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Construction and Empirical Study of a Family Participatory Intelligent Management Support System for Chronic Heart Failure Comorbidity Patients

Construction and Empirical Study of a Family Participatory Intelligent Management Support System for Chronic Heart Failure Comorbidity Patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102896
Enrollment
Unknown
Registered
2025-05-21
Start date
2023-08-19
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Heart Failure

Interventions

Intervention group 1:The symptom management course of the digital "Dual Subject Symptom Precision Management of Chronic Heart Failure" platform combined with the Heart Failure Symptom Management Manua
Intervention group 2:The symptom management course of the digital "Dual Subject Symptom Precision Management of Chronic Heart Failure" platform
Control group:Routine post discharge management mode

Sponsors

Tianjin Fourth Center Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients: 1. Meeting the diagnostic criteria for heart failure patients in the 2018 Chinese Guidelines for the Diagnosis and Treatment of Heart Failure upon admission; 2. Cardiac failure as the primary admission diagnosis; 3. Age >= 18 years old; 4. Ability to read and express oneself in language, with no communication barriers. Caregiver: 1. Care time exceeding 6 hours per day; 2. Family members or close relatives of the patient; 3. Ability to read and express oneself in language, with no communication barriers; 4. Use smartphones during the research period.

Exclusion criteria

Exclusion criteria: Patients:1. Having experienced myocardial infarction, stroke, chronic obstructive pulmonary disease, renal failure, cancer, etc. in the past 3 months (combined with the above diseases, the symptoms of heart failure patients have a compound effect); 2. Intending to enter a care facility after discharge; 3. having participated in intervention trials other than routine care in the past three months. Caregivers: 1. Paid caregivers; 2. participated in intervention trials other than routine management in the past three months.

Design outcomes

Primary

MeasureTime frame
Symptom Status of Patients with Heart Failure and Caregivers;Psychological Status of Patients with Heart Failure and Caregivers;

Secondary

MeasureTime frame
Clinical outcomes;

Countries

China

Contacts

Public ContactXiaoying Zang

Tianjin Fourth Center Hospital

xiaoyingzang@163.com+86 189 2069 7750

Outcome results

None listed

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