AzTrials
AzTrials

Venous ThromboembolismSmaPENCT06382038

Smart Technology Facilitated Patient-centered Care for Patients With Pulmonary Thromboembolism

A study testing mobile venous thromboembolism application (mVTEA) in people with Venous Thromboembolism and Pulmonary Thromboembolisms, run by Navy General Hospital, Beijing at 1 site in China.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

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. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
mobile venous thromboembolism application (mVTEA)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
2,972 participants
Where
1 siteChina
Study dates
20 Aug 2026to 30 Sep 2029
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Inpatients aged ≥18 years;
  • PTE confirmed through imaging examinations, meeting at least one of the following criteria: a.Newly diagnosed PTE during the current hospitalization; b. Prior PTE with imaging evidence of residual thrombus.
  • Signed informed consent.

Who cannot join

  • Previous PTE combined with CTEPH;
  • Mental retardation or a combination of other serious illnesses that make them incapable of living on their own;
  • Inability to use smartphones, computer tablets and other smart devices;
  • Being pregnant or breastfeeding;
  • Have participated in similar trials or are undergoing other clinical trials.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

ZHI-GENG JIN, Doctor contact

8615801402223

lwgjzg@163.com

China1 site, 1 recruiting
  • Sixth Medical Center of Chinese PLA General Hospital

    Beijing, Beijing Municipality, 100048

    ZHI-GENG JIN, Doctor, 8615801402223, lwgjzg@163.com

    Recruiting

Other trials in China

About this study

Official title: Smart Technology Facilitated Patient-centered Care for Patients With Pulmonary Thromboembolism:A Multicenter, Randomized Controlled Trial

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.

This study aims to evaluate the effects of a smart technology-assisted, patient-centered mobile health application for pulmonary thromboembolism management (mPEA) on the long-term outcomes of patients with pulmonary thromboembolism (PTE). The findings are expected to inform clinical practice and provide an evidence base for the long-term management of patients with PTE.

Being tested
mobile venous thromboembolism application (mVTEA)
Keywords
Venous Thromboembolism, Pulmonary Thromboembolisms, Digital Health
Medical subject headings
Venous Thromboembolism, Pulmonary Embolism

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • mobile venous thromboembolism application (mVTEA)Other

    mVTEA will assist in the management of patients during the post-hospitalization follow-up phase. The mVTEA's doctor terminal automatically sends venous thromboembolism (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, voice, and video communication.

Study groups in NCT06382038
Study groupRoleWhat they receive
mPEA Management GroupExperimentalPatients randomly assigned to the mPEA management group will be discharged with mPEA-assisted patient-centered PTE management.
Receives: Other: mobile venous thromboembolism application (mVTEA)
Routine Management GroupNo interventionPatients randomly assigned to the routine management group will be given routine post-discharge management in accordance with local clinical practice.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. VTE-related composite event

    The primary outcome was the occurrence of VTE-related composite event at 1-year follow-up, which was defined as a composite of recurrent VTE, newly diagnosed deep vein thrombosis (DVT), chronic thromboembolic pulmonary hypertension (CTEPH), major bleeding, VTE-related rehospitalization, and all-cause death.

    Measured: At 1-year follow-up

Secondary outcomes (15)
  1. VTE events

    VTE events will be documented at the 3, 6, 12, and 24-month follow-up after discharge. VTE events are categorized into two groups: recurrent VTE and newly diagnosed DVT.

    Recurrent VTE is defined as the appearance of new evidence of VTE after acute VTE has been treated in the acute phase (2 weeks) with significant clinical improvement in signs and symptoms. According to the time of VTE recurrence, it is further categorized into early VTE recurrence (within 3 months after the last VTE occurrence) and late VTE recurrence (more than 3 months after the last VTE occurrence).

    DVT that occurred for the first time after discharge during the study period is classified as newly diagnosed DVT.

