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N/A N=67 Randomized Prevention

Using Patient-Centered Guidelines in a Technology Platform to Improve Health Care in Adults With Sickle Cell Disease

Sickle Cell Disease

Enrolled (actual)
67
Serious AEs
0.0%
Results posted
Jun 2024
Primary outcome: Primary: SCD-specific Knowledge — 32.0; 32.0; 33.5; 33 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
mobile health application (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Vanderbilt University Medical Center
Primary completion
Jul 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
SCD-specific Knowledge
32.0; 32.0; 33.5; 33
SECONDARY
Self-efficacy
34.5; 32.5
SECONDARY
Healthcare Utilization (ER Visits and Hospitalizations)
0; 0
SECONDARY
Usage and Usability of the mHealth Application
56.2
SECONDARY
Patient Activation Measure
73.8; 73.8

Summary

SCD is an inherited disorder of hemoglobin that affects over 100,000 Americans, most of whom live in low-resourced neighborhoods. Acute SCD complications result in 230,000 emergency department visits and $1.5 billion annually in acute-care expenditures. Prior research indicates that increased disease-specific knowledge correlates with improved clinical outcomes in SCD. Thus, targeting strategies to improve disease-specific knowledge is a high priority in the care of individuals with SCD. Significant evidence describes how educational materials, including online educational programs, can be used to increase disease-specific knowledge. In this study, the investigators will evaluate a mobile phone technology intervention based on the prior evidence that technologies can improve SCD-specific knowledge.

Eligibility Criteria

Inclusion Criteria

  • receives care at the community health clinic,
  • diagnosis of SCD (Hgb SS, SC, Sβ-thal),
  • ability to speak and understand written English
  • has access to a smartphone or computer
  • between 18-70 years.

Exclusion Criteria

  • lack of access to a smartphone or computer
  • inability to speak and understand written English
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03629678). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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