the effect of controlled visits on the level of vital signs, SPO2 and satisfaction of care in Patient Care

the effect of controlled visits on the level of vital signs, SPO2 and satisfaction of care in cardiac patients admitted to the CCU

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20120414009469N3

Enrollment

124

Registered

2019-08-13

Start date

2019-08-23

Completion date

Unknown

Last updated

2019-10-07

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

Conditions

Vital signs, SPO2, satisfaction.

Interventions

Intervention 1: Intervention group: Controlled visit is applied twice a day and each time for 60 minutes for 3 days. Intervention 2: Control group: In controll groupe dont interfere & patient receiv

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:The patient has no prohibition to visit contentment of patient and relatives to participate in research Visitors are relatives of the first degree and are selected by the patient The age of the patients is between 18 and 60 years

Exclusion criteria

Exclusion criteria: Discharged from the ward before the third day of admission

Design outcomes

Primary

Measure	Time frame
Blood pressure. Timepoint: 5 minutes before intervention,30 minutes after beginning of intervention, 30 minutes after the end of the intervention. Method of measurement: sphygmomanometer.;Heart rate. Timepoint: 5 minutes before intervention,30 minutes after beginning of intervention, 30 minutes after the end of the intervention. Method of measurement: monitor.;Breathing. Timepoint: 5 minutes before intervention,30 minutes after beginning of intervention, 30 minutes after the end of the intervention. Method of measurement: monitor.;Spo2. Timepoint: 5 minutes before intervention,30 minutes after beginning of intervention, 30 minutes after the end of the intervention. Method of measurement: monitor.	—

Measure

Time frame

Blood pressure. Timepoint: 5 minutes before intervention,30 minutes after beginning of intervention, 30 minutes after the end of the intervention. Method of measurement: sphygmomanometer.;Heart rate. Timepoint: 5 minutes before intervention,30 minutes after beginning of intervention, 30 minutes after the end of the intervention. Method of measurement: monitor.;Breathing. Timepoint: 5 minutes before intervention,30 minutes after beginning of intervention, 30 minutes after the end of the intervention. Method of measurement: monitor.;Spo2. Timepoint: 5 minutes before intervention,30 minutes after beginning of intervention, 30 minutes after the end of the intervention. Method of measurement: monitor.

—

Secondary

Measure	Time frame
Satisfaction. Timepoint: After the intervention. Method of measurement: Satisfaction questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Adineh

Ahvaz University of Medical Sciences

mohadineh@gmail.com+98 61 3554 2036

Outcome results

None listed

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