Final Prototype Refinement of Adaptive Cell Phone Support
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.
- 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 →
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Official title
Adaptive Cell Phone Support to Promote Medication Adherence Among Adolescents and Young Adults With Chronic Health Conditions
Overview
The goal of this feasibility pilot trial is to finalize the design of a mobile health intervention for promoting medication adherence in a population of adolescents and young adults with chronic health conditions. The main question\[s\] it aims to answer are: 1. Is the final version of the intervention sufficiently feasible, usable, and acceptable for evaluation in a randomized clinical trial? 2. Do participants show improvements in medication adherence during their field testing of the intervention?
Detailed description
Adolescents with chronic health conditions will be asked to try the intervention for three weeks and give feedback to refine the structure and content in preparation for a future randomized trial of the finalized version of the intervention. Plan to enroll 35 participants in this single arm feasibility/usability trial.
Interventions
- Behavioral Adaptive Cell Phone Support
Mobile health adherence promotion based on the supportive accountability model
Primary outcome measures
- Total scores on the theoretical framework of acceptability questionnaire [Time frame: Baseline to 3 weeks]
- Mean scores on the Mobile Health App Usability Questionnaire [Time frame: Baseline to 3 weeks]
- Total scores on the Visual Analogue Scale [Time frame: Baseline to 3 weeks]
Eligibility criteria
Inclusion criteria
- Children's Hospital Los Angeles patient
- between 15-20 years old at enrollment
- 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
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
United States · 1 center
- Children's Hospital Los Angeles — Los Angeles
Identifiers
NCT: NCT07084155 · CHLA-23-00149_Phase II · 1K23HD119369