    Measured: At 3, 6, 12, and 24-month follow-up

  2. Chronic thromboembolic pulmonary hypertension (CTEPH)

    The diagnosis of CTEPH will be documented at the 3, 6, 12, and 24-month follow-up.

    Measured: At 3, 6, 12, and 24-month follow-up

  3. Chronic thromboembolic pulmonary disease (CTEPD)

    The diagnosis of CTEPD will be documented at the 3, 6, 12, and 24-month follow-up after discharge.

    Measured: At 3, 6, 12, and 24-month follow-up

  4. Post-pulmonary embolism syndrome (PPES)

    The diagnosis of PPES will be documented at the 3, 6, 12, and 24-month follow-up after discharge

    Measured: At 3, 6, 12, and 24-month follow-up

  5. Major bleeding

    The major bleeding events as defined by the International Society on Thrombosis and Hemostasis (ISTH) will be documented at the 3, 6, 12, and 24-month follow-up after discharge.

    Measured: At 3, 6, 12, and 24-month follow-up

  6. VTE-related hospitalization

    Rehospitalization due to VTE recurrence, progression, or complications related to VTE treatment will be documented during the follow-up.

    Measured: At 3, 6, 12, and 24-month follow-up

  7. Death

    Death will be documented during the follow-up. It is categorized into all-cause death and PTE-related death. All-cause death is defined as death that occurs during the study period, regardless of cause. PTE-related death is defined as death that is unequivocally due to PTE.

    Measured: At 3, 6, 12, and 24-month follow-up

  8. Patient-Reported Outcome Events (PROs)

    PROs will be documented during the 3, 6, 12, and 24-month follow-up after discharge.

    PROs refer to information directly conveyed by patients themselves concerning their health status, symptoms, functional capacity, or adverse events related to treatment, without the need for interpretation or mediation by clinicians or other third parties.

    Measured: At 3, 6, 12, and 24-month follow-up

  9. Generic quality of life

    Generic, non-disease-specific health-related quality of life (QoL) is assessed using the EuroQol 5-Dimension 5-Level (EQ-5D-5L) questionnaire and its corresponding visual analogue scale at 6, 12, and 24 months after discharge. Briefly, the EQ-5D-5L generates an overall index that ranges from 0 (lowest generic QoL) to 1 (highest generic QoL) and is calculated based on country-specific reference value sets. The EQ-5D-5L health index was calculated with the value set for China. The EuroQol visual analogue scale ranges from 0 to 100, with higher scores indicating better health.

    Measured: At 6, 12, and 24-month follow-up

  10. Costs of management for healthcare staff

    Costs of healthcare staff training (training duration × hourly wage), including training on standardized management of pulmonary embolism and the use of mVTEA; costs associated with post-discharge patient management by healthcare personnel (such as follow-up management, rehabilitation management, health counseling, and comorbidity management), calculated as (consultation time/re-hospitalization time × hourly wage); and development costs for mobile technology and intelligent algorithms.

    Measured: At 3, 6, and 12-month follow-up

  11. Treatment costs for VTE-related patients

    Treatment costs for VTE-related patients within 12 months post-discharge: These include registration fees, diagnostic costs, and treatment expenses incurred during visits to community clinics, hospital emergency departments, or specialist outpatient clinics due to changes in PTE condition (such as VTE recurrence, newly diagnosed DVT, bleeding, CTEPH, CTEPD, or PPES). They also encompass diagnostic and treatment expenses during hospital admissions in community or specialist settings due to changes in PTE condition. Additionally, costs arising from routine VTE follow-ups (without any changes in VTE-related conditions) at community clinics, hospital emergency departments, or specialist outpatient clinics are included.

    Measured: At 1-year follow-up

  12. Treatment costs for non-VTE-related patients

    Treatment costs for non-VTE-related patients within 12 months post-discharge: These comprise registration fees, diagnostic costs, and treatment expenses associated with visits to community clinics, hospital emergency departments, or specialist outpatient clinics for non-VTE-related conditions, as well as diagnostic and treatment expenses during hospital admissions in community or specialist settings for non-VTE-related diseases.

