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Get Going After concussioN 2.0 (GAIN2)

Primary Purpose

Commotio Cerebri, Mild Traumatic Brain Injury

Status
Active
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
GAIN 2.0
Sponsored by
University of Aarhus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Commotio Cerebri

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Concussion caused by a head trauma according to the diagnostic criteria recommended by WHO. Participants must be referred to the project within two to four months of injury.
  2. Age 18 to 60 years at the time of the trauma
  3. A RPQ score ≥20.
  4. Able to understand, speak and read Danish.
  5. Living in Central Denmark Region.

Exclusion Criteria:

  1. Objective neurological findings and/or acute trauma CT scan indicating neurological disease or brain damage.
  2. Previous concussion leading to persistent PCS within the last two years.
  3. Severe misuse of alcohol, prescription drugs and/or illegal drugs.
  4. Psychiatric morbidity or severe neurological disease that impedes participation in the program, i.e. Bipolar Disorder, autism, psychotic disorder (life time), multiple sclerosis etc.

Sites / Locations

  • Regionshospitalet Hammel Neurocenter

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Enhanced usual care

GAIN 2.0 intervention

Arm Description

Participants will be informed about typical Post Concussion Symptoms and the process of typical recovery as well as given reassurance concerning the prognosis. Advice concerning the use of pain relief medication will also be provided.

An eight-week, interdisciplinary intervention program based on principles from cognitive behavioural therapy (CBT) and gradual return to activities.

Outcomes

Primary Outcome Measures

Change of at least seven in the sum score on the Rivermead Post-Concussion Symptoms Questionnaire (RPQ)
RPQ is a self-report scale to measure the severity of Post Concussion Symptoms covering physical, cognitive, and emotional symptoms with 16 sub-items and a total sum score (range 0-64, higher score define more severe status)

Secondary Outcome Measures

Sumscore in the dimension 'time spend on daily activities' on the Utrecht Scale for Evaluation of Rehabilitation-Participation (USER-P).
Utrecht Scale for Evaluation of Rehabilitation-Participation is a generic measurement that both objectively and subjectively measure participation in Instrumental Activities of Daily Living (IADL) such as work, voluntary work, education, family duties and responsibilities, leisure activities, transportation, communication and social activities in three dimensions. The sumscore in each dimension is converted to a 0-100 metric with higher scores meaning af better outcome.
Sumscore in the dimension 'limitations' on the Utrecht Scale for Evaluation of Rehabilitation-Participation (USER-P)
Utrecht Scale for Evaluation of Rehabilitation-Participation is a generic measurement that both objectively and subjectively measure participation in Instrumental Activities of Daily Living (IADL) such as work, voluntary work, education, family duties and responsibilities, leisure activities, transportation, communication and social activities in three dimensions.The sumscore in each dimension is converted to a 0-100 metric with higher scores meaning af better outcome.
Sumscore in the dimension 'satisfaction with participation' on the Utrecht Scale for Evaluation of Rehabilitation-Participation (USER-P)
Utrecht Scale for Evaluation of Rehabilitation-Participation is a generic measurement that both objectively and subjectively measure participation in Instrumental Activities of Daily Living (IADL) such as work, voluntary work, education, family duties and responsibilities, leisure activities, transportation, communication and social activities in three dimensions.The sumscore in each dimension is converted to a 0-100 metric with higher scores meaning af better outcome.
Long term sick leave defined as public assistance benefits related to illness in more than three consecutive weeks
Calculated based on weekly public assistance benefits extracted from the DREAM register
Cumulated incidence proportion of participants on long term sick leave defined as receiving public assistance benefits related to illness in more than three consecutive weeks
Calculated based on weekly public assistance benefits extracted from the DREAM register
Proportion of employed participants defined as receiving no public assistance benefits except from state education fund grants
Calculated based on weekly public assistance benefits extracted from the DREAM register
Proportion of employed participants defined as receiving no public assistance benefits except from state education fund grants
Calculated based on weekly public assistance benefits extracted from the DREAM register
Degree of job stability based on whether labor market contributions have been paid
Monthly measure extracted from the DREAM register
Degree of job stability based on whether labor market contributions have been paid
Monthly measure extracted from the DREAM register

