Incidence and Factors Associated to the Development of PICS-F Among ICU Relatives: A Longitudinal Exploratory Study

NCT05827354 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 175

Last updated 2024-04-09

No results posted yet for this study

Summary

The constellation of long-term psychological, physical, and cognitive impairments arising after a critical illness among family members of ICU survivors has been labeled as "Post Intensive Care Syndrome - Family" (PICS-F). Despite PICS-F awareness, the long-term issues faced by ICU family members remain poorly understood with several gaps in knowledge remaining such as the role of protective psychosocial factors, caregiver burden, or family satisfaction in the development of the syndrome.

This single-center, longitudinal exploratory study, aims to determine the incidence of each PICS-F impairment (psychological, physical, and cognitive) and to identify factors (during ICU stay and after hospital discharge) associated with the development or prevention of the PICS-F impairments among family members of ICU survivors of a public hospital in Chile.

Conditions

  • Post Intensive Care Syndrome
  • Family Members
  • Caregiver Burden
  • Critical Illness
  • Mental Health
  • Physical Health
  • Cognitive Impairment
  • Family Satisfaction
  • Resilience
  • Social Support

Sponsors & Collaborators

  • Agencia Nacional de Investigación y Desarrollo

    collaborator OTHER
  • Pontificia Universidad Catolica de Chile

    lead OTHER

Principal Investigators

  • Cristobal Padilla F., PhD · Pontificia Universidad Catolica de Chile

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-06-27
Primary Completion
2025-11-30
Completion
2025-11-30

Countries

  • Chile

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05827354 on ClinicalTrials.gov