Study on symptom trajectory of pediatric post-intensive care syndrome and the prevention intervention model of family stress inoculation training

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100045766

Enrollment

Unknown

Registered

2021-04-24

Start date

2021-04-23

Completion date

Unknown

Last updated

2021-12-06

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

Conditions

pediatric post-intensive care syndrome

Interventions

Experimental group:Family stress inoculation training

Control group:Routine care

Eligibility

Sex/Gender

All

Age

8 Years to 14 Years

Inclusion criteria

Inclusion criteria: Both the children and the parents meet the following inclusion criteria: Children: 1.8 years = 24 hours; 3.No history of mental illness or cognitive impairment; 4.Informed consent and voluntary participation. The children and his parents signed an informed consent form. Parents: 1.Parents of children admitted to PICU for treatment; 2.The main caregivers and medical decision-makers of the children; 3.Age >=18 years old; 4.Have communication skills and certain reading ability; 5.Informed consent and voluntary participation. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: Children and parents who meet any of the following items can be excluded. Children: 1.Resident observation after surgery; 2.No clear caregiver; 3.Mental retardation or mental retardation; 4.Participate in intervention studies that may change the follow-up outcome; 5.Estimated survival time <=48 hours; 6.Orphans. Parents: 1.Severe audiovisual impairment, which affects the understanding or answerer of the question; 2.Participate in intervention studies that may change the follow-up outcome.

Design outcomes

Primary

Measure	Time frame
Child Quality of life Assessment Scale;Child Behavior Cheek List;Self-Rated Anxiety Scale;Self-Rated Depression Scale;Standford Acute Stress Reaction Questionnaire;Screen for Child Anxiety Related Emotional Disorders;Depression Self-rating Scale for Children;Child Stress Disorders Checklist;Sleep disturbance scale for children;Impact of Event Scale-Revised;Family Impact Module Scale;Posttraumatic Growth Inventory;Revised Post-traumatic Growth Inventory for Children;Eye-tracking test;Event-related Potential;Functional near-infrared spectroscopy;	—

Measure

Time frame

Child Quality of life Assessment Scale;Child Behavior Cheek List;Self-Rated Anxiety Scale;Self-Rated Depression Scale;Standford Acute Stress Reaction Questionnaire;Screen for Child Anxiety Related Emotional Disorders;Depression Self-rating Scale for Children;Child Stress Disorders Checklist;Sleep disturbance scale for children;Impact of Event Scale-Revised;Family Impact Module Scale;Posttraumatic Growth Inventory;Revised Post-traumatic Growth Inventory for Children;Eye-tracking test;Event-related Potential;Functional near-infrared spectroscopy;

—

Secondary

Measure	Time frame
Family Functioning Scale;Pittsburgh sleep quality index;Social Support Rating Scale;Conners Parent Symptom Questionnaire;	—

Countries

China

Contacts

Public ContactHu Rongfang

Fujian Medical University

756672745@qq.com+86 13509366729

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026