The Improve Acute Reperfusion Treatment Quality for Ischemic Stroke Through Spatiotemporal Computing in China

Acute Ischemic Stroke Clinical Trial

— IMPROVE-II  

Official title:

The Improve Acute Reperfusion Treatment Quality for Ischemic Stroke Through Spatiotemporal Computing in China (IMPROVE-II ) -A Multicenter, Evaluator-Blind, Cluster-Randomized Controlled Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06330051
• Other study ID #: KY 2023-184-02
• Status: Not yet recruiting
• Phase: N/A
• Start date: March 18, 2024
• Est. completion date: April 20, 2025

Study information

• Verified date: March 2024
• Source: Beijing Tiantan Hospital
• Contact: Zixiao Li, MD
• Phone: 00861067013383
• Email: lizixiao2008[@]hotmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study intends to construct the goal-oriented integrated intervention model for AIS in-hospital procedure through the spatiotemporal positioning and the P-D-C-A cycle for continuous improvement (FAST model). Then a multicenter, evaluator-blind, cluster-randomized controlled study aims to verify the validity and safety of this FAST model.

Description:

This study intends to construct the goal-oriented integrated intervention model, namely the preset first aid of acute ischemic stroke (AIS) process is the key time node in the target, through the intelligent bracelet automatic positioning, feedback system with real-time data as the carrier, through the P (Plan)-D (Do)-C (Check)-A (Act) cycle for continuous improvement, so as to shorten the delay time of reperfusion therapy and improve the rate of intravenous thrombolysis in AIS patients. Then a multicenter, evaluator-blind, cluster-randomized controlled study aims to verify the validity and safety of this FAST model. This study will recruit 20 secondary or tertiary hospitals that meet the inclusion criteria, mainly distributed in the Beijing-Tianjin-Hebei-Shanxi-Neimenggu region. After 2 months of baseline information collection, 10 hospitals will be selected and then randomly assigned to the control and intervention groups. Then, the intervention groups will install intelligent bracelet automatic positioning device and data feedback system based on spatiotemporal computing for 2 months. We will conduct training to ensure that only trained caregivers and researchers master the use of the application to maintain the integrity of the intervention, and all participants in the study will maintain the conventional procedure during this period. The FAST model intervention based on spatiotemporal computing technology should be uniformly started after installation and training in each intervention group hospital. As the knowledge gained from the training may affect the identification of AIS patients, the duration of the training will keep as short as possible, and the data collected during the time period receiving the training is not used for final analysis, in an effort to reduce possible contamination of the data. The intervention group will receive continuous intervention with a goal-oriented integrated intervention model based the spatiotemporal computing technology for 6 months and collect information, mainly the critical time information of the AIS reperfusion therapy process. In the control group, only information will be collected. We will compare the critical treatment time information, Door to Needle time and Door to Puncture time, etc., between the two groups and conduct a 3-month follow-up.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 600
• Est. completion date: April 20, 2025
• Est. primary completion date: March 18, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

Hospitals#

1. Secondary or tertiary public hospitals with an emergency department that receive patients with AIS.

2. Admit at least 50 patients of AIS within 4.5 hours after onset each month.

3. Have the capacity of intravenous thrombolytic therapy or/and endovascular treatment.

4. Voluntarily participate in this research and cooperate with the installation of bluetooth positioning device and the improvement of AIS emergency procedures.

5. Have good cooperation relationship among the department of Neurology, Emergency, Interventional department, Neurosurgery department, Laboratory department and Radiology department.

6. Have ability to establish or participate in the establishment of patient information database and arrange a person responsible for the collection of case information. Patients# Patients who are =18 years old are eligible for inclusion if they present with AIS diagnosed by CT and/or MRI, arrive at hospital within 4.5 hours after symptom onset, sign the informed consent form and agree to follow up until 3 months after stroke onset. Exclusion Criteria: Hospitals#

1. Hospital that unable to cooperate and complete the research.

2. Hospitals that are participating in other AIS medical quality improvement projects or related clinical trials. Patients#

1. Patients refuse to sign informed consent and follow up until 3 months after stroke onset.

2. Patients with mild nondisabling stroke symptoms (Defined as NIHSS=3, as any of the following: isolated facial paralysis; mild cortical blindness; mild hemianesthesia; mild hemiataxia.)

3. Life expectancy three-months or less by judgment of the investigator.

4. Participation in any interventional study that may affect the outcome

Related Conditions & MeSH terms

• Acute Ischemic Stroke
• Cerebral Infarction
• Ischemia
• Ischemic Stroke
• Stroke

Intervention

Behavioral:
• improvement acute reperfusion treatment quality for stroke through spatiotemporal computing
Intelligent bracelet automatic positioning device and data feedback system based on spatiotemporal computing technology Continuous in-hospital procedure improvement based on P-D-C-A cycle for AIS

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Beijing Tiantan Hospital

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The Door to Needle time (DNT) for intravenous thrombolytic therapy in eligible patients within 4.5 hours of onset.		Participants will be followed for the duration of hospital stay, an expected average of 2 weeks.
Secondary	The Door to Puncture time (DPT) for endovascular treatment within 6 hours of onset in eligible patients admitted to hospital within 4.5 hours of onset.		Participants will be followed for the duration of hospital stay, an expected average of 2 weeks.
Secondary	The rate of intravenous thrombolytic therapy in eligible patients within 4.5 hours of onset.		Participants will be followed for the duration of hospital stay, an expected average of 2 weeks.
Secondary	The rate of endovascular treatment within 6 hours of onset in eligible patients admitted to hospital within 4.5 hours of onset.		Participants will be followed for the duration of hospital stay, an expected average of 2 weeks.
Secondary	Incidence of symptomatic intracranial hemorrhage (sICH) within 36 hours of receiving reperfusion therapy.		Participants will be followed for the duration of hospital stay, an expected average of 2 weeks.
Secondary	Proportion of patients with 90-day favorable functional outcome.	mRS 0-1	Participants will be followed for 3 month after stroke onset.
Secondary	Proportion of patients with 90-day independent functional outcome.	mRS 0-2	Participants will be followed for 3 month after stroke onset.
Secondary	in-hospital mortality		Participants will be followed for the duration of hospital stay, an expected average of 2 weeks.
Secondary	90-day mortality		Participants will be followed for 3 month after stroke onset.