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临床试验/NCT07064824
NCT07064824尚未招募不适用

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

Children's Hospital Los Angeles2 个研究点 分布在 1 个国家目标入组 96 人开始时间: 2027年8月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
96
试验地点
2
主要终点
Mean scores on the Mobile Health App Usability Questionnaire

研究概览

简要总结

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.

详细描述

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

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
15 Years 至 20 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 未提供

研究组 & 干预措施

Adaptive Cell Phone Support

Experimental

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.

干预措施: Adaptive Cell Phone Support (Behavioral)

Adaptive Cell Phone Support

Experimental

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.

干预措施: Computer-Delivered Cell Phone Support (Behavioral)

Computer-Delivered Cell Phone Support

Experimental

Computer-delivered cell phone support (reminders, problem-solving, referrals to resources)

干预措施: Computer-Delivered Cell Phone Support (Behavioral)

Automated Text Reminders

Active Comparator

Scheduled one-way text automated message reminders to take medication

干预措施: Automated Text Reminders (Behavioral)

结局指标

主要结局

Mean scores on the Mobile Health App Usability Questionnaire

时间窗: Baseline to 12 weeks

Higher 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 questionnaire

时间窗: Baseline to 12 weeks

Higher 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 Scale

时间窗: Baseline to 12 weeks

Percentage 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 Ruler

时间窗: Baseline to 12 weeks

Higher 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 Questionnaire

时间窗: Baseline to 12 weeks

Higher 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.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Caitlin Sayegh

Assistant Professor of Clinical Pediatrics

Children's Hospital Los Angeles

研究点 (2)

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