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| Name | Class |
|---|---|
| University of California, San Diego | OTHER |
| University of North Carolina, Chapel Hill | OTHER |
| University of Florida | OTHER |
| Moss Rehabilitation Research Institute |
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The goal of this clinical trial is to learn if the Avalon Action Alliance Interdisciplinary Outpatient Rehabilitation Program (IORP) can reduce long-lasting symptoms of traumatic brain injury (TBI) and co-occurring disorders in veterans and first responders. The main questions it aims to answer are:
Researchers will compare the Control group to the Invention group to see if a 3-week of IORP reduced symptoms of TBI and co-occurring disorders in military veterans and first responders.
Participants will complete the following activities. The items with an asterisk(*) are not required or available at all sites.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Interdisciplinary Outpatient Rehabilitation Program Intervention Arm | Other | Participants in this arm will start the 3-Week TBI IORP after baseline evaluation and receiving the recommendation to participate in the IORP. |
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| Control Waiting Period Arm | Other | Participants in this arm will start the 3-Week TBI IORP after observing at least a 3 month waiting period after baseline evaluation and receiving the recommendation to participate in the IORP. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| 3-week interdisciplinary outpatient rehab program (IORP) | Behavioral | Interdisciplinary outpatient rehabilitation program (IORP) for military veterans and first responders experiencing chronic effects of traumatic brain injury (TBI) and co-occurring disorders (e.g., posttraumatic stress disorder, depression, substance use). |
| Measure | Description | Time Frame |
|---|---|---|
| Mean change in Neurobehavioral Symptom Inventory (NSI) | The NSI is a 22-item self-report questionnaire used to assess neurobehavioral symptoms, particularly those following a TBI | Baseline enrollment to 3-month follow-up (post IORP) |
| Measure | Description | Time Frame |
|---|---|---|
| Mean change in Satisfaction with Life Scale (SWLS) | The SWLS is a brief questionnaire used to assess an individual's general satisfaction with their life. It is a self-report scale where participants respond to five statements using a 7-point Likert scale (1 = strongly disagree to 7 = strongly agree) | Baseline enrollment to 3 months post-IORP and 6 months post-IORP |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| BRAVE Program | Milwaukee | Wisconsin | 53226 | United States |
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| OTHER |
| University of Colorado Denver - Anschutz Medical Campus (UCD-AMC) | UNKNOWN |
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| Life Satisfaction Questionnaire (LISAT-11) | LISAT-11 is a brief questionnaire used to assess life satisfaction in life domains such as: vocational, financial and leisure situations, contact with friends, sexual life, self-care management, family life, partner relationship, physical health, and psychological health. | Baseline enrollment to 3 months post-IORP and 6 months post-IORP |
| Participation Assessment with Recombined Tools-Objective (PART-O) | The PART-O measures an individual's engagement in everyday life across 17 items spanning three domains: Productivity, Social Relations, and Out and About. The PART-O was developed to examine long-term outcomes and can also be used to evaluate the effectiveness of rehabilitative interventions to improve social/societal functioning. | Baseline enrollment to 3 months post-IORP and 6 months post-IORP |
| ID | Term |
|---|---|
| D000070642 | Brain Injuries, Traumatic |
| ID | Term |
|---|---|
| D001930 | Brain Injuries |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
| D006259 | Craniocerebral Trauma |
| D020196 | Trauma, Nervous System |
| D014947 | Wounds and Injuries |
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