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The survey effect of planned visit on anxiety , depression, sleep and physiological factors of ACS patients in CCU wards of BUMS

The survey effect of planned visit on anxiety , depression, sleep and physiological factors of ACS patients in CCU wards of BUMS ,2012

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201204209521N1
Enrollment
72
Registered
2013-06-02
Start date
2012-09-05
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

Acute coronary syndrom. Ischaemic heart diseases

Interventions

Intervention 1: Planned visiting in case group: tree time visiting with family at second and third day of hospitalizationwith tree persons of patients relative. Intervention 2: In controll groupe dont
Planned visiting in case group: tree time visiting with family at second and third day of hospitalizationwith tree persons of patients relative
In controll groupe dont interfere & patient received routin visiting (one time in day visiting with family in second & third days of hospitalization with open visitores

Sponsors

Nursing faculty, Baqiatallah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patient with acute coronary syndrome; no history of anxiety and depression; age renge in 35 to 55 years old; no history of chronic heart failure and COPD; do not use of cardiac pace maker device and no history of CCU hospitalization. Exclusion criteria: cardiac arrest and CPR; need for use of cardiac pace maker device durig the assessment.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sleep. Timepoint: First, second and third day of hospitalization,. Method of measurement: Questionnaire.;Hospital depression. Timepoint: First and third days of hospitalization. Method of measurement: Hospital anxiety and depression scale.;Physiologic factors. Timepoint: Every 2 hourse in day & before, Simultaneously and after of visiting. Method of measurement: Cardiac monitoring device.;Hospital anxiety. Timepoint: First day(before intervention in case groupe) and third dayof hospitalization( after intervention in controll groupe). Method of measurement: Hospital anxiety and depression scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRoza Ahmadian Yazdi

Baqiatallah University of Medical Sciences

ahmadianroza@yahoo.com+98 21 2228 9941

Outcome results

None listed

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