Comparative Effectiveness of Rehabilitation Interventions for Traumatic Brain Injury (TBI-CER)

October 20, 2021 updated by: Jennifer Bogner, PhD, ABPP

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.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

2130

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

The study sample was drawn from the population of persons who received inpatient rehabilitation for TBI in North America.

Description

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 Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jennifer A Bogner, PhD, Ohio State University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

October 1, 2008

Primary Completion (Actual)

October 1, 2012

Study Completion (Actual)

October 1, 2012

Study Registration Dates

First Submitted

December 30, 2015

First Submitted That Met QC Criteria

December 31, 2015

First Posted (Estimate)

January 5, 2016

Study Record Updates

Last Update Posted (Actual)

October 28, 2021

Last Update Submitted That Met QC Criteria

October 20, 2021

Last Verified

October 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

A complete de-identified dataset will be made available to the public within 9 months of completion of the analysis.

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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