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Traumatic Brain Injury; Needs and Treatment Options in the Chronic Phase

Traumatic Brain Injury; Needs and Treatment Options in the Chronic Phase. A Randomized Controlled Community-based Intervention

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03545594
Enrollment
120
Registered
2018-06-04
Start date
2018-06-01
Completion date
2021-12-31
Last updated
2022-03-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Traumatic Brain Injury

Keywords

Randomized trial,, Health care needs, Traumatic brain injury, Community, Goal attainment

Brief summary

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.

Detailed description

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.

Interventions

OTHERPatient-centered in home rehabilitation

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

OTHERControl

Usual follow-up in the municipality

Sponsors

Sunnaas Rehabilitation Hospital
CollaboratorOTHER
Virginia Commonwealth University
CollaboratorOTHER
Oslo University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Masking description

Independent Outcome Assessor(s) blinded to the intervention arm by masking the ID and randomization arm on the assessment and outcome forms.

Intervention model description

Randomized controlled trial

Eligibility

Sex/Gender
ALL
Age
18 Years to 72 Years
Healthy volunteers
No

Inclusion criteria

* Patients \>16 years at injury and 18-72 years at inclusion, with clinical TBI diagnosis on acute admission and CT/MRI verified injury-related intracranial abnormalities. * Patients reporting TBI-related cognitive, emotional and physical problems and/or reduced physical and mental health and/or difficulties with participation in activities with family, friends and in the community at least 2 years after the injury, * Able to provide informed consent and collaborate in the goal setting processing. * Living at home at study inclusion.

Exclusion criteria

* Patients are excluded if they have severe preexisting neurological disorder that would confound outcome assessments and severe psychiatric diseases * Patients unable to provide informed consent or participate in a goal-setting process. * Participants with insufficient fluency in Norwegian to allow for communication with therapists and outcome assessors will also be excluded. * Substance abuce or history of violence that could represent a security risk for the professionals delivering the intervention

Design outcomes

Primary

MeasureTime frameDescription
Participation12 monthsParticipation assessment and Recombined Tools- Objective (PART-O) (Social domain)
General Health12 monthsQuality of Life after Brain Injury (Qolibri overall scale, sum score of 6 items )

Secondary

MeasureTime frameDescription
Physical and mental health (EQ-5D) and quality-adjusted life years, (QALYs)4 and 12 monthsPhysical and mental health (scored according to the EQ-5D algoritm )and QALYs (patients) and overall health (on a scale 0-100,family members)
Acceptability and satisfaction with the intervention4 and 12 monthsAcceptability Scale assessed by patients, care providers and family members (sum score)
Target outcome areas4 and 12 monthsThe 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.
Symptom burden4 and 12 monthsRivermead post-concussion questionnaire (RPQ)(patients) (scoring algoritm)
Global functioning4 and 12 monthsGlasgow outcome scale extended (GOSE) (score 0-8)
Caregiver burden (Caregiver burden scale)4 and 12 monthsCaregiver burden-family member
Anxiety Disorder Measurement (GAD-7)4 and 12 monthsGeneralised Anxiety Disorder Measurement (GAD-7) (sumscore 7 items, 0-21)
Participation4 monthsParticipation assessment and Recombined Tools- Objective (PART-O) (3 domains and total score
General Health4 monthsQuality of Life after Brain Injury (Qolibri overall scale, sum score of 6 items )
Patient and family members, evaluating self-awareness and functioning. Patient and family members, evaluating self-awareness and functioning4 and 12 monthsPatient Competency Rating Scale (PCRS) (sum score) rated by patient and family member
Depression4 months (patients and family) and 12 months intervention (patients)Patients Health Questionnaire (PHQ-9) (patients and family members)

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026