Telephone Intervention for Caregivers of Persons With Traumatic Brain Injury
|Brain Injuries||Behavioral: Problem-solving, education based telephone counseling Other: No Intervention||Phase 2|
|Study Design:||Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Treatment
|Official Title:||Modular Scheduled Telephone Intervention for Caregivers of Persons With Traumatic Brain Injury: A Randomized Controlled Trial|
- Composite measure based on the Bakas Caregiving Outcomes Scale and the Brief Symptom Inventory [ Time Frame: 6 mos and 1 year post discharge home ]
- Caregiver community participation as measured by the PART-O [ Time Frame: 6 mos and 1 year post discharge home ]
- Caregiver employment [ Time Frame: 6 mos and 1 year post discharge home ]
- Caregiver resource utilization [ Time Frame: 6 mos and 1 year post discharge home ]
- Perceived Quality of Life (person with TBI) [ Time Frame: 6 mos post discharge home ]
- Brief Symptom Inventory (person with TBI) [ Time Frame: 6 mos post discharge home ]
|Study Start Date:||June 2008|
|Study Completion Date:||April 2013|
|Primary Completion Date:||September 2012 (Final data collection date for primary outcome measure)|
Experimental: 1: Experimental
Problem-solving, education based telephone counseling.
Behavioral: Problem-solving, education based telephone counseling
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.
Sham Comparator: 2: No intervention
Standard of care control group
Other: No Intervention
The control group will receive standard of care, i.e., typical resources and/or supports offered to caregivers of persons with TBI.
Other Name: Standard of care
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.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00692575
|United States, Washington|
|University of Washington|
|Seattle, Washington, United States, 98195|
|Principal Investigator:||Janet M. Powell, PhD||University of Washington|
|Study Director:||Kathleen R. Bell, MD||University of Washington|