Aromatherapy massage to improve sleep quality in ICU patients
The Effect of Aromatherapy Massage Applied to Intensive Care Patients on Sleep Quality
This study tests if aromatherapy massage with lavender and other oils can help improve sleep quality for patients in the ICU.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 62 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Nigde Omer Halisdemir University Academic / other |
| Locations | 1 site (Nigde) |
| Trial ID | NCT06295900 on ClinicalTrials.gov |
What this trial studies
This study investigates the impact of aromatherapy massage using a blend of lavender, medicinal chamomile, and neroli oil on the sleep quality of patients in intensive care units. The intervention involves applying the aromatherapy mixture to conscious patients who have been in the ICU for at least 24 hours and are receiving oxygen therapy. The treatment is administered once daily for three days to assess its effectiveness in enhancing sleep quality amidst the challenging ICU environment. The study aims to provide insights into non-pharmacological methods to improve rest for critically ill patients.
Who should consider this trial
Good fit: Ideal candidates include conscious adults over 18 years old who have been in the ICU for at least 24 hours and are receiving oxygen therapy.
Not a fit: Patients with conditions such as peripheral neuropathy, quadriplegia, or those who are sedated or in delirium may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance sleep quality for patients in intensive care, leading to better recovery outcomes.
How similar studies have performed: While the use of aromatherapy in clinical settings is gaining interest, this specific approach in the ICU context is relatively novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Nigde
- Ömer Halisdemir University Training and Research Hospital — Nigde, Turkey (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.