Full Information

First Posted
March 9, 2021
Last Updated
November 2, 2022
Sponsor
University of Aarhus
Collaborators
Sygeforsikringen danmark, Hammel Neurorehabilitation Centre and University Research Clinic, Municipalities in Central Denmark Region
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1. Study Identification

Unique Protocol Identification Number
NCT04798885
Brief Title
Get Going After concussioN 2.0
Acronym
GAIN2
Official Title
Interdisciplinary Intervention for Patients With Post-concussion Symptoms 3-6 Months Post-injury (GAIN 2.0). A Stepped Wedge Cluster Randomised Trial: Effect on Symptoms, Participation in Daily Activities, and Labour Market Attachment
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
May 12, 2021 (Actual)
Primary Completion Date
February 2023 (Anticipated)
Study Completion Date
March 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus
Collaborators
Sygeforsikringen danmark, Hammel Neurorehabilitation Centre and University Research Clinic, Municipalities in Central Denmark Region

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
The study tests the promising results of a previous study (GAIN 1.0) in a larger RCT (GAIN 2.0) which takes place in the municipalities of Central Denmark Region where citizens live their daily lives and whose health- and social care systems support citizens who experience persisting PCS.
Detailed Description
Concussion, the mildest form of traumatic brain injury, is an important public health concern. Recent studies estimate that persistent post-concussion symptoms (PCS) are present in almost half of the affected citizens at one year post-injury. Prospective studies have demonstrated that these citizens are at risk of developing long-lasting symptoms which are associated with high societal burden due to long-term impact on labour market attachment and increased use of health care and social benefits. In Denmark, there has in recent years been an increasing awareness on societal impact and personal consequences of PCS. Accordingly, clinicians as well as social workers and therapists in the municipalities point to the gab in knowledge concerning PCS and advocate urgently for evidence-based treatment for these citizens. Recently, the research group behind this application developed a novel early intervention - "Get going After concussIoN" (GAIN 1.0) - for citizens who experience persistent PCS three to six months post-concussion. The intervention was tested in a randomized controlled trial (RCT) with promising results. However, it was delivered in a single hospital setting in which these citizens are normally not cared for. In this study the intention is to test the results of GAIN 1.0 in a larger RCT (GAIN 2.0) which takes place in the municipalities of Central Denmark Region where citizens live their daily lives and whose health- and social care systems support citizens who experience persisting PCS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Commotio Cerebri, Mild Traumatic Brain Injury

