Skip to content

Construction and Validation of a Precision Management Program for the Oral-Gut Axis in Older Patients with Cardiovascular Diseases

Construction and Validation of a Precision Management Program for the Oral-Gut Axis in Older Patients with Cardiovascular Diseases

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100064
Enrollment
Unknown
Registered
2025-04-02
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Cardiovascular Diseases

Interventions

Control group:The control group adopted routine oral and gut management measures.
Oral Group:Interventions aimed at improving oral health are framed by the Multi-Level Support System (MTSS) theory and integrated with the Social Cognitive Theory (SCT) approach to the design of behav
Gut Group:Interventions aimed at improving gut health were framed by the Multi-Level Support System (MTSS) theory and integrated with the Social Cognitive Theory (SCT) approach to behaviour change int
Oral - Gut Group:The intervention, which aims to improve both oral and gut health, is framed by the Multi-Level Support System (MTSS) theory and integrates the social cognitive theory (SCT) approach t

Sponsors

Tianjin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Be at least 60 years old. 2. Patients diagnosed with cardiovascular diseases (such as coronary heart disease, hypertension, arrhythmia, heart failure, heart valve disease, atherosclerosis, etc.) with stable conditions. 3. Participants who are permanent residents in Tianjin and can comply with regular follow - ups. 4. Have normal communication and reading comprehension abilities. 5. Be willing to participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Have taken antibiotics (such as Amoxicillin, etc.) within the past two weeks. 2. Suffering from severe systemic diseases or other diseases that may affect the effectiveness of the study intervention. 3. Suffering from severe mental illnesses and unable to cooperate with the study. 4. Currently participating in other clinical trials or research projects.

Design outcomes

Primary

MeasureTime frame
Oral health condition;Gastrointestinal symptom;Quality of life ;

Secondary

MeasureTime frame
Nutritional condition;Mental health condition;

Countries

China

Contacts

Public ContactXiaoying Zang

School of Nursing, Tianjin Medical University

xiaoyingzang@163.com+86 189 2069 7750

Outcome results

None listed

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