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The development and effectiveness of a complex family adaptation intervention strategies among families of hospitalized child with cancer

The development and effectiveness of a complex family adaptation intervention strategies among families of hospitalized child with cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076764
Enrollment
Unknown
Registered
2023-10-18
Start date
2024-07-15
Completion date
Unknown
Last updated
2024-07-15

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

Conditions

Pediatric cancer

Interventions

intervention group:multi-component family-based interventions
control group:stress managementcourse and usual follow-up

Sponsors

Xiangya School of Nursing, Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. A family included one child with a tumor and one or more primary caregivers; 2. The child meets the following inclusion criteria: (1) Initial leukemia/cranial malignancy diagnosis on pathology and knowledge of the condition; (2) Aged 5-12 years; (3) No history of psychiatric illness; (4) The child agrees to participate in the study and his or her parents give written consent for the child to participate; 3. Inclusion of the children's caregivers: We will attempt to recruit multiple family members to participate in this project, including primary caregivers such as mothers and fathers. We will recruit other primary caregivers for children whose parents are not primary caregivers, such as grandparents or other relatives.

Exclusion criteria

Exclusion criteria: 1. Is participating or has previously participated in a psychosocial intervention pilot study; 2. Has a comorbid physical severe illness or has experienced a significant life event other than illness in the past six months (e.g., parental divorce, death of a parent, etc.); 3. Has an end-stage illness; 4. Has a cognitive, expressive, or severe visual impairment and other conditions that make inclusion inappropriate due to illness (e.g., parental history of mental illness) as assessed by relevant assessments; 5. Will be excluded if the child is absent from the intervention or proposes to withdraw due to a change in condition in the middle of the course or for other reasons.

Design outcomes

Primary

MeasureTime frame
Family Adaptability and Cohesion Environment Scale;Posttraumatic Stress Disorder-Reaction Index(Child);Impact of Event Scale Revised (caregiver);Positive and Negative Affect Scale (Child);The Depression Anxiety Stress Scale (caregiver);EuroQol five-dimension questionnaire (Child);EuroQol five-dimension questionnaire (caregiver);

Secondary

MeasureTime frame
Salivary Cortisol;Sleep;Family Inventory of Life Events and Changes (caregiver));Social Support Rating Scale (caregiver);Simplified Coping Style Questionnaire (caregiver);Child Posttraumatic Cognitions Inventory (Child);the Stress Appraisal Measure (caregiver);

Countries

China

Contacts

Public ContactGu Can

Xiangya School of Nursing, Central South University

gucan_cs@csu.edu.cn+86 138 7488 1548

Outcome results

None listed

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