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Stigma, Self-management, & Quality of Life in SCD

NCT03488264 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 102

Last updated 2019-04-11

No results posted yet for this study

Summary

Many individuals with sickle cell disease experience both a poor quality of life and stigma. Individuals with SCD often experience high levels of stigma which can be a barrier to good self-management and hinder quality of life. The purpose of this research is to improve understanding of the relationships between stigma, self-management, and quality of life in SCD in the United States and Jamaica. The findings from this project will contribute to the development of a tool to measure self-management strategies and will also guide the development of interventions to improve SCD self-management.

Conditions

Sponsors & Collaborators

Principal Investigators

  • Paula Tanabe, PhD · Duke University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-02-13
Primary Completion
2018-10-27
Completion
2018-10-27

Countries

  • United States
  • Jamaica

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03488264 on ClinicalTrials.gov