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Construction and Empirical Research on Emotional Support Intervention Model for Elderly Patients with Cardiometabolic Diseases Multimorbid with Anxiety and/or Depression

Construction and Empirical Research on Emotional Support Intervention Model for Elderly Patients with Cardiometabolic Diseases Multimorbid with Anxiety and/or Depression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127653
Enrollment
Unknown
Registered
2026-07-03
Start date
2026-07-10
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Cardiometabolic Diseases Multimorbid with Anxiety and/or Depression

Interventions

Experimental Group:The experimental group received routine psychological care along with an emotion-support intervention based on a WeChat mini-program, lasting 12 weeks. Researchers were responsible
recommended 1–2 times per week
Control group:Provide routine psychological care to the subjects, including health education related to the disease, medication guidance, dietary and exercise advice
understand patients' psychological status through communication, establish a positive relationship, and offer comfort, encouragement, and emotional support for negative emotions such as anxiety and te

Sponsors

Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patient: 1. Age 60 years or older; 2. Diagnosed by a medical institution with at least one metabolic disorder—hypertension, diabetes, or dyslipidemia—and diagnosed with anxiety disorder, depressive disorder, or comorbid anxiety and depressive disorders according to the diagnostic criteria of either the "Clinical Practice Guidelines for Mental Disorders (2020 Edition)" or the "Clinical Descriptions and Diagnostic Criteria for Mental, Behavioral, and Neurodevelopmental Disorders" in the International Classification of Diseases, 11th Revision (ICD-11); 3. Blood pressure, fasting blood glucose, and lipid levels have been stable over the past four weeks, meaning no changes in treatment regimens (including medication type, dosage, and frequency), and no clinically significant fluctuations in monitoring indicators; no acute cardiovascular or cerebrovascular events or metabolic crises have occurred within the past four weeks; mental disorder is in a stable phase without acute episodes or marked symptom worsening; 4. Possesses basic skills in operating smartphones or tablets, capable of independently using mobile devices or with minimal assistance; 5. Fully informed about the study and voluntarily signs an informed consent form. Significant others: 1. Age 18 years or older; 2. Capable of clear verbal communication and able to provide informed consent; 3. A family member, neighbor, or friend designated by the elderly patient who engages in frequent emotional communication; 4. Possesses basic skills in operating smartphones or tablets, capable of independently using mobile devices.

Exclusion criteria

Exclusion criteria: For Patients: 1.Patients with impaired speech, hearing, or visual function, or with severe cognitive impairment that may affect their understanding of the study and cooperation. 2.Patients in the terminal stage of a disease with an estimated life expectancy of less than 6 months, who are unlikely to complete the full study participation. 3.Patients who have participated in other psychological intervention studies within the past 3 months, which may potentially affect the results of this study. 4.Patients who are unwilling to cooperate for other reasons. For significant others: 1.Individuals with serious mental disorders(schizophrenia) or cognitive impairments. 2.Individuals who are unwilling to cooperate for other reasons.

Design outcomes

Primary

MeasureTime frame
Positive and negative emotion;

Secondary

MeasureTime frame
Anxiety;Depression;Family Care Index;Quality of life;Blood pressure;Glycated hemoglobin;Total Cholesterol;Triglyceride;High-density lipoprotein;Low-density lipoprotein;

Countries

China

Contacts

Public ContactYuanyuan Jin

Soochow University

yyjin1109@suda.edu.cn+86 512 6512 5097

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026