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Current Status and Influencing Factors Analysis of Post-ICU Syndrome and Quality of Life of Family Members of Adult Critical Patients Two Weeks After Discharge from ICU

Current Status and Influencing Factors Analysis of Post-ICU Syndrome and Quality of Life of Family Members of Adult Critical Patients Two Weeks After Discharge from ICU

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100968
Enrollment
Unknown
Registered
2025-04-17
Start date
2024-01-01
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

None

Interventions

Observation group:None

Sponsors

Affiliated Hospital of Zunyi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Stage 1 (Preparation): Qualitative interview (1) The length of stay in the ICU was >=48 hours; (2) The age of the patients and their families was >=18 years; (3) Be conscious, able to communicate, and willing to express their feelings; (4) Diagnosis of PICS-F. Stage 2 (Survey Analysis Phase): Cross-sectional Survey (1) The length of stay in the ICU was >=48 hours; (2) The age of the patients and their families was >=18 years; (2) key decision-makers and caregivers of ICU patients; (3) There were no cognitive and communication impairments at the time of investigation; (4) Informed consent and voluntary participation in this study.

Exclusion criteria

Exclusion criteria: Phase I (Preparation Phase): Qualitative Interviews (1)Limited by educational level or other factors, unable to answer relevant questions or fill in information. (2)Unwilling to participate in this study or withdraw midway. The second phase (Survey and Analysis Phase): Cross-sectional survey (1) Individuals with psychiatric disorders or other severe organic diseases; (2) Individuals with severe hearing or speech impairments that prevent communication; (3) Individuals who have experienced other severe traumatic stress events in the past three months.

Design outcomes

Primary

MeasureTime frame
Hospital Anxiety and Depression Scale;Impact of Event Scale-Revised;Pittsburgh Sleep Quality Index;Fatigue Assessment Instrument;Critical Care Family Needs Inventory;Control Preference Scale;Zarit Caregiver Burden Interview;Perceived social support scale;Activity of Daily Living Scale;Survey Form on General Information of Patients and Their Families;No intervention measures were implemented.;

Countries

China

Contacts

Public ContactYou Yuan

The Affiliated Hospital of Zunyi Medical University

yuanyou94@foxmail.com+86 187 9812 0470

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 7, 2026