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Investigating the effect of the presence of the patient's companion on patient anxiety and family satisfaction in patients admitted to the burn intensive care unit

Investigating the effect of the presence of the patient's companion on patient anxiety and family satisfaction in patients admitted to the burn intensive care unit

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240927063174N1
Enrollment
60
Registered
2024-11-16
Start date
2024-12-02
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Investigating the effect of the presence of the patient's companion on patient anxiety and family satisfaction in patients admitted to the burn critical care unit.

Interventions

Intervention 1: "Intervention group:"A family member will be present for six days and 90 minutes per day alternately (30 minutes at 10, 17, 22 o clock) during the patients waking hours. This family me

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: The age of patients should be 18-60 years Non-use of drugs related to nerves and anxiety and anxiety control in all participants of the study Being literate At least 24 hours have passed since the patient was admitted to the burn intensive care unit The patient should not be intubated and the level of consciousness of the patient should be =13 based on the Glasgow criteria The availability of a stable family member as a companion who can attend the study for six days The age of the accompanying patient should be between 18-60 years The family member's willingness to be at the patient's bedside for 6 days and every day for 90 minutes minouts alternately

Exclusion criteria

Exclusion criteria: Transfer, discharge or death of the patient before the sixth day of hospitalization Use of drugs or anti-anxiety and psychotropic drugs Not being present on two days or not being present at the patient's bedside for more than 12 hours Anxiety or excessive fatigue

Design outcomes

Primary

MeasureTime frame
Patient anxiety. Timepoint: The first day and the sixth day of the patient's hospitalization in the burn intensive care unit. Method of measurement: The visual anxiety scale will be used to check the patient's anxiety.

Secondary

MeasureTime frame
Family satisfaction. Timepoint: The first day and the sixth day of the patient's hospitalization in the burn intensive care unit. Method of measurement: The satisfaction measurement questionnaire (FS-ICU 24) will be used to measure the family's satisfaction.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSepideh Sepahi

Islamic Azad University

spydhspahy@gmail.com+98 45 3324 4778

Outcome results

None listed

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