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Multidisciplinary Treatment in Patients With Mild Traumatic Brain Injury

Effect of Multidisciplinary Treatment in Patients With Mild Traumatic Brain Injury - a Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00869154
Enrollment
151
Registered
2009-03-25
Start date
2009-03-01
Completion date
2015-03-31
Last updated
2017-08-14

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

Conditions

Traumatic Brain Injury With Brief Loss of Consciousness

Keywords

Mild TBI, TBI (Traumatic Brain Injury), Traumatic Brain Injury, Injury, Brain, Traumatic, Injuries, Acute Brain, Brain Injuries, Traumatic, Acute Brain Injuries

Brief summary

The aim of the study is to compare a multidisciplinary examination and follow up by rehabilitation program with a multidisciplinary examination, good advice and follow up by the family doctor. Further on we will examine if there were differing clinical characteristics between patients who attended a planned follow-up session and those that failed to and Prognostic factors in mild traumatic brain injury patients after discharge from hospital.

Detailed description

2 months after an acute mild traumatic brain injury (TBI) defined as Glasgow Coma Scale between 13 and 15. The patient will get a clinical examination by a specialist in rehabilitation medicine. Patient who wish or need a further follow up, are out of work or school, will be included and randomized to either a multidisciplinary follow up or primary care follow by their family doctor. Both groups will got a multidisciplinary examination. The multidisciplinary team will work out a rehabilitation program and a report back to their family doctor. Patient who got a multidisciplinary follow up will then get individual appointments and they will follow an educational program for 4 days. The topics are physical and psychical problems after TBI and problems in daily living and return to work. We will teach a way to accept and deal with their problems. A cognitive behavioural treatment or a psycho educative approach will be central in the treatment. The follow up period will be until 2 years if needed. For booth groups we will make a registration of sick leave for 5 years. The Extended Glasgow Outcome Scale (GOS- E), Hospital Anxiety and Depression Scale (HAD), Rivermead post concussion symptoms questionnaire and Patient Global Impression of Change (PGIC) after 6 and 12 months. Department of Economics at the University of Bergen will make cost-benefit analysis. Further on we will examine if there were differing clinical characteristics between patients who attended a planned follow-up session and those that failed to, if sick leave or return to work could make a difference and Prognostic factors in mild traumatic brain injury patients after discharge from hospital. We also include demographic data, CT findings and clinical data based on information from the medical records, pain drawings and numeric rating scale for pain, Quality of Life and Subjective Health Complaints inventory. We got data about days on sick leave, diagnosis for sick leave and income for the first year before and after the injury from The Norwegian Labour and Welfare Service (NAV) through a third accredited agency Statistics Norway. From Statistics Norway we got additional information about education level and income.

Interventions

BEHAVIORALprimary care follow up

Multidisciplinary examination, good advice from rehabilitation specialists and follow up by the family doctor.

BEHAVIORALMultidisciplinary follow up

Multidisciplinary examination and follow up by rehabilitation specialists, a multidisciplinary team following an individual rehabilitation programs.

Sponsors

Stiftelsen Helse og Rehabilitering
CollaboratorOTHER
Ullevaal University Hospital
CollaboratorOTHER
Haukeland University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Masking description

The baseline data were collected before randomization. The data collection at 12 months was conducted by postal self-report questionnaires, and for GOSE, an assistant who was blinded to the group allocation performed a telephone interview. Two independent persons, who were blinded for the groups and were unfamiliar with the aim and content of the study, entered the data into the SPSS database. A statistician, who did not participate in the treatment program and was blinded to the group allocation when the data were analyzed, controlled the data and performed the statistical analyses for RTW and the secondary outcomes.

Intervention model description

Randomized controlled trial. Multidisciplinary outpatient rehabilitation with individual contacts and a psycho-educational group intervention at two outpatient rehabilitation clinics compared to follow-up by a general practitioner after a multidisciplinary examination.

Eligibility

Sex/Gender
ALL
Age
16 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* Patient admitted acute to Department of Neurosurgery ICD-10 diagnosed S06.0- S06.9 * Age 16 to 55 years * Mild traumatic brain injury defined as Glasgow Coma Scale (GCS) between 13 and 15.

Exclusion criteria

* Earlier severe traumatic brain injury (GCS 8 or less). * Serious psychiatric disease (ICD-10 diagnosed last two years). * Known drug abuse (ICD-10 diagnosed last two years). * Other serious illness which have a major impact of the outcome. * Social client last two years as major income

Design outcomes

Primary

MeasureTime frameDescription
Return to work6 and 12 months after 1. multidisciplinary examinationSick leave for 5 years after injury

Secondary

MeasureTime frameDescription
GOSE6 and 12 months after 1. multidisciplinary examinationGlasgow Outcome Scale Extended
Post-commotio symptoms (RPQ)12 monthsThe Rivermead Post concussion symptoms Questionnaire
Patient's Global Impression of Change12 monthsPatient's Global Impression of Change

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026