Family and Patient Outcomes After Pediatric Intensive Care (FOREVER) (FOREVER)

December 17, 2025 updated by: D'Or Institute for Research and Education

Family and Patient Outcomes After Pediatric Intensive Care

This study aims to evaluate in the Brazilian context, the impact of the implementation of a diary program on patient and family-centered outcomes after PICU discharge. The intervention investigated will be the use of hospital diaries for the critically ill child in a cross-over study, randomized by clusters in four PICUs of Rio de Janeiro. Family members of children aged 29 days to 12 years, admitted for more than 36 hours will be included and data collection will take place upon admission, at PICU discharge and 60 days after discharge from the PICU.

Family-centered outcomes assessed will be: satisfaction with care, anxiety and depression at discharge, incidence of anxiety, depression, PTSD, burden and quality of life in follow-up. Patient-centered outcomes will be assessed in children at discharge and follow-up - quality of life and incidence of new morbidities will be evaluated. The association of clinical, social and demographic variables with family- and patient-centered outcomes will be investigated on an exploratory basis. Burnout Syndrome in PICU health professionals will be assessed before and after the intervention as a proxy of intervention security for PICU staff.

Study Overview

Detailed Description

More than one third of parents and patients admitted to Pediatric Intensive Care Units (PICU) develop Anxiety, Depression and Posttraumatic Stress Disorder (PTSD), with consequent decrease in quality of life and great social impact, known as Pediatric and Family Post-Intensive Care Syndrome (PICS and PICS-F). Strategies that minimize negative outcomes after discharge have been adopted, such as the use of hospital diaries to regularly record the impressions of family members and health professionals about the patient's evolution, hosting parents and encouraging their direct participation in care.

This study aims to evaluate in the Brazilian context, the impact of the implementation of a diary program on patient and family-centered outcomes after discharge. The intervention investigated will be the use of hospital diaries for the critically ill child in a cross-over study, randomized by clusters in four PICUs of Rio de Janeiro, totaling 200 family members in the intervention group and 200 controls. Family members of children aged 29 days to 12 years, admitted for more than 36 hours will be included and data collection will take place upon admission, at discharge and 60 days after discharge from the PICU. Family-centered outcomes assessed will be: satisfaction with care, anxiety and depression at discharge, incidence of anxiety, depression, PTSD, burden and quality of life in follow-up. Quality of life and incidence of new morbidities will be evaluated in children at discharge and follow-up, as well as Burnout Syndrome in the health team. The association of clinical, social and demographic variables with family- and patient-centered outcomes will be investigated on an exploratory basis.

With this study, we aim to contribute to a better knowledge about different family-centered outcomes in intensive care, allowing reduction of health problems and the development of policies that seek to alleviate suffering, to humanize intensive environments and encourage participation of family members in child care during hospitalization.

Study Type

Interventional

Enrollment (Actual)

431

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Rio de Janeiro
      • Rio de Janeiro, Rio de Janeiro, Brazil, 22281-100
        • D'OR Institute for Research and Education

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

4 weeks to 12 years (Child)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Patients between age limits admitted in PICU for clinical or surgical reasons with 36 or more hours of stay and their main family member.
  • Physicians, registered nurses, nurse technicians, physical therapists and other professionals working in participants PICU involved in caring for patients and their families and taking notes in the diaries

Exclusion Criteria:

  • Patients admitted for monitorization or elective low-complexity surgeries
  • Patients readmitted between the first admission and the first follow-up visit
  • Patients in palliative care
  • Families with linguistic or comprehension barriers
  • Families residencies situated outside Rio de Janeiro metropolitan region

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: PICU with diaries

The main family member of a critically ill child will receive a diary upon PICU admission.

Except for the diaries intervention, this group of patients will be submitted to usual PICU routine care.

Diaries will be used by family members, PICU staff or even the patient himself. They will take daily notes expressing feelings and thoughts and describing events that might help chronologically to better understand the course of disease and PICU stay. Photographs and other important PICU memories may also be used in the diary.
No Intervention: PICU without diaries
This group of critically ill patients and family members will not receive diaries, but will also be submitted to usual PICU routine care.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Incidence of anxiety symptoms in family member from critically ill child.
Time Frame: 45-60 days after PICU discharge
Proportion of main family member positive for anxiety symptoms as measured by HADS (Hospital Anxiety and Depression Scale from Zigmond and Snaith), a self-report standardized 14-item questionnaire covering an anxiety 7-question subscale and a depression 7-question subscale. Each subscale includes Likert-scaled questions ranging from 0 to 3. Presence of anxiety symptoms will be determined when 9 or more points on each subscale.
45-60 days after PICU discharge
Incidence of depression symptoms in family member from critically ill child.
Time Frame: 45-60 days after PICU discharge
Proportion of main family member positive for depression symptoms as measured by HADS (Hospital Anxiety and Depression Scale from Zigmond and Snaith), a self-report standardized 14-item questionnaire covering an anxiety 7-question subscale and a depression 7-question subscale. Each subscale includes Likert-scaled questions ranging from 0 to 3. Presence of depression symptoms will be determined when 9 or more points on each subscale.
45-60 days after PICU discharge
Incidence of PTSD (Posttraumatic Stress Disorder) in family member from critically ill child.
Time Frame: 45-60 days after PICU discharge
Proportion of main family member positive for PTSD as measured by PCL-5 (Posttraumatic Stress Disorder Checklist for DSM-V - Diagnostic and Statistical Manual of Mental Disorders - V from Weathers et al), a self-report standardized 20-item questionnaire covering four dimensions of symptoms: intrusions, avoidance, negative alterations in cognitions and mood and alterations in arousal and reactivity. Each subscale includes Likert-scaled questions ranging from 0 (not at all) to 4 (extremely). Presence of PTSD symptoms when 33 or more total points or positivity in each DSM-V dimension.
45-60 days after PICU discharge

