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The effect of orientation tour on the anxiety of patients

The effect of orientation tour on the anxiety of patients candidate cardiac Electro-Physiology Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016072729102N1
Enrollment
80
Registered
2017-07-25
Start date
2017-05-22
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

Anxity. Other nonpsychotic mental disorders

Interventions

Intervention 1: In the intervention group, in addition to routine care, orientation tour during a meeting of 30 to 40 minutes to form groups of 3 to 5 members will be done. And the control group did n
Treatment - Drugs
In the intervention group, in addition to routine care, orientation tour during a meeting of 30 to 40 minutes to form groups of 3 to 5 members will be done. And the control group did not. The anxiety
Control group: In control group no intervention has been done without routine care.

Sponsors

Shahed University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: minimum age is 18 years and the maximum age is 80 years; The patient is done under study Cardiac Electrophysiology and Angiography for the first time; lack history of thyroid disease, mental disorder, anxiety, cardiac valve diseases and any cardiac invasive interventions such as Electro-Physiological Study and Trans Esophageal Echocardiography. Exclusion criteria: If any reason for the emergency cardiac interventions such as Electro-Physiological Study; Angiography, and or admitted in the CCU; Clinical illness conditions and unstable hemodynamic situation; Not wanting to continue working in research.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety level. Timepoint: Before intervention, after intervention, 3 hours after the end of heart Electro-Physiology Study. Method of measurement: State-Trait Anxiety Inventory (STAI).

Secondary

MeasureTime frame
Systolic Blood Pressure. Timepoint: Before intervention, after intervention, 3 hours after the end of heart Electro-Physiology Study. Method of measurement: Mercury Manometers.;Diastolic Blood Pressure. Timepoint: Before intervention, after intervention, 3 hours after the end of heart Electro-Physiology Study. Method of measurement: Mercury Manometers.;Mean Arterial Pressure. Timepoint: Before intervention, after intervention, 3 hours after the end of heart Electro-Physiology Study. Method of measurement: Mercury Manometers.;Heart Rate. Timepoint: Before intervention, after intervention, 3 hours after the end of heart Electro-Physiology Study. Method of measurement: Control pulse rate manually.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMajid Asgari

Shahed University

Majidasgari1352@gmail.com+98 21 2297 8457

Outcome results

None listed

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