Effect of Comprehensive Care Program on trauma patient comfort and satisfaction

the effect of implementation of the Comprehensive Care Program on trauma patient comfort and satisfaction in emergency department

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201402154443N8

Enrollment

104

Registered

2014-05-05

Start date

2014-02-19

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

trauma. Injuries to the head , Injuries to the neck, Injuries to the thorax ,Injuries to the abdomen, lower back, lumbarspine and pelvis , Injuries to the shoulder and upper arm, Injuries to the elbow and forearm , Injuries to the wrist and hand , Injuries t

Interventions

Intervention 1: control group will receive routine nursing care ( iv line, drug injection, ...). Intervention 2: Intervention group will receive , Comprehensive care program from the moment of arriv

Treatment - Other

control group will receive routine nursing care ( iv line, drug injection, ...).

Intervention group will receive , Comprehensive care program from the moment of arrival to the emergency, in addition to routine nursing care. The intervention consisted of a comprehensive care plan:

Eligibility

Sex/Gender

All

Age

18 Years to 78 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria :1- Patient admitted to hospital due to injuries for the first time 2- ability to read and write 3- comfort disturbing sickness absence 4- Patient awareness of time, place and person 5- The absence of mental illness 6-Ability to understand Persian conversation 7- Age over 18 years 8-Stay at least 4 hours in the emergency 9-Not taking psychotropic drugs 10-Being Muslim 11-Triage Level 3 Exclusion Criteria:1- The patient will need immediate surgery 2- Loss of consciousness 3-Discharge during the study with personal satisfaction 4-Lack of patient cooperation in data collection

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Comfort. Timepoint: Before and after intervention. Method of measurement: Eleven Likert scale score of comfort(0-10) Before intervention and Verbal Rating Scale comfort Kolcaba after intervention.	—

Secondary

Measure	Time frame
Satisfaction. Timepoint: after intervention. Method of measurement: Satisfaction Questionnaire modified form after intervention.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoumeh Zakerimoghadam

Tehran University of Medical Sciences

zakerimo@sina.tums.ac.ir+98 21 6692 7171

Outcome results

None listed

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