Smart Technology Facilitated Patient-centered Venous Thromboembolism Management
- Sponsor
- Navy General Hospital, Beijing
- Study ID
- NCT06350331
- Status
- Enrolling By Invitation
Conditions
- Digital Health
- Health Education
- Venous Thromboembolism
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- mobile venous thromboembolism application (mVTEA) — OTHERmVTEA will assist in the management of patients during the post-hospitalization follow-up phase. The mVTEA's doctor terminal automatically sends VTE-related health education materials in different frequencies and contents based on the patient's knowledge of VTE prevention and treatment, as well as their risk of thrombosis and bleeding during follow-up. In addition, thrombosis physicians on the mVTEA's doctor terminal can deliver health education to patients based on their condition. This can be done through the mVTEA doctor-patient communication module, which includes text, photo, and voice interactions.
Study Details
Smart technologies, such as wearable devices, mobile technologies, and artificial intelligence, are being investigated for use in health management. These technologies have the potential to be applied in disease pre-warning, decision-making support, health education, and healthcare maintenance. They are expected to address the challenges in managing thrombosis, improve access to high-quality medical resources in various regions, and enhance the development of a network for thrombosis rescue and treatment prevention. The objective of this study is to evaluate the impact of mobile venous thromboembolism application (mVTEA) based patient-centered management of venous thromboembolism (VTE) on patients' perceptions of thromboprophylaxis, in order to enhance clinical practice and establish a foundation of evidence for managing patients with VTE.
Key Dates
- First listed
- Apr 5, 2024
- Start date
- Aug 17, 2024
- Status verified
- May 2025
- Primary completion
- Sep 30, 2025
- Completion
- Nov 30, 2025
Study Design
- Enrollment
- 256 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- PREVENTION
Arms
- Experimental: mVTEA Management GroupPatients randomly assigned to the mVTEA management group will be discharged with mVTEA-assisted patient-centered VTE management.
- No Intervention: Routine Management GroupPatients randomly assigned to the routine management group will be given routine post-discharge management in accordance with local clinical practice.
Primary Outcome Measure
VTE-KAP questionnaire score [ Time Frame: The third month after discharge from the hospital ]
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