The Effect of Lavender Aromatherapy on Cognitive Function in Older Adults With Mild Cognitive Impairment
1 other identifier
interventional
70
0 countries
N/A
Brief Summary
- 1.To analyze the therapeutic effects of lavender aromatherapy on memory function and overall cognitive function in older adults with Mild Cognitive Impairment (MCI);
- 2.To analyze whether lavender aromatherapy improves executive function, language ability, attention, visuospatial ability, anxiety, depression, quality of life, and sleep in older adults with MCI.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Sep 2026
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 2, 2026
CompletedFirst Posted
Study publicly available on registry
July 7, 2026
CompletedStudy Start
First participant enrolled
September 1, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2027
Study Completion
Last participant's last visit for all outcomes
January 2, 2027
July 7, 2026
July 1, 2026
4 months
July 2, 2026
July 2, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Gobal cognitive function
Use the Mini-Mental State Examination to assess overall cognitive function.
Week 12
Memory
Use the Auditory Verbal Learning Test to assess memory function.
Week 12
Secondary Outcomes (8)
Language function
Week 12
Executive function
Week 12
Visual space
Week 12
Attention
Week 12
Anxiety
Week 12
- +3 more secondary outcomes
Study Arms (2)
Aromatherapy experimental group
OTHERAromatherapy experimental group : Aromatherapy The aromatherapy intervention protocol is as follows: Based on the elderly participant's usual bedtime, record the time they go to bed; instruct them to assume a comfortable sleeping position; using the graduated dropper provided with the essential oil bottle, dispense 0.15 ml (approximately 3 drops; theoretically, 0.05 ml per drop) of diluted lavender essential oil and drip it vertically onto the upper center of a cotton pad; pin the cotton pad to the collar with a safety pin; and have the participant inhale the scent evenly for 30 minutes. Afterward, the intervention staff or caregiver will remove the cotton pad. The intervention will be conducted 5 days a week for 12 weeks.
Control group
NO INTERVENTIONno-treatment control group receiving routine health education only
Interventions
Participants in the intervention group will receive aromatherapy inhalation for 30 minutes per session, five times a week, over a period of 12 week
Eligibility Criteria
You may qualify if:
- The MCI mentioned in this study meets the diagnostic criteria proposed by the \*Chinese Expert Consensus on the Diagnosis and Treatment of Alzheimer's Disease-Derived Mild Cognitive Impairment (2021)\*: cognitive impairment reported by the patient or an informant, or identified by an experienced clinician; objective evidence of impairment in one or more cognitive domains, with episodic memory impairment being the most common; complex instrumental activities of daily living may be mildly impaired, but the ability to perform basic activities of daily living remains independent; the diagnostic criteria for dementia are not met.
- MoCA-Beijing version scores were adjusted for education level: ≤13 for junior high school education or below, ≤19 for high school education, and ≤24 for university education or above; MMSE score \>24; ADL score \<23.
- Age between 60 and 79 years.
- Normal olfactory function assessed using the "Sniffin' Sticks" test.
- Ability to communicate normally and complete cognitive assessments.
- Residing in a senior care facility with no plans to leave within the next 12 weeks.
You may not qualify if:
- Presence of other conditions known to affect cognitive function, such as psychiatric disorders (e.g., schizophrenia, depression).
- History of asthma or any allergic conditions.
- Use of any prescription medications that may impact cognitive function (including psychotropic drugs and others)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Yuxin Zhang, Graduate
China Medical University, China
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Student
Study Record Dates
First Submitted
July 2, 2026
First Posted
July 7, 2026
Study Start (Estimated)
September 1, 2026
Primary Completion (Estimated)
January 1, 2027
Study Completion (Estimated)
January 2, 2027
Last Updated
July 7, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share