aged between 20 and 65 years Registered nurses with at least 6 months of clinical experience and currently working rotating shifts Scores ≥1 in each of the three dimensions (emotional exhaustion, reduced personal accomplishment, depersonalization) on the Nursing Burnout Scale (NBS) Willing to participate in the study and accept random assignment

Exclusion Criteria

  • Nurses with less than 6 months of clinical experience Individuals with anosmia or reduced sense of smell Diagnosed with psychiatric disorders Allergic to lavender essential oil Not currently working rotating shifts

Arms & Interventions

Control Group

No Intervention

Participants will maintain their usual lifestyle without any intervention.

Breathing-Only Group

Placebo Comparator

Participants will perform slow breathing training (6 breaths per minute) for 3 minutes daily before bedtime, without any essential oil inhalation, for 4 weeks.

Intervention: Slow Breathing Exercises (Behavioral)

Experimental Group 1

Experimental

Participants will receive slow breathing training (6 breaths per minute) once daily before bedtime, combined with the inhalation of 3 drops of natural lavender essential oil on a towel, for 3 minutes, over a 4-week period.

Intervention: Slow Breathing Exercises (Behavioral)

Experimental Group 1

Experimental

Participants will receive slow breathing training (6 breaths per minute) once daily before bedtime, combined with the inhalation of 3 drops of natural lavender essential oil on a towel, for 3 minutes, over a 4-week period.

Intervention: Lavender Essential Oil Inhalation (Behavioral)

Experimental Group 2

Experimental

Same breathing protocol as above, with 3 drops of linalyl acetate-containing essential oil on a towel, for 3 minutes, over a 4-week period.

Intervention: Slow Breathing Exercises (Behavioral)

Experimental Group 2

Experimental

Same breathing protocol as above, with 3 drops of linalyl acetate-containing essential oil on a towel, for 3 minutes, over a 4-week period.

Intervention: linalyl acetate essential oil Inhalation (Behavioral)

Experimental Group 3

Experimental

Same breathing protocol, with 3 drops of linalool-containing essential oil on a towel, for 3 minutes, over a 4-week period.

Intervention: Slow Breathing Exercises (Behavioral)

Experimental Group 3

Experimental

Same breathing protocol, with 3 drops of linalool-containing essential oil on a towel, for 3 minutes, over a 4-week period.

Intervention: linalool essential oil Inhalation (Behavioral)

Outcomes

Primary Outcomes

Nursing Burnout Scale, NBS

Time Frame: At baseline, and at 4 and 8 weeks following the start of intervention

The Nurse Burnout Inventory is specifically developed based on nurses' clinical practice experiences. It includes items that reflect three key dimensions: emotional exhaustion resulting from the high-tension clinical work environment, reduced personal accomplishment associated with feelings of ineffectiveness in medical care, and depersonalization, characterized by indifference toward others due to prolonged burnout.

Secondary Outcomes

  • The Chinese version of the Pittsburgh Sleep Quality Index, CPSQI(At baseline, and at 4 and 8 weeks following the start of intervention)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Chen, Yao-Hsiang

Assistant hand nurse

Tri-Service General Hospital

Study Sites (2)

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