The Impact of a Personalized Care Intervention on 90-day Post-Discharge Care

Not Applicable

Completed

• Conditions: Cardiovascular Diseases
• Interventions: Behavioral: Laguna Coach and App Intervention Group

• Registration Number: NCT06146582
• Lead Sponsor: Laguna Health, Inc

Brief Summary

The purpose of this 90 day study is to demonstrate the extent to which participants with cardiovascular conditions can improve their recovery at home through a mobile app, support and resources made available to them after hospitalization. The study will evaluate the effectiveness of personal care intervention support, including one-on-one guidance, educational information, check-ins, and Laguna's mobile app to help participants recover better after hospitalization.

Detailed Description

This study was designed to provide support to a select group of participants by supplementing the hospital-provided discharge instructions. Laguna integrated hospital provided clinical guidance and Laguna's personalized contextual care protocols, with the goal of improving health outcomes and reducing readmissions within 90 days post-discharge.

Particiants in the intervention group received support from Laguna Health via Laguna's mobile app, phone, video, text, or web chat. Laguna provided contextual support to remove recovery barriers to these intervention participants.

Study Timeline

• Study Start: 2021-11-15
• Primary Completion: 2023-10-05
• Study First Submitted: 2023-11-17
• Study First Submitted QC: 2023-11-17
• Study First Posted: 2023-11-24
• Study Completion: 2023-12-29
• Status Verified: 2024-03
• Last Update Submitted: 2024-03-18
• Last Update Posted: 2024-03-20

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 187

Inclusion Criteria

• Admitted to the hospital with a diagnosis of a cardiovascular disorder as defined by the coded diagnoses for that admission
• Discharged to home
• Converse in English
• Uses a telephone (landline or cell phone)

Exclusion Criteria

• Participant unable to provide informed consent
• Participant lacks cognitive ability to participate in the study interventions as judged by the individual initiating the consenting process

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Intervention Arm	Laguna Coach and App Intervention Group	Group received support from Laguna Coaches

Primary Outcome Measures

Name	Time	Method
Unplanned All Cause Readmission Rate	90 Days Post-Discharge

Trial Locations

Locations (1)

Mayo Clinic; 🇺🇸 Rochester, Minnesota, United States