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Feasibility and efficacy of an aroma therapeutic nurse led intervention to promote sleep in the critically ill – a randomised controlled pilot study

Feasibility and efficacy of an aroma therapeutic nurse led intervention to promote sleep in the critically ill – a randomised controlled pilot study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00012646
Enrollment
60
Registered
2017-07-07
Start date
2018-06-29
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

F51.0 F51.1 F51.2 F51.8 F51.9

Interventions

Group 1: Critically ill patients Once, at night, a warm/humid pad with 5-7 drops of the essential oil of lavender (Lavandula angustifolia) will be applied for 15-20 minutes on the solar plexus of the

Sponsors

Pflegedirektorin, Universitätsklinukum Schleswig-Holstein, Campus Lübeck
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Given consent, at least 1 night at the intensive care unit, no continuous analgesic sedation, no regularly application of benzodiazepines, hypnotics or neuroleptic agents at night. Stay in a single bedroom, sufficient knowledge of German to understand the aim and course of the study, to give consent and to be able to answer the RCSQ).

Exclusion criteria

Exclusion criteria: Sedated (RASS=-4/-5) and delirious patients (CAM –ICU +) will be excluded (the latter assessment are regularly used at the participating icu`s). Furthermore, patients with dementia, bronchial asthma, acute exacerbation of copd and or bronchial hyperreactivity and an insufficient knowledge of the German language. Another exclusion criterion is an allergic reaction of one of the used oils.

Design outcomes

Primary

MeasureTime frame
-Objective Measurement of sleep depth and length using the Bispectral Index (BIS™ 2-Kanal Monitor /Medtronic GmbH) during 11.00-05.00 p.m. -Self-perception of the participant will be assessed the following morning(between 09.00-11.00 a.m.), using the German version of the Richards Campbell Sleep Questionnaire

Secondary

MeasureTime frame
Evaluation of participants in regard of the perceived effectiveness of the intervention, Characteristics, Demographics, Process evaluation

Countries

Germany

Contacts

Public ContactSusanne Krotsetis

Universitätsklinukum Schleswig-Holstein, Campus LübeckPflegeforschung, angegliedert dem Vorstand für Krankenpflege und Patientenservice

susanne.krotsetis@uksh.de0451-50013613

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026