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NCT Number: NCT07732179

Aromatherapy and Music Impact on Nurses' Stress at Work

The purpose of the Doctor of Nursing Practice research project is to determine if nurses who receive chamomile-lavender aromatherapy and listen to music during a 20-minute break once per shift for 8 weeks, will experience report decreased work stress (measured by self-reported symptoms of anxiety) compared to before the aromatherapy and music intervention during breaks.

The investigators know nurses are at high risk for stress and anxiety. Despite the current processes and policies in place at Northwestern Memorial Hospital that support nurses to take breaks during their shifts, nurses continue to share feeling stressed and anxious. Included in this Doctor of Nursing Practice research project is an evidence synthesis of fourteen studies supporting the idea that combining aromatherapy and music can reduce anxiety in both adults and children.

The evidence-based intervention being studied is administering lavender-chamomile essential oil aromatherapy and listening to music during 20-minute non-meal breaks once a shift for 8 weeks. Participants will go to a quiet breakroom, pour 3 drops of lavender-chamomile essential oil onto a non-adhesive 2X2 gauze pad, and place the pad about 20 centimeters from their noses while also listening to their preferred calming music through their personal phones and wireless earbuds or headphones for twenty minutes.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Northwestern Medicine Academic Medical Center

Chicago, Illinois, 60611, United States

Location status: Recruiting

Location contact

Angela Maeder, PhD, RNC-OB

CONTACT

[email protected]

3129269258

Angela Maeder, PhD, RNC-OB

PRINCIPAL_INVESTIGATOR

Sarah Buenaventura, MSN, RN, NE-BC

CONTACT

[email protected]

3129261061

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

-CCU nurses at NM AMC providing direct patient care.

Exclusion criteria

  • not currently pregnant
  • no allergies to essential oils.

Treatment and study plan

lavender-chamomile aromatherapy oil and music

Other

There is only one experimental arm in this study. All participants will self-administer aromatherapy oil while listening to music during their scheduled 20-minute rest break during work hours.

Primary outcomes

  1. Measure of workplace stress

    Time frame: The Beck Anxiety Inventory will be given before the intervention begins. After the 10 week intervention period, the participants will be asked to complete the Beck Anxiety Inventory again as a post-intervention measure.

    The Beck Anxiety Inventory will be used to measure workplace stress. Scores on this tool range from a total of 0 to 63. There are 21 items and each item can receive a score of 0 to 3. Higher scores are associated with higher stress/anxiety.

  2. stress

    Time frame: The intervention time period is 10 weeks.

    The Beck Anxiety Inventory will be used to assess levels of workplace stress before and after this intervention.

Study contacts

Contact information is provided by the study sponsor or research team.

Angela Maeder, PhD, RNC-OB

CONTACT

[email protected]

3129269258

Sarah Buenaventura, MSN, RN, NE-BC

CONTACT

[email protected]

3129261061

Sponsors and collaborators

Lead sponsor

Northwestern University

Other

Collaborators

  • Northwestern Medicine

Registry information

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jul 28, 2026
Registry last updated
Jul 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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