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluate family satisfaction with PICU care as measured by EMpowerment of PArents in THe Intensive Care 30 (EMPATHIC-30) questionnaire.
Time Frame: Until 72 hours after the patient discharge from Pediatric Intensive Care Unit
Quantify family satisfaction with PICU care as measured by EMPATHIC-30 (Latour et al), a self-report standardized 30-item questionnaire covering 5 domains: information, care and treatment, organization, parent participation and professional attitude. Each subscale includes Likert-scaled questions ranging from 1 (certainly no) to 6 (certainly yes). Higher scores, higher family satisfaction with care.
Until 72 hours after the patient discharge from Pediatric Intensive Care Unit
Evaluate alterations in family quality of life as measured by Short Form 12 (SF-12) questionnaire
Time Frame: 45-60 days after PICU discharge
Quantify family quality of life as measured by SF-12 (Ware et al), a self-report standardized 12-item questionnaire covering a mental and a physical component, with Likert-scaled questions ranging variedly. Higher scores, better quality of life.
45-60 days after PICU discharge
Incidence of Anxiety and Depression in family members of a critically ill child using HADS instrument upon PICU discharge.
Time Frame: Until 72 hours after the patient discharge from Pediatric Intensive Care Unit
Proportion of main family member positive for anxiety and depression as measured by HADS (Zigmond and Snaith), a self-report standardized 14-item questionnaire covering an anxiety 7-question subscale and a depression 7-question subscale. Each subscale includes Likert-scaled questions ranging from 0 to 3. Presence of anxiety or depression symptoms when 9 or more points on each subscale.
Until 72 hours after the patient discharge from Pediatric Intensive Care Unit
Incidence of New Morbidity in critically ill children at PICU discharge.
Time Frame: Until 72 hours after the patient discharge from Pediatric Intensive Care Unit
Incidence of New Morbidities in critically ill children admitted to a PICU, measured using the Functional Status Scale (FSS) upon admission, at PICU discharge and 60 days after PICU discharge. A raise in 3-points in FSS total score will be described as "New Morbidity", as assigned by Pollack et al.
Until 72 hours after the patient discharge from Pediatric Intensive Care Unit
Incidence of New Morbidity in critically ill children after PICU discharge.
Time Frame: 45-60 days after PICU discharge
Incidence of New Morbidities in critically ill children admitted to a PICU, measured using the Functional Status Scale (FSS) upon admission, at PICU discharge and 60 days after PICU discharge. A raise in 3-points in FSS total score will be described as "New Morbidity", as assigned by Pollack et al.
45-60 days after PICU discharge
Evaluate alterations in critically ill children Quality of Life as measured by Pediatric Quality of Life Questionnaire (PedsQL).
Time Frame: 45-60 days after PICU discharge
Quantify critically ill children Quality of Life after PICU discharge as measured by Pediatric Quality of Life Questionnaire (PedsQL).
45-60 days after PICU discharge
Prevalence of Burden in the main family member after PICU discharge measured with Zarit Burden Scale.
Time Frame: 45-60 days after PICU discharge
Prevalence of Burden in the main family member of a critically ill child after PICU discharge measured with Zarit Burden Scale (ZBI). This scale consists of 22 items rated on a 5-point Likert scale that ranges from 0 (never) to 4 (nearly always) with the sum of scores ranging between 0-88. Higher scores indicate greater burden.
45-60 days after PICU discharge
Perceptions of health professionals regarding the use of PICU diaries
Time Frame: One-month after the intervention period, which ends after the inclusion of 50 patient's family-members.
Perceptions of health professionals regarding the use of PICU diaries using a semi-structured questionnaire specifically developed for this study
One-month after the intervention period, which ends after the inclusion of 50 patient's family-members.
Perceptions of parents and main family members of a critically ill child regarding the use of PICU diaries
Time Frame: 45-60 days after PICU discharge upon intervention period
Perceptions of parents and main family members of a critically ill child regarding the use of PICU diaries using a semi-structured questionnaire specifically developed for this study
45-60 days after PICU discharge upon intervention period
Evaluate alterations in the three dimensions of the Maslach Burnout Inventory - emotional exhaustion, depersonalization and personal accomplishment - in PICU health professional.
Time Frame: One month before the beginning of the intervention in the PICU and one-month after the end of intervention period, which ends after the inclusion of 50 patient's family-members.
Evaluate alterations in PICU staff Burnout Syndrome scores, measured in the three dimensions of the Maslach Burnout Inventory - emotional exhaustion, depersonalization and personal accomplishment, as a proxy of intervention security for health professionals.
One month before the beginning of the intervention in the PICU and one-month after the end of intervention period, which ends after the inclusion of 50 patient's family-members.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Fernanda Lima-Setta, D'OR Institute for Research and Education

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 20, 2019

Primary Completion (Actual)

December 16, 2021

Study Completion (Actual)

December 16, 2021

Study Registration Dates

First Submitted

June 22, 2021

First Submitted That Met QC Criteria

July 5, 2021

First Posted (Actual)

July 14, 2021

Study Record Updates

Last Update Posted (Actual)

December 24, 2025

Last Update Submitted That Met QC Criteria

December 17, 2025

Last Verified

December 1, 2025

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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