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Hospital-integrated Care Services

Exploring the Relationship Between Hospital-integrated Care Services and Caregiver Burden at a Medical Center in Northern Taiwan.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07201753
Enrollment
200
Registered
2025-10-01
Start date
2025-09-29
Completion date
2026-08-25
Last updated
2026-04-01

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

Conditions

Caregiver Burden of Caregivers, Hospital-Integrated Care Services

Brief summary

This study aims to explore the relationship between hospital-integrated care services and caregivers' psychological outcomes. The study will be conducted as a cross-sectional observational design at a medical center in northern Taiwan. Data will be collected from primary caregivers of hospitalized patients through validated questionnaires. The findings are expected to provide insights into improving caregiver support and enhancing patient and caregiver experiences during hospital stays.

Interventions

None listed

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Participants include inpatients receiving integrated inpatient care services at our hospital and their primary family caregivers. The patient or family member must have signed the consent form for integrated inpatient care services. The specific conditions are as follows: 1. Primary Caregiver Criteria: <!-- --> 1. The primary caregiver is a family member aged 18 years or older who can communicate in Mandarin or Taiwanese. 2. The family member is willing to sign the participant consent form. 2.Patient Criteria: <!-- --> 1. The patient has been admitted to the pilot ward for at least 24 hours.

Exclusion criteria

1. Patients who are discharged or transferred out of the pilot ward within 24 hours of admission. 2. If a patient is re-hospitalized during the study enrollment period and their primary caregiver is the same as in the previous enrollment, the subsequent duplicate case will be excluded. 3. Patients without family members will be enrolled in the ward's mandatory integrated inpatient care service program, but follow-up care issues will be handled by social workers.

Design outcomes

Primary

MeasureTime frameDescription
Total score of caregiver burden as measured by the Zarit Burden Interview (ZBI-22)Within 48 hours prior to hospital discharge.The Traditional Chinese version of the ZBI-22 includes 22 Likert-type items (0-4); total scores range from 0 to 88, with higher scores indicating greater burden.

Secondary

MeasureTime frameDescription
Total score of caregiver burden as measured by the Caregiver Burden Inventory (CBI)Within 48 hours prior to hospital discharge.The Traditional Chinese version of the CBI includes 24 Likert-type items (0-4); total scores range from 0 to 96, with higher scores indicating greater burden across multiple domains.
Subscale scores of anxiety and depression as measured by the Hospital Anxiety and Depression Scale (HADS)Within 48 hours prior to hospital discharge.The Traditional Chinese version of HADS contains 14 items, 7 for anxiety and 7 for depression. Each item is scored 0-3; subscale scores range from 0 to 21, with higher scores indicating more severe symptoms.
Domain mean scores of inpatient satisfaction as measured by the standardized hospital inpatient satisfaction surveyWithin 48 hours prior to hospital discharge.The hospital's standardized inpatient satisfaction survey includes 31 items. Each item is rated on a 5-point Likert-type scale, with response anchors varying by question (e.g., from "very sufficient" to "very insufficient," or from "strongly agree" to "strongly disagree"). Scores are calculated as domain means, with higher scores indicating greater inpatient satisfaction.

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 2, 2026