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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02646176
Other study ID # OhioU
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 2008
Est. completion date October 2012

Study information

Verified date October 2021
Source Ohio State University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Traumatic brain injury (TBI) is increasingly recognized as a significant public health issue, but the most effective rehabilitation methods have yet to be identified. The Institute of Medicine and the Agency for Healthcare Quality and Research sponsored systematic reviews of evidence for comparative effectiveness of rehabilitation interventions for TBI. Both reviews concluded that substantially more research is needed to identify interventions best suited for different individuals. The practice-based evidence (PBE) approach employed to create the data used in the proposed study was a research method recommended to provide greater clarity, along with use of patient-centered outcomes obtained over a longer period of time than used in previous studies. The following specific aims will be addressed in the proposed study: 1. Determine the comparative effectiveness of different therapeutic approaches used in inpatient TBI rehabilitation after statistically adjusting for patient need and ability to benefit from various approaches. Investigators hypothesize: 1.1. Patients who receive a greater proportion of therapy time in Advanced Training (versus Standard of Care) will achieve better outcomes than similar patients who receive a lesser proportion of treatment time in Advanced Training. 1.2. Patients with the greatest initial levels of disability will experience larger effects from Advanced Training therapeutic approaches in comparison to the effects experienced by patients with less disability at admission. 1.3. Patients who receive a greater proportion of therapy in contextualized treatment (versus decontextualized) will achieve better outcomes than similar patients who receive a lesser proportion of time in contextualized treatment. 2. Determine the comparative effectiveness of difference in the delivery of inpatient rehabilitation therapies, after statistically adjusting for patient need and ability to benefit. Investigators hypothesize: 2.1 The level of effort that patients are able to apply in treatment moderates the effectiveness of time in treatment. 2.2 Family involvement in treatment is associated with better outcomes. Data will be drawn from the database established for the TBI Practice-Based Evidence Study (TBI-PBE Study). Data on 2130 persons who received inpatient TBI rehabilitation at any of 10 sites (9 in US, 1 in Canada) were obtained for the study. Detailed longitudinal data were collected prospectively on rehabilitation therapies (with point of care data completed for every clinical encounter), course of recovery, person and injury characteristics and outcomes during and after rehabilitation. Advanced analytic methods (e.g. propensity scores, generalized linear mixed models) will be used to compare the effects of different rehabilitation interventions on outcomes at discharge and during the 9 months following rehabilitation.


Recruitment information / eligibility

Status Completed
Enrollment 2130
Est. completion date October 2012
Est. primary completion date October 2012
Accepts healthy volunteers No
Gender All
Age group 14 Years and older
Eligibility Inclusion Criteria: 1. Sustained a TBI, defined as damage to brain tissue caused by external force and evidenced by loss of consciousness, post-traumatic amnesia, skull fracture, or objective neurological findings 2. Diagnosed with an International Classification of Diseases (ICD-9-CM) code consistent with the CDC Guidelines for Surveillance of Central Nervous System Injury 3. Receiving inpatient care on a designated brain injury rehabilitation unit of one of the participating rehabilitation facilities 4. Incurred a TBI severe enough to warrant inpatient rehabilitation regardless of other injuries, with TBI being the predominant reason for rehabilitation admission Exclusion Criteria: 1. None

Study Design


Intervention

Behavioral:
Inpatient rehabilitation
Inpatient rehabilitation includes activities and interventions provided by occupational, physical, therapeutic recreation and speech therapists, and psychologists.

Locations

Country Name City State
n/a

Sponsors (3)

Lead Sponsor Collaborator
Jennifer Bogner, PhD, ABPP Patient-Centered Outcomes Research Institute, University of Utah

Outcome

Type Measure Description Time frame Safety issue
Primary Participation Participation as measured by the Participation Assessment with Recombined Tools-Objective 9 months post-discharge from inpatient rehabilitation
Primary Participation Participation as measured by the Participation Assessment with Recombined Tools-Objective 3 months post-discharge from inpatient rehabilitation
Secondary Functional independence-Cognitive FIM-TM Cognitive scales will be used to measure functional independence in the cognitive realm. Upon completion of inpatient rehabilitation (discharge score), an average of 1 month
Secondary Functional independence-Cognitive FIM-TM Cognitive scales will be used to measure functional independence in the cognitive realm. 3 months after discharge from inpatient rehabilitation
Secondary Functional independence-Cognitive FIM-TM Cognitive scales will be used to measure functional independence in the cognitive realm. 9 months after discharge from inpatient rehabilitation
Secondary Functional independence-Motor FIM-TM Motor scales will be used to measure functional independence in the cognitive realm. Upon completion of inpatient rehabilitation (discharge score), an average of 1 month
Secondary Functional independence-Motor FIM-TM Motor scales will be used to measure functional independence in the cognitive realm. 3 months post-discharge from inpatient rehabilitation
Secondary Functional independence-Motor FIM-TM Motor scales will be used to measure functional independence in the cognitive realm. 9 months post-discharge from inpatient rehabilitation
Secondary Depressive symptoms The Patient Health Questionnaire-9 will be used to measure depressive symptoms. 3 months post-discharge from inpatient rehabilitation
Secondary Depressive symptoms The Patient Health Questionnaire-9 will be used to measure depressive symptoms. 9 months post-discharge from inpatient rehabilitation
Secondary Life satisfaction The Satisfaction with Life Scale will be used to measure life satisfaction 3 months post-discharge from inpatient rehabilitation
Secondary Life satisfaction The Satisfaction with Life Scale will be used to measure life satisfaction 9 months post-discharge from inpatient rehabilitation
Secondary Participation Participation will be measured using the Participation Assessment with Recombined Tools-Objective 3 months post-discharge
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