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

Primary Purpose

Traumatic Brain Injury

Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Patient-centered in home rehabilitation
Control
Sponsored by
Oslo University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Traumatic Brain Injury focused on measuring Randomized trial,, Health care needs, Traumatic brain injury, Community, Goal attainment

Eligibility Criteria

18 Years - 72 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • OUH

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Patient-centered in home rehabilitation

Control

Arm Description

Eight contacts of about 2 hours duration each delivered over a 4-month period (Six in home visits and two telephone contacts before the Corona pandemic and adjusted to eight contacts and up to six of them video based when necessary during the Corona pandemic) in three phases:

Usual follow-up assessment and health care and rehabilitation services provided in the municipality

Outcomes

Primary Outcome Measures

Participation
Participation assessment and Recombined Tools- Objective (PART-O) (Social domain)
General Health
Quality of Life after Brain Injury (Qolibri overall scale, sum score of 6 items )

Secondary Outcome Measures

Global functioning
Glasgow outcome scale extended (GOSE) (score 0-8)
Depression
Patients Health Questionnaire (PHQ-9) (patients and family members)
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)
Acceptability and satisfaction with the intervention
Acceptability Scale assessed by patients, care providers and family members (sum score)
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.
Symptom burden
Rivermead post-concussion questionnaire (RPQ)(patients) (scoring algoritm)
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
Caregiver burden (Caregiver burden scale)
Caregiver burden-family member
Anxiety Disorder Measurement (GAD-7)
Generalised Anxiety Disorder Measurement (GAD-7) (sumscore 7 items, 0-21)
Participation
Participation assessment and Recombined Tools- Objective (PART-O) (3 domains and total score
General Health
Quality of Life after Brain Injury (Qolibri overall scale, sum score of 6 items )
Participation
Participation assessment and Recombined Tools- Objective (PART-O) (domain Round and about and Productivity, Total score

Full Information

First Posted
May 9, 2018
Last Updated
March 11, 2022
Sponsor
Oslo University Hospital
Collaborators
Sunnaas Rehabilitation Hospital, Virginia Commonwealth University
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1. Study Identification

Unique Protocol Identification Number
NCT03545594
Brief Title
Traumatic Brain Injury; Needs and Treatment Options in the Chronic Phase
Official Title
Traumatic Brain Injury; Needs and Treatment Options in the Chronic Phase. A Randomized Controlled Community-based Intervention
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
June 1, 2018 (Actual)
Primary Completion Date
April 30, 2021 (Actual)
Study Completion Date
December 31, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oslo University Hospital
Collaborators
Sunnaas Rehabilitation Hospital, Virginia Commonwealth University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Traumatic Brain Injury
Keywords
Randomized trial,, Health care needs, Traumatic brain injury, Community, Goal attainment

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled trial
Masking
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.
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Patient-centered in home rehabilitation
Arm Type
Experimental
Arm Description
Eight contacts of about 2 hours duration each delivered over a 4-month period (Six in home visits and two telephone contacts before the Corona pandemic and adjusted to eight contacts and up to six of them video based when necessary during the Corona pandemic) in three phases:
Arm Title
Control
Arm Type
Active Comparator
Arm Description
Usual follow-up assessment and health care and rehabilitation services provided in the municipality
Intervention Type
Other
Intervention Name(s)
Patient-centered in home rehabilitation
Intervention Description
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
Intervention Type
Other
Intervention Name(s)
Control
Intervention Description
Usual follow-up in the municipality
Primary Outcome Measure Information:
Title
Participation
Description
Participation assessment and Recombined Tools- Objective (PART-O) (Social domain)
Time Frame
12 months
Title
General Health
Description
Quality of Life after Brain Injury (Qolibri overall scale, sum score of 6 items )
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Global functioning
Description
Glasgow outcome scale extended (GOSE) (score 0-8)
Time Frame
4 and 12 months
Title
Depression
Description
Patients Health Questionnaire (PHQ-9) (patients and family members)
Time Frame
4 months (patients and family) and 12 months intervention (patients)
Title
Physical and mental health (EQ-5D) and quality-adjusted life years, (QALYs)
Description
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
Title
Acceptability and satisfaction with the intervention
Description
Acceptability Scale assessed by patients, care providers and family members (sum score)
Time Frame
4 and 12 months
Title
Target outcome areas
Description
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
Title
Symptom burden
Description
Rivermead post-concussion questionnaire (RPQ)(patients) (scoring algoritm)
Time Frame
4 and 12 months
Title
Patient and family members, evaluating self-awareness and functioning. Patient and family members, evaluating self-awareness and functioning
Description
Patient Competency Rating Scale (PCRS) (sum score) rated by patient and family member
Time Frame
4 and 12 months
Title
Caregiver burden (Caregiver burden scale)
Description
Caregiver burden-family member
Time Frame
4 and 12 months
Title
Anxiety Disorder Measurement (GAD-7)
Description
Generalised Anxiety Disorder Measurement (GAD-7) (sumscore 7 items, 0-21)
Time Frame
4 and 12 months
Title
Participation
Description
Participation assessment and Recombined Tools- Objective (PART-O) (3 domains and total score
Time Frame
4 months
Title
General Health
Description
Quality of Life after Brain Injury (Qolibri overall scale, sum score of 6 items )
Time Frame
4 months
Title
Participation
Description
Participation assessment and Recombined Tools- Objective (PART-O) (domain Round and about and Productivity, Total score
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
72 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cecilie Røe
Organizational Affiliation
OUH
Official's Role
Study Chair
Facility Information:
Facility Name
OUH
City
Oslo
ZIP/Postal Code
0407
Country
Norway

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Only aggregated data will be shared according to the Norwegian legislation
Citations:
PubMed Identifier
32216840
Citation
Borgen IMH, Lovstad M, Andelic N, Hauger S, Sigurdardottir S, Soberg HL, Sveen U, Forslund MV, Kleffelgard I, Lindstad MO, Winter L, Roe C. Traumatic brain injury-needs and treatment options in the chronic phase: Study protocol for a randomized controlled community-based intervention. Trials. 2020 Mar 27;21(1):294. doi: 10.1186/s13063-020-4195-5.
Results Reference
derived

Learn more about this trial

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

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