Caregiver Burden, Quality of Life, Family Function and Family Resilience Among Caregivers of Children With Medical Complexity.

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age20+
SponsorNational Taiwan University Hospital

About this trial

The purpose of this study is to employ a mixed methods research approach combining quantitative and qualitative methods to thoroughly understand the relationships among caregiver burden, quality of life, family functioning, and family resilience of children with medical complexity (CMC). The study aims to explore the individual and social factors influencing these variables and investigate the factors impacting caregiver burden, quality of life, family functioning, and family resilience of CMC caregivers. Finally, an integrative analytical framework will be proposed. The study seeks to provide guidance and recommendations for social support for caregivers of children with medical complexity in caregiving practices, aiming to promote the development of relevant policies and services.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Must be the primary caregiver of a child with medical complexity, providing care for at least 12 months.

Aged 20 years or older.

Must be a cohabiting family member of the child and have a biological relationship with the child.

Willing to participate in the study.

Disqualifiers

Diagnosed with a mental illness by a physician.

Assessed by the researcher as lacking the reading and comprehension abilities necessary to complete the study.

Trial population

The study population comprises primary caregivers of children with medical complexity (CMC)

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

  • non-intervention

    Other intervention

    non-intervention

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Caregiver Burden Inventory (CBI)

Scale: 0 to 96, with higher scores indicating greater caregiver burden. Description: This measure will assess the time dependence, developmental, physical, social, and emotional burdens experienced by caregivers of children with medical complexity.

Time frame
Less than 1 hour.
2

Quality of Life [Short Form Health Survey (SF-12)]

Scale: 0 to 100 for each domain, with higher scores indicating better quality of life. Description: This measure will evaluate the physical functioning, role physical, bodily pain, general health, vitality, social functioning, role emotional, and mental health of caregivers.

Time frame
Less than 1 hour.
3

Family Function (Family APGAR)

Scale: 0 to 10, with higher scores indicating better family function. Description: This measure will assess family adaptability, partnership, growth, affection, and resolve.

Time frame
Less than 1 hour.
4

Family Resilience Scale

Scale: 31 to 155, with higher scores indicating greater family resilience. Description: This measure will evaluate the belief systems, organizational patterns, and communication processes of families dealing with children with medical complexity.

Time frame
Less than 1 hour.

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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