Validity and reliability validation of the "Intensive Care Unit Version for Quality of Dying and Death for Family members in Japanese".

UMIN ID: UMIN000053822

Registered date:15/03/2024

Basic Information

• Recruitment status: Pending
• Health condition(s) or Problem(s) studied: Family members of patient who died in ICU
• Date of first enrollment: 2024/04/01
• Target sample size: 46
• Countries of recruitment: Japan
• Study type: Observational

Outcome(s)

• Primary Outcome: Retrospective survey for bereaved family members (within 6 months to 5 years after bereavement): Scores of ICU-QODD Japanese version Prospective survey for bereaved family members: Scores of ICU-QODD Japanese version Prospective survey for nurses: Scores of ICU-QODD Japanese version (for nurses)
• Secondary Outcome: Prospective survey for bereaved family members: Scores of FS-ICU Japanese version

Key inclusion & exclusion criteria

• Age minimum: 18years-old
• Age maximum: Not applicable
• Gender: Male and Female
• Exclude criteria: Retrospective survey for bereaved family members a. Consent cannot be obtained; b. Family members of patient who has been in the ICU or HCU for less than 48 hours; c. Family members who have not visited the patient during his/her stay in the ICU; d. Medical record data indicate a high psychological burden due to participation in the study; e. Have a mental illness; f. Non-native Japanese speaker Prospective survey for bereaved family members a. Consent cannot be obtained; b. Family members of patient who has been in the ICU or HCU for less than 48 hours; c. Family members who have not visited the patient during his/her stay in the ICU; d. Medical record data indicate a high psychological burden due to participation in the study; e. Have a mental illness; f. Non-native Japanese speaker; g. The researcher determined at the time of the survey request that the subject was inappropriate for the survey Prospective survey for nurses a. Consent cannot be obtained; b. Not in charge of a patient who has died in the ICU or HCU since the start of the study; c. Team member of this study

Related Information

• Primary Sponsor: Tokyo Healthcare University
• Source(s) of Monetary Support: N/A