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
310 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Enhanced usual care
Arm Type
No Intervention
Arm Description
Participants will be informed about typical Post Concussion Symptoms and the process of typical recovery as well as given reassurance concerning the prognosis. Advice concerning the use of pain relief medication will also be provided.
Arm Title
GAIN 2.0 intervention
Arm Type
Experimental
Arm Description
An eight-week, interdisciplinary intervention program based on principles from cognitive behavioural therapy (CBT) and gradual return to activities.
Intervention Type
Behavioral
Intervention Name(s)
GAIN 2.0
Intervention Description
1) three structured group sessions of two hours duration performed jointly by a neuropsychologist, an occupational therapist and a physiotherapist. Relatives are also invited. 2) Up to five weekly semi-structured individual sessions of 30 min. duration with an allocated therapist
Primary Outcome Measure Information:
Title
Change of at least seven in the sum score on the Rivermead Post-Concussion Symptoms Questionnaire (RPQ)
Description
RPQ is a self-report scale to measure the severity of Post Concussion Symptoms covering physical, cognitive, and emotional symptoms with 16 sub-items and a total sum score (range 0-64, higher score define more severe status)
Time Frame
Three months after end of treatment
Secondary Outcome Measure Information:
Title
Sumscore in the dimension 'time spend on daily activities' on the Utrecht Scale for Evaluation of Rehabilitation-Participation (USER-P).
Description
Utrecht Scale for Evaluation of Rehabilitation-Participation is a generic measurement that both objectively and subjectively measure participation in Instrumental Activities of Daily Living (IADL) such as work, voluntary work, education, family duties and responsibilities, leisure activities, transportation, communication and social activities in three dimensions. The sumscore in each dimension is converted to a 0-100 metric with higher scores meaning af better outcome.
Time Frame
Three months after end of treatment
Title
Sumscore in the dimension 'limitations' on the Utrecht Scale for Evaluation of Rehabilitation-Participation (USER-P)
Description
Utrecht Scale for Evaluation of Rehabilitation-Participation is a generic measurement that both objectively and subjectively measure participation in Instrumental Activities of Daily Living (IADL) such as work, voluntary work, education, family duties and responsibilities, leisure activities, transportation, communication and social activities in three dimensions.The sumscore in each dimension is converted to a 0-100 metric with higher scores meaning af better outcome.
Time Frame
Three months after end of treatment
Title
Sumscore in the dimension 'satisfaction with participation' on the Utrecht Scale for Evaluation of Rehabilitation-Participation (USER-P)
Description
Utrecht Scale for Evaluation of Rehabilitation-Participation is a generic measurement that both objectively and subjectively measure participation in Instrumental Activities of Daily Living (IADL) such as work, voluntary work, education, family duties and responsibilities, leisure activities, transportation, communication and social activities in three dimensions.The sumscore in each dimension is converted to a 0-100 metric with higher scores meaning af better outcome.
Time Frame
Three months after end of treatment
Title
Long term sick leave defined as public assistance benefits related to illness in more than three consecutive weeks
Description
Calculated based on weekly public assistance benefits extracted from the DREAM register
Time Frame
Within 12 months after concussion
Title
Cumulated incidence proportion of participants on long term sick leave defined as receiving public assistance benefits related to illness in more than three consecutive weeks
Description
Calculated based on weekly public assistance benefits extracted from the DREAM register
Time Frame
Within 36 months after concussion
Title
Proportion of employed participants defined as receiving no public assistance benefits except from state education fund grants
Description
Calculated based on weekly public assistance benefits extracted from the DREAM register
Time Frame
At 12 months after concussion
Title
Proportion of employed participants defined as receiving no public assistance benefits except from state education fund grants
Description
Calculated based on weekly public assistance benefits extracted from the DREAM register
Time Frame
At 36 months after concussion
Title
Degree of job stability based on whether labor market contributions have been paid
Description
Monthly measure extracted from the DREAM register
Time Frame
At 12 months after concussion
Title
Degree of job stability based on whether labor market contributions have been paid
Description
Monthly measure extracted from the DREAM register
Time Frame
At 36 months after concussion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Concussion caused by a head trauma according to the diagnostic criteria recommended by WHO. Participants must be referred to the project within two to four months of injury. Age 18 to 60 years at the time of the trauma A RPQ score ≥20. Able to understand, speak and read Danish. Living in Central Denmark Region. Exclusion Criteria: Objective neurological findings and/or acute trauma CT scan indicating neurological disease or brain damage. Previous concussion leading to persistent PCS within the last two years. Severe misuse of alcohol, prescription drugs and/or illegal drugs. Psychiatric morbidity or severe neurological disease that impedes participation in the program, i.e. Bipolar Disorder, autism, psychotic disorder (life time), multiple sclerosis etc.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jørgen F Nielsen, Professor
Organizational Affiliation
Hammel Neurorehabilitation Centre and University clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Regionshospitalet Hammel Neurocenter
City
Hammel
ZIP/Postal Code
8450
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
35906645
Citation
Naess-Schmidt ET, Thastum MM, Stabel HH, Odgaard L, Pedersen AR, Rask CU, Silverberg ND, Schroder A, Nielsen JF. Interdisciplinary intervention (GAIN) for adults with post-concussion symptoms: a study protocol for a stepped-wedge cluster randomised trial. Trials. 2022 Jul 29;23(1):613. doi: 10.1186/s13063-022-06572-7.
Results Reference
derived

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Get Going After concussioN 2.0

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