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Clinical Trials/IRCT20220915055965N1
IRCT20220915055965N1
Recruiting
Phase 3

The effect of lavender aromatherapy on anxiety and cognitive status of patients undergoing electroconvulsive therapy in 5 Azargargan hospital in2022

Gorgan University of Medical Sciences0 sites80 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Bipolar disorder.
Sponsor
Gorgan University of Medical Sciences
Enrollment
80
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Gorgan University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • Admitted to the psychiatric department, all patients with ECT indication based on DSM\-5 criteria with the diagnosis of a psychiatrist, consent to participate in the study, the ability to verbally communicate with the researchers, aged 25 to 55 years, patients benefit from minimal reading and writing literacy. (Middle or 8th grade), do not have any disease or physical disability such as speech, hearing or vision impairment, a positive smell test (olfactory nerve health test) is taken from them in such a way that the coffee sample is taken under their nose with their eyes closed and smell it), have no history of physical problems that lead to cognitive disorders such as mental retardation, epilepsy, dementia, and head trauma, no physical diseases related to anxiety and cognitive disorders such as pheochromocytoma, thyroid problems, and brain tumors, no bad Consuming alcohol and drugs, not taking anti\-anxiety drugs, being aware of the time and place before the electroshock, having the physical and mental ability to answer questions, not having a history of allergies and respiratory diseases, schizophrenic patients who are dominated by negative symptoms and their reality check is impaired. are not eligible to enter the study.

Exclusion Criteria

  • Patients who have difficulty communicating verbally, withdraw from the study, have an allergy to lavender during the intervention, decrease the level of consciousness of the patient during the study, participate in other studies that affect their anxiety and cognitive status.

Outcomes

Primary Outcomes

Not specified

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