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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06159127
Other study ID # SMART@Home
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 1, 2024
Est. completion date January 1, 2025

Study information

Verified date March 2024
Source Children's Hospital Medical Center, Cincinnati
Contact Kevin Hommel, PhD
Phone 513-803-0407
Email kevin.hommel@cchmc.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The proposed research addresses the limitations or lack of a digital platform to provide remote care of medically complex patients. Previous attempts have had poor clinical validity and suffered lack of patient engagement. The study team will deconstruct the previously implemented SMART platforms to create a roadmap, platform, and template to guide clinicians to create new tools. Results from Phase 1 of this project highlighted the need for connectivity between the SMART@Home app and Bluetooth-enable devices to provide objective disease activity data as well as integration with Epic electronic health record so that providers can use the data to inform treatment planning and decision making. A subsequent pilot user validation trial is also needed to confirm development goals were met. Conducting a pilot user validation trial of the SMART@Home asthma tracker, spirometer, and action plan is the purpose of the next phases of this study.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 25
Est. completion date January 1, 2025
Est. primary completion date December 30, 2024
Accepts healthy volunteers No
Gender All
Age group 11 Years to 17 Years
Eligibility Inclusion Criteria: - Patients diagnosed with a chronic medical condition requiring regular treatment, i.e., asthma - Ages 11-17 - English fluency for patient and caregiver Exclusion Criteria: - Diagnosis of pervasive developmental disorder in patient or caregiver as determined by medical chart review - Diagnosis of serious mental illness (e.g., schizophrenia) in patient or caregiver as determined by medical chart review

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
SMART@Home
Daily medication and diary completion reminders are provided to participants. Additional educational content regarding self-management skills will be provided.

Locations

Country Name City State
United States Cincinnati Children's Hospital Medical Center Cincinnati Ohio

Sponsors (1)

Lead Sponsor Collaborator
Children's Hospital Medical Center, Cincinnati

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of days app used Number of diaries completed by participant 3 months
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