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Completed

NCT Number: NCT02371720

Patient Centered Comprehensive Medication Adherence Management System in Patients With Sickle Cell Disease

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.

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Key information

Age range

2 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Children's National Medical Center, Washington D.C., District of Columbia, United States

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Treatment and study plan

Mobile DOT

Behavioral

Daily reminders via text or email to send a video of themselves taking their Hydroxyurea, positive feedback, and be encouraged to contact the research coordinator with any questions, concerns, etc.

Other names: Comprehensive medication adherence management

Primary outcomes

  1. Medication Possession Ratio (MPR)

    Time frame: 12 months

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

Secondary outcomes

  1. Change in Hemoglobin (Hb) levels

    Time frame: Baseline, 24 months

    Change in hemoglobin levels from baseline to 24 months will be measured using the HemoCue® rapid test.

  2. Change in mean cell volume (MCV)

    Time frame: Baseline, 24 months

    Change from baseline in MCV will be calculated as the value at 24 months minus the value at baseline. MCV is the average size of the red blood cells expressed in femtoliters. MCV is calculated by dividing the hematocrit (as percent) by the red blood cell (RBC) count in millions per microliter of blood, then multiplying by 10.

  3. Change in fetal hemoglobin (HbF) levels

    Time frame: Baseline, 24 months

    Change from baseline in HbF will be calculated as the value at 24 months minus the value at baseline. HbF is expressed as a percentage.

  4. Impact of adherence on clinical outcomes and healthcare utilization

    Time frame: Baseline, 24 months

    Health care utilization in the emergency department and hospitalization due to sickle cell related complications such as vaso-occlusive crisis (VOC) or acute chest syndrome (ACS). Retrospective chart review at baseline will be conducted to determine healthcare utilization.

  5. Impact of adherence on patients' lives

    Time frame: Baseline, 24 months

    Impact of adherence on patients' lives measured using patient reported outcomes (PROMIS), surveys of school attendance, work absenteeism, out-of-pocket costs incurred by patients and their caregivers

  6. Change in adherence with using Mobile-DOT

    Time frame: Baseline, 24 months

    Retrospective chart review at baseline will be conducted to determine medication possession rate (MPR) and then compared to the MPR at 24 months.

  7. Acceptability of intervention and of Hydroxyurea

    Time frame: Baseline, 24 months

    Acceptability will be measured by Treatment Satisfaction Questionnaire for Medication-9 (TSQM-9) The TSQM is a 14-item subject-assessed evaluation of treatment medication including 4 factors, Effectiveness, Side Effects, Convenience, and Global Satisfaction, and it utilizes the following responses on a 7-point Likert scale: 1=Extremely Dissatisfied, 2=Very Dissatisfied, 3=Somewhat Dissatisfied, 4=Neither Satisfied Nor Dissatisfied, 5=Somewhat Satisfied, 6=Very Satisfied, 7=Extremely Satisfied. Scores range from 0-100, with 0 as extremely dissatisfied and 100 as extremely satisfied.

Sponsors and collaborators

Lead sponsor

Emory University

Other

Collaborators

  • Patient-Centered Outcomes Research Institute

Registry information

Official study title

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

Acronym: SCD Mobile Dot

Important dates

Study start
2014
Primary completion
2018
Study completion
2018
First posted
Feb 26, 2015
Registry last updated
Mar 5, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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