A prospective cohort observational study to clarify the incidence of post-intensive care syndrome and the impact of information provision in families of patients with out-of-hospital cardiac arrest

A prospective cohort observational study to clarify the incidence of post-intensive care syndrome and the impact of information provision in families of patients with out-of-hospital cardiac arrest - A prospective cohort observational study to clarify the incidence of post-intensive care syndrome and the impact of information provision in families of patients with out-of-hospital cardiac arrest

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000040869

Enrollment

Registered

2020-08-13

Start date

2020-08-03

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

family&#39

Interventions

Non-intervention group: No pamphlet intervention Medical explanation group:Providing information through pamphlets that help families understand the patient&#39

s situation and accept the current situation Medical/social explanation group:In addition to the control group pamphlet, we will provide information by pamphlet containing information on social resour

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Family members over 20 years old of patients over 20 years old admitted for out-of-hospital cardiac arrestA family of patients who have been carried in a cardiac arrest due to cardiovascular disease or a cardiac arrest due to cerebrovascular diseaseFamily members who can obtain consent from their families to participate in the studyFamily who can answer questionnaire using Google form

Exclusion criteria

Exclusion criteria: If the patient died before obtaining the consent document When the disease caused by hospitalization is hospitalization due to re-hospitalization such as recurrence In addition, when the doctor in charge judges that the registration of this study is inappropriate

Design outcomes

Primary

Measure	Time frame
Impact of Event Scale-Revised:IES-R	—

Secondary

Measure	Time frame
Hospital Anxiety and Depression Scale:HADS EQ-5D-5L Brochure comprehension, family physical characteristics/social status/history of mental illness, patient physical characteristics/social status/treatment progress information	—

Countries

Japan

Contacts

Public ContactKeisuke Harada

Sapporo Medical University Hospital Emergency medicine

keisukeh@sapmed.ac.jp011-611-2111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026