"The effect of acupressure with valerian Oil 2/5% on Quality and Quantity of sleep of patients with Acute coronary Syndrome (ACS)"

"The effect of acupressure with valerian Oil2/5% on Quality and Quantity of sleep of patients with Acute coronary Syndrome ( ACS)"

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT201302277494N3

Enrollment

Registered

2013-08-11

Start date

2013-03-07

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

Sleep. Nonorganic disorder of the sleep-wake schedule

Interventions

Intervention 1: Intervention in first group( Valerian acupressure):Intervention in Acupressure with valerian oil's group such manner that this patient will received acupoint massage Second night in h

Intervention in first group( Valerian acupressure):Intervention in Acupressure with valerian oil's group such manner that this patient will received acupoint massage Second night in hospitalization,

Intervention in third group( control): The control group every night between 7 to 10 PM will received shame acupoint massage(1-1/5 Centimeter from true acupoint) in Respectively in Feng Chi(GB20) behi

Intervention in second group ( acupressure): Acupressure's group will received acupoint massage from Second night in hospitalization, the top of the head Respectively in Feng Chi(GB20) behind the head

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: The main inclusion criteria is at least eighteen years of age; being aware of the time and place of not surgery; EF is above 40%. The main exclusion criteria in this study received the opioid drug five or six hours of sleep the night before; despite hearing and vision impairments (such as not being able to communicate with the investigator if); have addiction to drug; have an allergy to plants and flowersand; habit to use of any matter or procedure affecting the sleep; using inotropes drugs; leg amputation or ulcer at the site of acupoints; acute problems at admission and continuing to investigate the individual does not cooperate.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Quality. Timepoint: Before the study -The first to the fourth day of hospitalization. Method of measurement: SMHSQ.	—

Secondary

Measure	Time frame
Quantity of sleep. Timepoint: Baseline and every day until the fourth day. Method of measurement: Sleep Log.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mohammad Ali Heydari Gorgi

Mazandaran University of Medical Science

heydarigorji@yahoo.com+98 15 1226 7342

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026