Adaptive Cell Phone Support (ACPS)
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Adaptive Cell Phone Support, Computer-Delivered Cell Phone Support, Automated Text Reminders.
- Who it may be relevant to
- Registry conditions: Medication Adherence. Basic parameters: 15 years — 20 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Adaptive Cell Phone Support to Promote Medication Adherence Among Adolescents and Young Adults With Chronic Health Conditions
Overview
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
- Behavioral Adaptive Cell Phone Support
Mobile health adherence promotion based on the supportive accountability model - Behavioral Computer-Delivered Cell Phone Support
Mobile health adherence promotion based on the supportive accountability model - Behavioral Automated Text Reminders
Scheduled text reminder to take medication
Primary outcome measures
- Mean scores on the Mobile Health App Usability Questionnaire [Time frame: Baseline to 12 weeks]
- Total scores on the theoretical framework of acceptability questionnaire [Time frame: Baseline to 12 weeks]
- Total scores on the Visual Analogue Scale [Time frame: Baseline to 12 weeks]
- Total scores on Rollnick's Readiness Ruler [Time frame: Baseline to 12 weeks]
- Total Transition Readiness scores on the Successful Transition to Adulthood with Therapeutic = Rx Questionnaire [Time frame: Baseline to 12 weeks]
Eligibility criteria
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.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Sequential
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
United States · 1 center
- Children Hospital Los Angeles — Los Angeles
Identifiers
NCT: NCT07064824 · CHLA-23-00149_Phase III