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| ID | Type | Description | Link |
|---|---|---|---|
| NIDRR grant # H133A070032 | Other Grant/Funding Number | NIDRR |
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| Name | Class |
|---|---|
| U.S. Department of Education | FED |
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This study seeks to determine if problem-based telephone counseling improves quality of life and emotional well-being for caregivers of persons with moderate to severe traumatic brain injury (TBI).
Caregivers and patients with TBI are recruited from the acute medical and inpatient rehabilitation units at Harborview Medical Center and the University of Washington Medical Center in Seattle, WA. After informed consent is obtained, information is gathered from the caregiver about his/her living situation, support systems, and the nature of the caregiving relationship. Additional information is gathered from the person with TBI about how he/she is doing cognitively, socially, and emotionally. Prior to discharge home, caregivers are randomly selected to receive either standard care (typical support and/or resources) or standard care plus problem-based telephone counseling.
The telephone follow-up group receives a telephone call from a caregiver support specialist at 2, 4, 6, 8, 10, 12, 14, and 16 weeks after discharge of the patient with TBI home with the option of two additional calls. During those calls, the caregiver support specialist provides training on problem-solving skills along with education on topics of interest to caregivers of persons with TBI.
An outcome assessment is done at 6 months and 1 year after discharge home.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1: Experimental | Experimental | Problem-solving, education based telephone counseling. |
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| 2: No intervention | Sham Comparator | Standard of care control group |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Problem-solving, education based telephone counseling | Behavioral | Caregivers are contacted every 2 weeks for 16-20 weeks after discharge of TBI survivor home. A caregiver support specialist provides telephone counseling based on a problem-solving, educational model. |
| Measure | Description | Time Frame |
|---|---|---|
| Composite measure based on the Bakas Caregiving Outcomes Scale and the Brief Symptom Inventory | 6 mos and 1 year post discharge home |
| Measure | Description | Time Frame |
|---|---|---|
| Caregiver community participation as measured by the PART-O | 6 mos and 1 year post discharge home | |
| Caregiver employment | 6 mos and 1 year post discharge home | |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Janet M. Powell, PhD | University of Washington | Principal Investigator |
| Kathleen R. Bell, MD | University of Washington | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Washington | Seattle | Washington | 98195 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 27022956 | Derived | Powell JM, Wise EK, Brockway JA, Fraser R, Temkin N, Bell KR. Characteristics and Concerns of Caregivers of Adults With Traumatic Brain Injury. J Head Trauma Rehabil. 2017 Jan/Feb;32(1):E33-E41. doi: 10.1097/HTR.0000000000000219. | |
| 26394294 | Derived | Powell JM, Fraser R, Brockway JA, Temkin N, Bell KR. A Telehealth Approach to Caregiver Self-Management Following Traumatic Brain Injury: A Randomized Controlled Trial. J Head Trauma Rehabil. 2016 May-Jun;31(3):180-90. doi: 10.1097/HTR.0000000000000167. |
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| ID | Term |
|---|---|
| D001930 | Brain Injuries |
| D000070642 | Brain Injuries, Traumatic |
| ID | Term |
|---|---|
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
| D006259 | Craniocerebral Trauma |
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| ID | Term |
|---|---|
| D059039 | Standard of Care |
| ID | Term |
|---|---|
| D019984 | Quality Indicators, Health Care |
| D011787 | Quality of Health Care |
| D006298 | Health Services Administration |
| D017530 | Health Care Quality, Access, and Evaluation |
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| No Intervention | Other | The control group will receive standard of care, i.e., typical resources and/or supports offered to caregivers of persons with TBI. |
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| Caregiver resource utilization |
| 6 mos and 1 year post discharge home |
| Perceived Quality of Life (person with TBI) | 6 mos post discharge home |
| Brief Symptom Inventory (person with TBI) | 6 mos post discharge home |
| D020196 | Trauma, Nervous System |
| D014947 | Wounds and Injuries |