Skip to content

Final Prototype Refinement of Adaptive Cell Phone Support

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07084155
Acronym
ACPS
Enrollment
35
Registered
2025-07-24
Start date
2026-03-25
Completion date
2027-01-31
Last updated
2026-07-20

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, adherence

Brief summary

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

Mobile health adherence promotion based on the supportive accountability model

Sponsors

Children's Hospital Los Angeles
Lead SponsorOTHER
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
CollaboratorNIH

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
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 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

.

Design outcomes

Primary

MeasureTime frameDescription
Total scores on the theoretical framework of acceptability questionnaireBaseline to 3 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.
Mean scores on the Mobile Health App Usability QuestionnaireBaseline to 3 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 Visual Analogue ScaleBaseline to 3 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.

Countries

United States

Contacts

CONTACTCaitlin Sayegh, PhD
cssayegh@chla.usc.edu323-361-7748
PRINCIPAL_INVESTIGATORCaitlin Sayegh, PhD

Children's Hospital Los Angeles

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 21, 2026