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Validation of the Sickle Cell Disease Pain Burden Interview

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00804362
Enrollment
131
Registered
2008-12-08
Start date
2008-12-31
Completion date
2012-12-31
Last updated
2013-07-30

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

Conditions

Pain, Sickle Cell Disease

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.

Interventions

None listed

Sponsors

Connecticut Children's Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
7 Years to 21 Years
Healthy volunteers
No

Inclusion criteria

* Documented sickle cell disease * 7 years old or greater * Primary caregiver present at the first visit for children \< 18 years of age

Exclusion criteria

* Primary language spoken other than English * Patient is in acute pain episode at time of initial visit

Design outcomes

Primary

MeasureTime frame
Correlation with validated measures of pain interference, function, quality of life, and mood.Quarterly

Countries

United States

Outcome results

None listed

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