Validation of the Sickle Cell Disease Pain Burden Interview
1 other identifier
observational
131
1 country
1
Brief Summary
The purpose of this study is to validate a brief survey tool, the SCD Pain Burden Interview (SCPBI), which can be used in the clinical and/or research settings to assess the impact of pain on children with sickle cell disease.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Dec 2008
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2008
CompletedFirst Submitted
Initial submission to the registry
December 5, 2008
CompletedFirst Posted
Study publicly available on registry
December 8, 2008
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2012
CompletedJuly 30, 2013
July 1, 2013
4 years
December 5, 2008
July 29, 2013
Conditions
Outcome Measures
Primary Outcomes (1)
Correlation with validated measures of pain interference, function, quality of life, and mood.
Quarterly
Eligibility Criteria
Children and adolescents diagnosed with sickle cell disease.
You may qualify if:
- Documented sickle cell disease
- years old or greater
- Primary caregiver present at the first visit for children \< 18 years of age
You may not qualify if:
- Primary language spoken other than English
- Patient is in acute pain episode at time of initial visit
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Connecticut Children's Medical Center
Hartford, Connecticut, 06106, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Director, Pain Relief Program
Study Record Dates
First Submitted
December 5, 2008
First Posted
December 8, 2008
Study Start
December 1, 2008
Primary Completion
December 1, 2012
Study Completion
December 1, 2012
Last Updated
July 30, 2013
Record last verified: 2013-07