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Adaptive Cell Phone Support (ACPS)

Adaptive Cell Phone Support to Promote Medication Adherence Among Adolescents and Young Adults With Chronic Health Conditions

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07064824
Acronym
ACPS
Enrollment
96
Registered
2025-07-15
Start date
2027-08-01
Completion date
2030-07-30
Last updated
2025-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Medication Adherence

Keywords

Adolescents, Mobile health, chronic illness

Brief summary

The goal of this pilot clinical trial is to test a mobile health intervention for promoting medication adherence in a population of adolescents and young adults with chronic health conditions. The main question it aims to answer is: -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.

Detailed description

Plan to enroll 96 participants in this study, which is a sequential randomized trial.

Interventions

Mobile health adherence promotion based on the supportive accountability model

BEHAVIORALComputer-Delivered Cell Phone Support

Mobile health adherence promotion based on the supportive accountability model

BEHAVIORALAutomated Text Reminders

Scheduled text reminder to take medication

Sponsors

Children's Hospital Los Angeles
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
15 Years to 20 Years
Healthy volunteers
No

Inclusion criteria

* Children's Hospital Los Angeles patient * 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 There is no

Exclusion criteria

.

Design outcomes

Primary

MeasureTime frameDescription
Mean scores on the Mobile Health App Usability QuestionnaireBaseline to 12 weeksHigher scores indicate greater ease with which users can use technology to achieve a particular goal; the minimum value of this questionnaire is 1 and the maximum value is 7.
Total scores on the theoretical framework of acceptability questionnaireBaseline to 12 weeksHigher scores indicate a greater extent to which people delivering or receiving a healthcare intervention consider it to be appropriate, based on anticipated or experienced cognitive and emotional responses to the intervention; the minimum value of this questionnaire is 7 and the maximum value is 35.
Total scores on the Visual Analogue ScaleBaseline to 12 weeksPercentage of doses taken our of 100%; higher numbers indicate greater medication adherence. This scale presents participants with a line, marked 0 on the left and 100 on the right, and participants can drag a marker to the place on the line that best visually indicated their adherence.
Total scores on Rollnick's Readiness RulerBaseline to 12 weeksHigher scores on this measure indicate more motivation to take medication as prescribed; the minimum value of this questionnaire is 0 and the maximum value is 10.
Total Transition Readiness scores on the Successful Transition to Adulthood with Therapeutic = Rx QuestionnaireBaseline to 12 weeksHigher scores on extent to which patients are prepared to manage their health condition as adults, outside of the pediatric system; ; the minimum value of this questionnaire is 0 and the maximum value is 90.

Countries

United States

Contacts

Primary ContactCaitlin Sayegh, PhD
cssayegh@chla.usc.edu13233617748

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026