Not yet recruiting NCT07202806
A Study on the Application of Aromatherapy Combined With Transcranial Magnetic Stimulation in Insomnia of Stroke Patients
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Aromatherapy.
- Who it may be relevant to
- Registry conditions: Stroke. Basic parameters: 24 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
Exploring the application efficacy of aromatherapy combined with transcranial magnetic stimulation on insomnia in patients with cerebral stroke
Interventions
- Behavioral Aromatherapy
1.Aromatherapy is made from self-made sachet of traditional Chinese medicine.Its components (albizzia, Angelica dahurica, cardamom, Polygala, Evodia, Magnolia, Acorus calamus) are 10g each. Place the pillow 1 hour in advance. It is forbidden to play with your mobile phone or turn off the lights before going to bed.
Primary outcome measures
- Respiratory sleep monitoring [Time frame: From enrollment to the end of treatment for 3 weeks]
Secondary outcome measures (1)
- Pittsburgh sleep quality index,PSQI [Time frame: From enrollment to the end of treatment for 3 weeks]
Eligibility criteria
Inclusion criteria
- Clinical diagnosis of stroke
- Insomnia patients
- Sign the informed consent form, cooperate voluntarily
- Accord with the diagnosis of "insomnia" in traditional Chinese medicine
- Evaluation has no taboo on transcranial magnetism
- The age range is between 24 and 65
Exclusion criteria
- Disturbance of consciousness
- Cognitive impairment
- Mental abnormality
- Sleep apnea syndrome
- Restless leg syndrome
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Quadruple blind
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07202806 · 2024B1366