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Melissa Officinalis effect on sleep quality and anxiety in patients with acute coronary syndrome

Not Applicable
Conditions
Acute coronary syndrome.
Acute ischaemic heart disease, unspecified
Registration Number
IRCT2017070234851N1
Lead Sponsor
Shahed University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
72
Inclusion Criteria

Entry criteria: company in the study; patients tend to benefit from mental health; not having the experience of sleep disorder before bed; having full consciousness and able to communicate; having no history of chronic pain; addiction to alcohol and drugs; having at least 30 years of age up to 80; the first patient to be hospitalized; the ability to turn taking medication orally; the history of Sleep apnea and COPD; while according to the rating criteria for differentiating diagnosis of Pittsburgh sleep disorder questionnaire before bed with sleep disturbances caused by the patient's hospitalization if you get 0-4 points will be studied; the history of PCI. Exit criteria: cancel the patient's continued cooperation; the patient's feet

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sleep quality. Timepoint: before intervention- at the end of intervention. Method of measurement: Richards-Campbell Sleep Questionnaire (RCSQ).;Anxiety. Timepoint: before intervention- at the end of intervention. Method of measurement: Spielberger State-Trait Anxiety Inventory (STAI).
Secondary Outcome Measures
NameTimeMethod
The side effects of medication. Timepoint: before intervention- at the end of intervention. Method of measurement: Side effects form of medication.
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