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CompletedNCT00714428TBIQOLUpdated Sep 7, 2015

Development of Quality of Life Tool for TBI

An observational study in Traumatic Brain Injury, sponsored by US Department of Veterans Affairs. Completed at 4 sites in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2015-09-07.

Sponsored by US Department of Veterans Affairs · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
485
Ages
18 Years and older
Sex
All
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Study 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).

Read the 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 Furthermore, this approach is consistent with the FDA's draft guidance on patient reported outcome (PRO) measures development.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]

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Conditions studied

  • Traumatic Brain Injury

Keywords

  • Traumatic Brain Injury
  • Quality of Life
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In context

Brain Injuries, Traumatic

1,818 studies on the registry are indexed under Brain Injuries, Traumatic; 460 are open to participants now.

This study's enrollment of 485 is above the median of 119 across 579 observational studies indexed under Brain Injuries, Traumatic.

Browse Brain Injuries, Traumatic studies →

Lead sponsor

US Department of Veterans Affairs is the lead sponsor of 675 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Individuals with deployment related traumatic brain injury and clinicians who treat those veterans.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

Veterans Exclusion criteria include:

  • those veterans who are not yet discharged from initial rehabilitation (want patients to experience community based living environment)
  • living in the community less than three months post initial rehabilitation, including residential care or long term care living environments

No exclusion criteria for the clinicians

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Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
485 participants (actual)
Biospecimen retention
None retained

Groups and cohorts

  • Group 1: Item Development

    Individuals with TBI to provide input to relevant questions for quality of life measure in TBI

  • Group 2: Item Development

    Clinicians who treat those with deployment related TBI to obtain their feedback on relevant questions pertaining to quality of life measures in TBI.

  • Group 3: Instrument Development

    Individuals with deployment TBI who will complete the Beta version of the TBI QOL measure.

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What researchers measure

Primary outcomes

  1. development of an outcomes measure

    Time frame: one time

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Study locations

4 sites
  • VA Palo Alto Health Care System
    Palo Alto, California 94304-1290, United States
  • James A. Haley Veterans' Hospital
    Tampa, Florida 33612-4745, United States
  • VA Medical Center, Minneapolis
    Minneapolis, Minnesota 55417, United States
  • Hunter Holmes McGuire VA Medical Center
    Richmond, Virginia 23249, United States
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References and documents

Publications

  • Toyinbo PA, Vanderploeg RD, Donnell AJ, Mutolo SA, Cook KF, Kisala PA, Tulsky DS. Development and Initial Validation of Military Deployment-Related TBI Quality-of-Life Item Banks. J Head Trauma Rehabil. 2016 Jan-Feb;31(1):52-61. doi: 10.1097/HTR.0000000000000089. PubMed 25310294 ↗
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Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Apr 2009, a primary completion of Dec 2011 and a completion of Sep 2012. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 8, 2008
First posted
Jul 14, 2008
Start
Apr 2009
Primary completionActual
Dec 2011
CompletionActual
Sep 2012
Last update
Sep 7, 2015
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 7, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00714428
Responsible party
Sponsor
First posted
Jul 14, 2008
Start date
Apr 2009
Primary completion
Dec 2011
Completion
Sep 2012
Last update
Sep 7, 2015

Study contacts

Rodney D Vanderploeg, PhD
principal investigator · James A. Haley Veterans' Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2015. You cannot join it, but the record below documents what was studied.

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