Nurse-led integrated care for patients with multiple chronic conditions using telemonitoring

Nurse-led Integrated Care of Complex Patients Facilitated By Telemonitoring: The Safe, Managed, and Responsive Transitions (SMaRT) Study

Not applicable Interventional University Health Network, Toronto · NCT05543720

This study is testing if a nurse-led care program using a smartphone app can help patients with multiple chronic conditions stay healthier and avoid going back to the hospital after being discharged.

Quick facts

PhaseNot applicable
Study typeInterventional
Enrollment350 (estimated)
Ages18 Years and up
SexAll
SponsorUniversity Health Network, Toronto Academic / other
Locations4 sites (Brampton, Ontario and 3 other locations)
Trial IDNCT05543720 on ClinicalTrials.gov

What this trial studies

This study evaluates the effectiveness of nurse-led integrated care for patients with multiple chronic conditions through the use of a telemonitoring system called Medly. The trial will take place at four hospitals in Ontario, where patients recently discharged from the hospital will use a smartphone application to monitor their health metrics and symptoms. The app allows for personalized monitoring and provides self-care messages based on the patient's input. The goal is to improve care coordination and reduce the risk of readmission for these complex patients.

Who should consider this trial

Good fit: Ideal candidates are adults aged 18 and older who have been recently discharged from the hospital and have at least one complex chronic condition.

Not a fit: Patients who are not able to comply with the use of the telemonitoring application or have conditions that do not benefit from remote monitoring may not receive any benefit from this study.

Why it matters

Potential benefit: If successful, this approach could enhance the management of multiple chronic conditions and improve patient outcomes by providing timely interventions.

How similar studies have performed: Previous studies using telemonitoring for chronic conditions have shown promising results, indicating that this approach is supported by existing evidence.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. 18 years of age or older
2. Discharged from hospital or seen within 48 hours of discharge at Health Sciences North (HSN), William Osler Health Systems (WOHS), Women's College Hospital (WCH), and Markham Stouffville Hospital (MSH).
3. Have at least one complex chronic condition (i.e., heart failure, complex obstructive pulmonary disease (COPD), hypertension, diabetes, and/or depression) that would benefit if monitored through telemonitoring.
4. Able to comply with use of the telemonitoring application and applicable peripheral devices (e.g., able to stand on the weight scale, able to answer symptom questions, etc.)
5. Able to read, write and speak English or have a caregiver who is able to do so on their behalf.
6. Patients must have been discharged from hospital within 2 weeks during their recruitment into the study (or will be recruited prior to their discharge).

Exclusion Criteria:

1. Patients who are discharged from hospital with the intent to be admitted to a long-term care facility will be excluded.

Where this trial is running

Brampton, Ontario and 3 other locations

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Heart Failure,CongestiveMental HealthDiabetes MellitusChronic Obstructive Pulmonary DiseaseHypertensionTelemonitoringSmartphone applicationChronic disease management
Last reviewed 2026-06-09 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.