    Measured: At 3, 6, and 12-month follow-up

  13. Anticoagulant adherence

    Adherence would be assessed at months 3, 6, and 12 after discharge (defined as: the number of patients taking anticoagulants as prescribed/total number of patients at follow-up time point × 100%).

    Measured: At 3, 6, and 12-month follow-up

  14. Probability of PTE progression

    Clinical cure rate of PTE (defined as the numbers of patients without VTE recurrence, newly diagnosed DVT, bleeding, CTEPH, CTEPD, PPES, or all-cause mortality / total number of patients at the follow-up time point × 100% ); VTE (PTE/DVT) recurrence rate; incidence rate of newly diagnosed DVT; bleeding incidence rate; major bleeding incidence rate; non-major bleeding incidence rate; CTEPH incidence rate; CTEPD incidence rate; PPES incidence rate; all-cause mortality rate; PTE-related mortality rate would be collected.

    Measured: At 3, 6, and 12-month follow-up

  15. Effectiveness evaluation

    Quality-Adjusted Life Year(QALY) with EQ-5D-5L questionnaire would be investigated at 3, 6, and 12 months post-discharge and when the occurrence of VTE-related adverse events, including newly diagnosed DVT, bleeding, CTEPH, CTEPD, PPES, or all-cause mortality.

    Measured: At 3, 6, and 12-month follow-up

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Apr 2024
  2. Study start20 Aug 2026
  3. Primary completion30 Sep 2028 (estimated)
  4. Study completion30 Sep 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Model description
This study is a multicenter, prospective, randomized controlled trial with a superiority design. Consecutively recruited patients with PTE will be randomly assigned in a 2:1 ratio to either the interventive arm (mPEA management) or the routine management arm.
Masking
Triple blind
Who is masked
Care provider, Investigator, Outcomes assessor
Enrolment
2,972 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06382038
Sponsor's protocol ID
HZKY-PJ-2024-19
Acronym
SmaPE
Status last verified
Sep 2026
First submitted
18 Apr 2024
Last updated
9 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Valerio L, Mavromanoli AC, Barco S, Abele C, Becker D, Bruch L, Ewert R, Faehling M, Fistera D, Gerhardt F, Ghofrani HA, Grgic A, Grunig E, Halank M, Held M, Hobohm L, Hoeper MM, Klok FA, Lankeit M, Leuchte HH, Martin N, Mayer E, Meyer FJ, Neurohr C, Opitz C, Schmidt KH, Seyfarth HJ, Wachter R, Wilkens H, Wild PS, Konstantinides SV, Rosenkranz S; FOCUS Investigators. Chronic thromboembolic pulmonary hypertension and impairment after pulmonary embolism: the FOCUS study. Eur Heart J. 2022 Sep 21;43(36):3387-3398. doi: 10.1093/eurheartj/ehac206.

    PubMed 35484821
  • Schulman S, Angeras U, Bergqvist D, Eriksson B, Lassen MR, Fisher W; Subcommittee on Control of Anticoagulation of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Definition of major bleeding in clinical investigations of antihemostatic medicinal products in surgical patients. J Thromb Haemost. 2010 Jan;8(1):202-4. doi: 10.1111/j.1538-7836.2009.03678.x. Epub 2009 Oct 30.

    PubMed 19878532

Questions about this trial

What is this clinical trial studying?

A study testing mobile venous thromboembolism application (mVTEA) in people with Venous Thromboembolism and Pulmonary Thromboembolisms, run by Navy General Hospital, Beijing at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 9 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact ZHI-GENG JIN, Doctor (8615801402223, lwgjzg@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

VTE-related composite event (time frame: At 1-year follow-up). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06382038, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Sep 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in