Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
96 participants
INTERVENTIONAL
2027-08-01
2030-07-30
Brief Summary
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-Is an adaptive intervention (personalizing the intensity of support based on patients' needs) efficacious for promoting medication adherence Researchers will compare the adaptive intervention to automated text message reminders see if the adaptive intervention shows stronger positive effects on medication adherence.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SEQUENTIAL
SUPPORTIVE_CARE
NONE
Study Groups
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Adaptive Cell Phone Support
Computer-delivered cell phone support (reminders, problem-solving, referrals to resources) and responsive human coaching (phone calls, test messages, in-app messaging) to improve medication adherence.
Adaptive Cell Phone Support
Mobile health adherence promotion based on the supportive accountability model
Computer-Delivered Cell Phone Support
Mobile health adherence promotion based on the supportive accountability model
Computer-Delivered Cell Phone Support
Computer-delivered cell phone support (reminders, problem-solving, referrals to resources)
Computer-Delivered Cell Phone Support
Mobile health adherence promotion based on the supportive accountability model
Automated Text Reminders
Scheduled one-way text automated message reminders to take medication
Automated Text Reminders
Scheduled text reminder to take medication
Interventions
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Adaptive Cell Phone Support
Mobile health adherence promotion based on the supportive accountability model
Computer-Delivered Cell Phone Support
Mobile health adherence promotion based on the supportive accountability model
Automated Text Reminders
Scheduled text reminder to take medication
Eligibility Criteria
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Inclusion Criteria
* between 15-20 years old
* taking at least one oral medication per day for a chronic health condition
* English speaking
* demonstrating sufficient cognitive capacity to engage in the assent/consent process and study procedures
15 Years
20 Years
ALL
No
Sponsors
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Children's Hospital Los Angeles
OTHER
Responsible Party
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Caitlin Sayegh
Assistant Professor of Clinical Pediatrics
Principal Investigators
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Caitlin Sayegh, PhD
Role: PRINCIPAL_INVESTIGATOR
Children's Hospital Los Angeles
Locations
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Children Hospital Los Angeles
Los Angeles, California, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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CHLA-23-00149_Phase III
Identifier Type: -
Identifier Source: org_study_id
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