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Clinical Trials/NCT04798885
NCT04798885Active, not recruitingNot Applicable

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

University of Aarhus1 site in 1 country310 target enrollmentStarted: May 12, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
310
Locations
1
Primary Endpoint
Change of at least seven in the sum score on the Rivermead Post-Concussion Symptoms Questionnaire (RPQ)

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

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 ≥
  • •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.

Arms & Interventions

Enhanced usual care

No Intervention

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.

GAIN 2.0 intervention

Experimental

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

Intervention: GAIN 2.0 (Behavioral)

Outcomes

Primary Outcomes

Change of at least seven in the sum score on the Rivermead Post-Concussion Symptoms Questionnaire (RPQ)

Time Frame: Three months after end of treatment

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 Outcomes

  • Long term sick leave defined as public assistance benefits related to illness in more than three consecutive weeks(Within 12 months after concussion)
  • 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(Within 36 months after concussion)
  • Proportion of employed participants defined as receiving no public assistance benefits except from state education fund grants(At 36 months after concussion)
  • Sumscore in the dimension 'time spend on daily activities' on the Utrecht Scale for Evaluation of Rehabilitation-Participation (USER-P).(Three months after end of treatment)
  • Degree of job stability based on whether labor market contributions have been paid(At 36 months after concussion)
  • Sumscore in the dimension 'limitations' on the Utrecht Scale for Evaluation of Rehabilitation-Participation (USER-P)(Three months after end of treatment)
  • Sumscore in the dimension 'satisfaction with participation' on the Utrecht Scale for Evaluation of Rehabilitation-Participation (USER-P)(Three months after end of treatment)
  • Proportion of employed participants defined as receiving no public assistance benefits except from state education fund grants(At 12 months after concussion)
  • Degree of job stability based on whether labor market contributions have been paid(At 12 months after concussion)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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