Skip to content

Development of Quality of Life Tool for TBI

Development of a Quality of Life Tool for Deployment Related TBI

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00714428
Acronym
TBIQOL
Enrollment
485
Registered
2008-07-14
Start date
2009-04-30
Completion date
2012-09-30
Last updated
2015-09-07

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

Conditions

Traumatic Brain Injury

Keywords

Traumatic Brain Injury, Quality of Life

Brief summary

Objectives: The ultimate goal of this research program is to promote seamless, comprehensive care for Operation Enduring Freedom/ Operation Iraqi Freedom (OEF/OIF) veterans. The purpose of this study is to develop a psychometrically sound tool to measure health-related quality of life (HRQOL) applicable to wounded warriors with TBI (deployment-related TBI).

Detailed description

Specific short-term objectives for this study include: O1: Identify a parsimonious set of domains that capture HRQOL in deployment-related TBI. O2: Construct and refine clinically-relevant HRQOL of life item banks for deployment-related TBI, in order to supplement the TBI-QOL and generic Neuro-QOL banks and extend the TBI/Neuro-QOL projects to address the unique issues facing wounded warriors with TBI. O3:Utilize Item Response Theory methodology to refine and calibrate targeted and generic item banks for use with deployment-related TBI. O4:Develop a short form, refining item sets and developing algorithms for future development of a computerized adaptive test. Research Design: The proposed three-year prospective study will employ a mixed methods research design in three stages. Combining qualitative and quantitative methods maximizes the ability of the study team to design and validate a clinically sensitive HRQOL measure for wounded warriors with deployment-related TBI. Furthermore, this approach is consistent with the FDA's draft guidance on patient reported outcome (PRO) measures development. Phase 1: Qualitative data obtained from focus groups of veterans and VA providers will be used to (a) evaluate the generic Neuro-QOL domains and items for relevance and appropriateness for use in deployment-related TBI and (b) identify new HRQOL domains and items specific to deployment-related TBI. \[Objective #1\] Phase 2: The generic and specific item banks will be field tested in a large sample of veterans with deployment-related TBI recruited from all 4 VA Polytrauma Rehabilitation Centers (PRCs). \[Objective #2\] Phase 3: Psychometric analyses, including item response theory (IRT) of field test data will be completed. The psychometric properties of the scale will be evaluated empirically. A short form will be developed, refining item sets and developing algorithms for future development of a computerized adaptive test (CAT). \[Objectives #3 & 4\]

Interventions

None listed

Sponsors

Northwestern University
CollaboratorOTHER
University of Michigan
CollaboratorOTHER
US Department of Veterans Affairs
Lead SponsorFED

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* enrolled in VA and diagnosed with a deployment-related TBI documented in computerized patient record system (CPRS) * at least one year post injury * greater than 18 years of age * able to follow two step commands and * English speaking Clinicians Inclusion Criteria: * Clinicians, including: * physicians * psychologists * nurses * social workers * therapists who have provided care to wounded warriors with deployment-related TBI for at least three years

Exclusion criteria

Veterans

Design outcomes

Primary

MeasureTime frame
development of an outcomes measureone time

Countries

United States

Outcome results

None listed

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