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Research on the development of proactive health-oriented precise program for symptom management in patients after coronary artery stent implantation

Research on the development of proactive health-oriented precise program for symptom management in patients after coronary artery stent implantation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076596
Enrollment
Unknown
Registered
2023-10-12
Start date
2023-10-12
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Coronary Heart Disease

Interventions

Intervnention group:A knowledgebase-based poststenting management protocol
Conrtol group:Routine poststenting nursing methods

Sponsors

School of Nursing, University of South China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1.Longitudinal study Inclusion criteria: (1) Patients admitted to hospital with diagnosed coronary heart disease and successfully underwnt coronary artery stent implantation for the first time; (2) The place of residence is a community within the urban area of Hengyang City; (3) No comprehension and reading disabilities; (4) Volunteer to join this study. 2.Inclusion criteria for qualitative research focus group interviews with medical personnel: (1) Experience in diagnosis, treatment, and care of patients after coronary artery stenting or coronary heart disease; (2) Volunteer to participate in this study. Inclusion criteria for focus group interviews on the patient side: (1) Patients or their family members are successfully admitted to hospital for coronary artery disease and undergo coronary artery stenting; (2) The place of residence is a community within the urban area of Hengyang City; (3) Volunteer to participate in this study. 3.Inclusion criteria for feasibility analysis: (1) Patients admitted to hospital with diagnosed coronary heart disease and successfully undergo coronary artery stent implantation on the first day after admission; (2) The place of residence is a community within the urban area of Hengyang City; (3) No comprehension and reading disabilities; (4) Volunteer to join this study.

Exclusion criteria

Exclusion criteria: 1.Longitudinal study Exclusion criteria: (1) Patients with other serious diseases, malignant tumors, terminal stage, and dialysis; (2) Intermittent mental disorders. 2.Exclusion criteria for focus group interviews of medical personnel in qualitative research: (1) Cannot participate in focus group interviews within the specified time; (2) Cannot communicate in Mandarin or other languages; (3) Medical and nursing personnel who are interns or refreshers. Exclusion criteria for focus group interviews on the patient side: (1) Cannot participate in focus group interviews within the specified time; (2) Unable to communicate in Mandarin or other languages. 3.Exclusion criteria for feasibility analysis: (1) Patients with other serious diseases, malignant tumors, end-stage, and dialysis; (2) Intermittent mental disorders.

Design outcomes

Primary

MeasureTime frame
PROMIS Profile-57;

Secondary

MeasureTime frame
Health literacy level;The readmission rate caused by major cardiovascular adverse events;

Countries

China

Contacts

Public ContactQi Wang

School of Nursing, University of South China, Hengyang, Hunan

wangqi19992021@163.com+86 132 1801 3773

Outcome results

None listed

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