- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02646176
Comparative Effectiveness of Rehabilitation Interventions for Traumatic Brain Injury (TBI-CER)
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:
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.
- 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.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- 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
- Diagnosed with an International Classification of Diseases (ICD-9-CM) code consistent with the CDC Guidelines for Surveillance of Central Nervous System Injury
- Receiving inpatient care on a designated brain injury rehabilitation unit of one of the participating rehabilitation facilities
- 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 Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Participation
Time Frame: 9 months post-discharge from inpatient rehabilitation
|
Participation as measured by the Participation Assessment with Recombined Tools-Objective
|
9 months post-discharge from inpatient rehabilitation
|
|
Participation
Time Frame: 3 months post-discharge from inpatient rehabilitation
|
Participation as measured by the Participation Assessment with Recombined Tools-Objective
|
3 months post-discharge from inpatient rehabilitation
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional independence-Cognitive
Time Frame: Upon completion of inpatient rehabilitation (discharge score), an average of 1 month
|
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
|
|
Functional independence-Cognitive
Time Frame: 3 months after discharge from inpatient rehabilitation
|
FIM-TM Cognitive scales will be used to measure functional independence in the cognitive realm.
|
3 months after discharge from inpatient rehabilitation
|
|
Functional independence-Cognitive
Time Frame: 9 months after discharge from inpatient rehabilitation
|
FIM-TM Cognitive scales will be used to measure functional independence in the cognitive realm.
|
9 months after discharge from inpatient rehabilitation
|
|
Functional independence-Motor
Time Frame: Upon completion of inpatient rehabilitation (discharge score), an average of 1 month
|
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
|
|
Functional independence-Motor
Time Frame: 3 months post-discharge from inpatient rehabilitation
|
FIM-TM Motor scales will be used to measure functional independence in the cognitive realm.
|
3 months post-discharge from inpatient rehabilitation
|
|
Functional independence-Motor
Time Frame: 9 months post-discharge from inpatient rehabilitation
|
FIM-TM Motor scales will be used to measure functional independence in the cognitive realm.
|
9 months post-discharge from inpatient rehabilitation
|
|
Depressive symptoms
Time Frame: 3 months post-discharge from inpatient rehabilitation
|
The Patient Health Questionnaire-9 will be used to measure depressive symptoms.
|
3 months post-discharge from inpatient rehabilitation
|
|
Depressive symptoms
Time Frame: 9 months post-discharge from inpatient rehabilitation
|
The Patient Health Questionnaire-9 will be used to measure depressive symptoms.
|
9 months post-discharge from inpatient rehabilitation
|
|
Life satisfaction
Time Frame: 3 months post-discharge from inpatient rehabilitation
|
The Satisfaction with Life Scale will be used to measure life satisfaction
|
3 months post-discharge from inpatient rehabilitation
|
|
Life satisfaction
Time Frame: 9 months post-discharge from inpatient rehabilitation
|
The Satisfaction with Life Scale will be used to measure life satisfaction
|
9 months post-discharge from inpatient rehabilitation
|
|
Participation
Time Frame: 3 months post-discharge
|
Participation will be measured using the Participation Assessment with Recombined Tools-Objective
|
3 months post-discharge
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Jennifer A Bogner, PhD, Ohio State University
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- OhioU
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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