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Development and application of psychological empowerment intervention platform for ICU patients and their families based on wechat applet

Development and application of psychological empowerment intervention platform for ICU patients and their families based on wechat applet

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059945
Enrollment
Unknown
Registered
2022-05-14
Start date
2022-05-31
Completion date
Unknown
Last updated
2024-04-08

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

Conditions

critical illness

Interventions

1:WeChat applet-based psychological empowerment intervention

Sponsors

Fujian Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patient inclusion criteria: (1) Age = 18 years old; (2) Hemodynamic stability (mean arterial pressure>65mmHg); (3) Be able to communicate in Mandarin and obtain their informed consent. Inclusion criteria for family members: (1) Age =18 years, (2) Relatives who are recognized by the patient as primarily responsible for his or her daily living and assistance with medical tasks, (3) Knowing the diagnosis, condition, and treatment of the patient's disease, (4) Normal verbal and comprehension skills, and (5) Ability to use a smartphone, tablet or computer device, (6) Voluntary participation in this study.

Exclusion criteria

Exclusion criteria: Patient exclusion criteria: (1) Previous cardiac arrest; (2) Patients with unstable fracture, acute myocardial infarction, rupture of thoracic aortic aneurysm, myasthenia gravis, deep vein thrombosis, and other contraindications for getting out of bed; (3) Pregnancy; (4) Being involved in the research of other projects. Family exclusion criteria are: (1) Pre-existing or current mental illness; (2) People with varying degrees of cognitive impairment or a history of mental illness, and (3) Being involved in similar psychological intervention studies.

Design outcomes

Primary

MeasureTime frame
anxiety;

Secondary

MeasureTime frame
Depress;PTSD;self-efficacy;caregiver burden;Caregiver capacity;Fatigue ;Sense of disease uncertainty;Social Support;Quality of life;

Countries

China

Contacts

Public ContactLihong

Fujian Provincial Hospital

leehong99@126.com+86 137 0507 0219

Outcome results

None listed

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