The Effect of Aromatherapy Massage on Sleep Quality

Nilgün Erdoğan

Status: Enrolling

Conditions: Respiratory Failure; Respiratory Disease; Diabetes Mellitus; Pneumonia; Stroke, Ischemic

Treatments: Other: Intervention 1 Group; Other: Intervention 2 Group; Other: Placebo Control Group

Study type: Interventional

Funder types: Other

Identifiers

NCT06295900

19.10.2023/63

Details and patient eligibility

About

Sleep disturbance is one of the most common complaints of patients admitted to ICU. Insufficient sleep in intensive care units may be associated with environmental reasons such as excessive light at night, loud warning sounds and mechanical ventilation alarms, as well as non-environmental factors, including the situation at the time of admission. Sleep assessment is subjective in nature, so it is difficult to perform in the ICU. Since communication with the patient is prevented, clear information about perceived rest and disturbing factors cannot be provided. For this reason, night rest is an issue that is often forgotten and ignored. This study applied a mixture of lavender, medicinal chamomile and neroli oil (in 20 ml of sweet almond oil; lavender oil 2 drops, medicinal chamomile 4 drops, neroli oil 6 drops) to patients who were monitored in intensive care on high-flow and oxygen, once a day for three days. This study will be conducted to determine the effect of aromatherapy massage applied for a total of 30 minutes on sleep quality.

Enrollment: 62 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 18 years of age and over,
• Conscious patients,
• Staying in intensive care for 24 hours or more,
• Those with stable hemodynamic status,
• Receiving O2 therapy,
• Intubated patients, patients who have passed 24 hours after being extubated,
• Those whose saturation level is 85 and above

Exclusion criteria

• Patients with peripheral neuropathy or quadriplegia,
• Patients with open wounds on their body,
• Patients receiving analgesia and sedation infusion,
• Patients who are sedated,
• Patients in delirium,
• Patients with allergies detected before starting the application

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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62 participants in 3 patient groups, including a placebo group

Intervention 1 Group

Active Comparator group

Description:

In this group, application is made with chamomile, lavender and neroli oil.

Treatment:

Other: Intervention 1 Group

Intervention 2 Group

Sham Comparator group

Description:

In this group, application is made with lavender oil.

Treatment:

Other: Intervention 2 Group

Placebo Control Group

Placebo Comparator group

Description:

In this group, application is made only with almond oil.

Treatment:

Other: Placebo Control Group