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Comparison of Citrus Aurantium Aroma and Acupressure on sleep quality in patients undergoing percutaneous coronary intervention (PCI)

Comparison of Citrus Aurantium Aroma and Acupressure on sleep quality in patients undergoing percutaneous coronary intervention (PCI)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201707248665N6
Enrollment
75
Registered
2017-08-14
Start date
2017-08-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Heart disease. Ischemic Heart Disease

Interventions

Intervention 1: In the first group (Citrus Aurantium Aroma) after getting informed consent, they will complete demographic and spielberger questionnaires at 10 o'clock. Cotton is stained with 2 drops
In the first group (Citrus Aurantium Aroma) after getting informed consent, they will complete demographic and spielberger questionnaires at 10 o'clock. Cotton is stained with 2 drops of Citrus Aurant
In the second group (placebo aroma) after getting informed consent, they will complete demographic and Spielberger questionnaire at 10 o'clock. Cotton is stained with 2 drops of sunflower oil put in f
In the third group (Accupressure) after getting informed consent, they will complete demographic and spielberger questionnaires at 10 o'clock. The wristband, which has a metal button with a diameter o
In the fourth group (Placebo of accupressure) after getting informed consent, they will complete demographic and spielberger questionnaires at 10 o'clock. The wristband on both the right and left wris
In the fifth group (Control) after getting informed consent in control group, they will complete demographic and spielberger questionnaires at 10 o'clock. they will receive only routine nursing care.

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Age range 40-75 years; Diagnosis of acute myocardial infarction or angina pectoris requiring PCI; Non-use of herbal medicines in the past two weeks; Not having a history of sleep disorders in a recent month; No- narcotic drug use; no scars at the Shenmen point; Non-use sleep medication during the past month; no history of acupressure; lack of olfactory impairment; patients who are first placed under PCI. Exclusion Criteria: Patient's unwillingness to cooperate or death; History of respiratory disorders or allergies to plants; Carpal tunnel syndrome; BMI> 35.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sleep Quality. Timepoint: At the end of study. Method of measurement: St Marry’s Hospital Sleep questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHassan Babamohamadi

Semnan University of Medical Sciences

babamohamadi@semums.ac.ir+98 23 3365 4190

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 1, 2026