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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02371720
Acronym
SCD Mobile Dot
Enrollment
164
Registered
2015-02-26
Start date
2014-06-01
Completion date
2018-12-31
Last updated
2021-03-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sickle Cell Disease

Brief summary

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.

Detailed description

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.

Interventions

BEHAVIORALMobile DOT

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.

Sponsors

Patient-Centered Outcomes Research Institute
CollaboratorOTHER
Emory University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
2 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Medication Possession Ratio (MPR)12 monthsProportion of days the patient is in possession of the medication in the study period

Secondary

MeasureTime frameDescription
Change in mean cell volume (MCV)Baseline, 24 monthsChange 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.
Change in fetal hemoglobin (HbF) levelsBaseline, 24 monthsChange from baseline in HbF will be calculated as the value at 24 months minus the value at baseline. HbF is expressed as a percentage.
Impact of adherence on clinical outcomes and healthcare utilizationBaseline, 24 monthsHealth 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.
Change in Hemoglobin (Hb) levelsBaseline, 24 monthsChange in hemoglobin levels from baseline to 24 months will be measured using the HemoCue® rapid test.
Change in adherence with using Mobile-DOTBaseline, 24 monthsRetrospective chart review at baseline will be conducted to determine medication possession rate (MPR) and then compared to the MPR at 24 months.
Acceptability of intervention and of HydroxyureaBaseline, 24 monthsAcceptability 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.
Impact of adherence on patients' livesBaseline, 24 monthsImpact 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

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026