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The impact of problem prompt list intervention on the care burden of family caregivers of patients with neurocritical subintensity: A quasi-experimental study

The impact of problem prompt list intervention on the care burden of family caregivers of patients with neurocritical subintensity: A quasi-experimental study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108807
Enrollment
Unknown
Registered
2025-09-05
Start date
2025-09-05
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

The patient's diagnosis falls under the category of neurocritical illness (including but not limited to cerebrovascular diseases, brain trauma, spinal cord injuries, etc., all neurological disorders). Although the condition has stabilized, there are still potential risks such as impaired consciousness, respiratory dysfunction, unstable circulation, etc., and continuous monitoring of vital signs, n

Interventions

Intervention Group:List of problem prompts + routine care
control group:routine care

Sponsors

The First Affiliated Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Patient: 1. Neurological sub-severe diseases (including but not limited to cerebrovascular diseases, head injury, spinal cord injury and other neurological diseases), although the condition has stabilized, there are potential risks, such as impaired consciousness, respiratory insufficiency, circulatory instability, etc., and key indicators such as vital signs, neurological function, intracranial pressure, and cerebral blood flow need to be continuously monitored. 2. The hospitalization time in the neurological sub-intensive care unit is expected to be 5 days or more; Caregivers: 1. Relatives of patients who undertake the main care tasks and participate in medical decision-making, and do not receive care remuneration; 2. Age>=18 years old, daily care time >=4 hours; 3. Have good listening and reading skills, no communication barriers; 4. Informed consent and able to participate in this study independently; 5. Only 1 primary caregiver.

Exclusion criteria

Exclusion criteria: Patients: Transferred to the area or transferred to a department or hospital at any stage after entering this study; Caregivers: 1. Suffering from diseases that affect cognitive function, such as Alzheimer's disease, stroke, etc.; 2. Suffering from severe mental disorders, such as schizophrenia, depression, etc.; 3. There are conditions such as language, vision and hearing impairment that affect the implementation of the study.

Design outcomes

Primary

MeasureTime frame
Caring burden;

Secondary

MeasureTime frame
Chinese version of the Auditory Learning Test Scale;Hospital Anxiety Scale;Multifactorial Memory Questionnaire;Adaptation Response Scale;

Countries

China

Contacts

Public ContactTan BinBin

The First Affiliated Hospital of Army Medical University

tanbinbin@tmmu.edu.cn+86 23 68765912

Outcome results

None listed

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