跳至主要内容
临床试验/NCT02371720
NCT02371720已完成不适用

Patient Centered Comprehensive Medication Adherence Management System to Improve Effectiveness of Disease Modifying Therapy With Hydroxyurea in Patients With Sickle Cell Disease

Emory University4 个研究点 分布在 1 个国家目标入组 164 人开始时间: 2014年6月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
164
试验地点
4
主要终点
Medication Possession Ratio (MPR)

研究概览

简要总结

The purpose of this research study is to learn about ways to help children and adults with sickle cell disease who are taking the medication, hydroxyurea.

详细描述

Sickle cell disease (SCD) is an inherited chronic multi-organ system disorder that affects approximately 100,000 individuals in the United States, mostly belonging to minority, under-served populations. SCD is associated with substantial morbidity, premature mortality, individual suffering, health care costs and loss of productivity. Hydroxyurea (HU) the only disease modifying therapy for SCD is efficacious in reducing complications such as pain crisis and acute chest syndrome and improving survival. It is however, vastly underutilized and poorly adhered to because of barriers at the health care system, provider, treatment, socioeconomic, and patient levels. The investigator's overarching hypothesis is that barriers to acceptance and adherence to HU are multi-factorial and that a structured set of interventions can lead to improved adherence to medication and patient centered outcomes.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
2 Years 至 65 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •be >2 years of age up to 65 years of age, inclusive
  • •have a diagnosis of SCD, with either βS/βS, βS/βC, βS/βD, βS/β0, βS/βO-Arab, or βS/β+ genotype
  • •prescribed Hydroxyurea for at least the 6 months prior to study entry
  • •have daily access to a smart phone, tablet, personal computer or other device capable of producing and transmitting videos over the internet
  • •be willing and able to record and transmit videos

排除标准

  • •patient or caregiver refuses to take Hydroxyurea as treatment for SCD
  • •diagnosis of significant psychiatric disorder of the subject that could seriously impede the ability to participate in the study
  • •an assessment by the investigator that the subject will not comply with the study procedures outlined in the study protocol
  • •patients receiving automatic home delivery of medications since medication possession ratio is reflective of the patient initiation the refill when they have exhausted the home supply of HU

研究组 & 干预措施

Adults - Mobile DOT

Experimental

Subjects with SCD that are older than 21 years old will receive comprehensive medication adherence management (Mobile DOT) after 1 month assessment period. The subjects will receive the Mobile DOT intervention for 24 months.

干预措施: Mobile DOT (Behavioral)

Adults - standard of care then Mobile DOT

Active Comparator

Subjects with SCD that are older than 21 years old will receive standard of care for the first 12 months. They will then crossover to the comprehensive medication adherence management plan (Mobile DOT) after 1 month assessment period for the remaining 12 months.

干预措施: Mobile DOT (Behavioral)

Children - Mobile DOT

Experimental

Subjects with SCD that are younger than 21 years old will receive comprehensive medication adherence management (Mobile DOT) after 1 month assessment period. The subjects will receive the Mobile DOT intervention for 24 months.

干预措施: Mobile DOT (Behavioral)

Children - standard of care then Mobile DOT

Active Comparator

Subjects with SCD that are younger than 21 years old will receive standard of care for the first 12 months. They will then crossover to the comprehensive medication adherence management plan (Mobile DOT) after 1 month assessment period for the remaining 12 months.

干预措施: Mobile DOT (Behavioral)

结局指标

主要结局

Medication Possession Ratio (MPR)

时间窗: 12 months

Proportion of days the patient is in possession of the medication in the study period

次要结局

  • Change in mean cell volume (MCV)(Baseline, 24 months)
  • Change in fetal hemoglobin (HbF) levels(Baseline, 24 months)
  • Impact of adherence on clinical outcomes and healthcare utilization(Baseline, 24 months)
  • Impact of adherence on patients' lives(Baseline, 24 months)
  • Change in adherence with using Mobile-DOT(Baseline, 24 months)
  • Change in Hemoglobin (Hb) levels(Baseline, 24 months)
  • Acceptability of intervention and of Hydroxyurea(Baseline, 24 months)

研究者

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

Lakshmanan Krishnamurti

Professor

Emory University

研究点 (4)

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