Traumatic brain injury (TBI) is a condition affecting the persons' central nervous system with a need for extensive and highly specialized initial health care provision followed by comprehensive rehabilitation efforts. Frequent and life-long medical, cognitive, emotional and behavioral changes are expected. The community-based services are largely responsible for dealing with the chronic challenges affecting people with TBI. 120 patients \>16 years at the time of injury and between 18 and 72 years at inclusion, with clinical TBI diagnosis on acute admission and verified injury-related intracranial abnormalities reporting cognitive, emotional and physical problems more than 2 years after the injury will be included and randomized to a patient-centered in-home program intervention and treatment as usual. The intervention consists of an individualized and goal-oriented intervention will be provided in the persons' home environment, in close collaboration with family members and local health care providers when available. Assessments will be conducted at baseline, at the end of the intervention 4 months after inclusion and one year after inclusion. Primary outcome is participation (Part-O) and TBI specific health related quality of life (Qolibri). Secondary outcomes include goal attainment within individualized targeted outcome areas, depression and anxiety, symptom burden, unmet health care needs and acceptability of intervention as assessed by patient, family member and health professional. The project will contribute to increased understanding of knowledge transfer processes, and dissemination of evidence based practice for TBI. Thus, the project has the potential to improve the current health care for patients with TBI and its delivery.
Traumatic brain injury (TBI) is a condition affecting the persons' central nervous system with a need for extensive and highly specialized initial health care provision followed by comprehensive rehabilitation efforts. Frequent and life-long medical, cognitive, emotional and behavioral changes are expected. The community-based services are largely responsible for dealing with the chronic challenges affecting people with TBI. 120 patients \>16 years at the time of injury and between 18 and 72 years at inclusion, with clinical TBI diagnosis on acute admission and verified injury-related intracranial abnormalities reporting cognitive, emotional and physical problems more than 2 years after the injury will be included and randomized to a patient-centered in-home program intervention and treatment as usual. The intervention consists of individualized and goal-oriented strategies provided in the persons' home environment in close collaboration with family members and local health care providers. The original protocol describes a total of 8 sessions of which 2 will be telephone based. Due to the Corona pandemic hittting Norway in March 2020 the home visits had to be reduced and adapted to the individual situation of the participants. The protocol now includes 8 sessions with up to 6 of them being delivered by video. The intervention will be provided in addition to the usual treatment the participants receive in the municipality. The control group will receive the usual treatment provided in the municipality. Assessments will be conducted at baseline, at the end of the intervention 4-5 months after inclusion and one year after inclusion. Primary outcome is participation (Part-O) and TBI specific health related quality of life (Qolibri). Secondary outcomes include goal attainment within individualized targeted outcome areas, depression and anxiety, symptom burden, unmet health care needs and acceptability of intervention as assessed by patient, family member and health professional. In March 2020 a few additional questions regarding the impact of the Corona pandemic on health and participation has been included. The closedown periods of the Norwegian Society during Covid-19 will be used as covariate and/or predictors in the analysis. The project will contribute to increased understanding of knowledge transfer processes, and dissemination of evidence based practice for TBI. Thus, the project has the potential to improve the current health care for patients with TBI and its delivery.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Enrollment
120
Eight contacts (six in-home visits of 1-2 hours duration each and two telephone contacts before the Corona pandemic and eight sessions with up to six of them video delivered if necessary during the Corona pandemic ) delivered over a 4-month period in three phases
Usual follow-up in the municipality
OUH
Oslo, Norway
Participation
Participation assessment and Recombined Tools- Objective (PART-O) (Social domain)
Time frame: 12 months
General Health
Quality of Life after Brain Injury (Qolibri overall scale, sum score of 6 items )
Time frame: 12 months
Global functioning
Glasgow outcome scale extended (GOSE) (score 0-8)
Time frame: 4 and 12 months
Depression
Patients Health Questionnaire (PHQ-9) (patients and family members)
Time frame: 4 months (patients and family) and 12 months intervention (patients)
Physical and mental health (EQ-5D) and quality-adjusted life years, (QALYs)
Physical and mental health (scored according to the EQ-5D algoritm )and QALYs (patients) and overall health (on a scale 0-100,family members)
Time frame: 4 and 12 months
Acceptability and satisfaction with the intervention
Acceptability Scale assessed by patients, care providers and family members (sum score)
Time frame: 4 and 12 months
Target outcome areas
The patient nominate their three most important problems and the difficulties they have with them on a scale from 0 to 4. Changes in the difficulty score is evaluated.
Time frame: 4 and 12 months
Symptom burden
Rivermead post-concussion questionnaire (RPQ)(patients) (scoring algoritm)
Time frame: 4 and 12 months
Patient and family members, evaluating self-awareness and functioning. Patient and family members, evaluating self-awareness and functioning
Patient Competency Rating Scale (PCRS) (sum score) rated by patient and family member
Time frame: 4 and 12 months
Caregiver burden (Caregiver burden scale)
Caregiver burden-family member
Time frame: 4 and 12 months
Anxiety Disorder Measurement (GAD-7)
Generalised Anxiety Disorder Measurement (GAD-7) (sumscore 7 items, 0-21)
Time frame: 4 and 12 months
Participation
Participation assessment and Recombined Tools- Objective (PART-O) (3 domains and total score
Time frame: 4 months
General Health
Quality of Life after Brain Injury (Qolibri overall scale, sum score of 6 items )
Time frame: 4 months
Participation
Participation assessment and Recombined Tools- Objective (PART-O) (domain Round and about and Productivity, Total score
Time frame: 12 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.