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The Effect of Cognitive Rehabilitation Therapy in Improving Cognitive Function of Attention Following Mild Traumatic Brain Injury

Primary Purpose

Mild Traumatic Brain Injury, Cognitive Impairment

Status
Completed
Phase
Not Applicable
Locations
Malaysia
Study Type
Interventional
Intervention
Structured cognitive rehabilitation therapy
Patient-centred cognitive therapy
Sponsored by
University of Malaya
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mild Traumatic Brain Injury focused on measuring cognitive rehabilitation, diffusion tensor imaging, neuropsychology, functional outcome

Eligibility Criteria

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

Inclusion Criteria:

  • Mild traumatic brain injury as a result of motor vehicle accidents only.
  • No previous history of head trauma.
  • Education level of a minimum of 9 years (required for neuropsychological test).
  • Normal Computed Tomography (CT) brain scan finding.
  • Able to comply with cognitive rehabilitation therapy.
  • No pre-existing chronic illness that can cause neurological complications, neurological diseases or psychiatric condition.
  • Not on any regular medication that may alter or effect cognitive and psychological status.

Exclusion Criteria:

  • Normal neuropsychological assessment test result at 3 months post injury (planned test time) for both study groups.
  • Clinical evidence of alcohol influence at time of injury.
  • Non Malaysian citizens
  • Major polytrauma including long bone fractures, intra-abdominal injuries and chest injuries that require surgical and/or metal insertion.

Sites / Locations

  • University Malaya Medical Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Individualised structured cognitive rehabilitation therapy

Patient-centred cognitive therapy

Arm Description

Participants of interventional arm will receive individualised structured cognitive rehabilitation therapy at the proposed health centre (University Malaya Medical Centre, Malaysia).

Participants of conventional arm will receive an existing cognitive rehabilitation treatment available at the proposed health centre (University Malaya Medical Centre, Malaysia).

Outcomes

Primary Outcome Measures

Change in Neuropsychological Assessment Battery- Screening score
Measure the change in score of Attention domain screening score and Total Screening Index Score at two different time points - 3 months and 6 months post brain injury.

Secondary Outcome Measures

Change in Diffusion Tensor Imaging parameters
Measure the change in mean values of white matter tract parameters at two different time points - 3 months and 6 months post brain injury.
Change in Goal Attainment Scaling score
Measure the change in Goal Attainment Scaling calculation score at two different time points - 3 months and 6 months post brain injury.

Full Information

First Posted
July 18, 2017
Last Updated
November 5, 2020
Sponsor
University of Malaya
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1. Study Identification

Unique Protocol Identification Number
NCT03237676
Brief Title
The Effect of Cognitive Rehabilitation Therapy in Improving Cognitive Function of Attention Following Mild Traumatic Brain Injury
Official Title
The Effect of Cognitive Rehabilitation Therapy in Improving Cognitive Function of Attention Following Mild Traumatic Brain Injury
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Completed
Study Start Date
August 1, 2017 (Actual)
Primary Completion Date
April 30, 2019 (Actual)
Study Completion Date
December 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Malaya

4. Oversight

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

5. Study Description

Brief Summary
This research is a randomised controlled study. The study hypothesis is cognitive rehabilitation for attention deficits following mild traumatic brain injury will improve patient's cognitive outcome, measured by neuropsychological and neuroimaging parameters. Participant recruitment is from University Malaya Medical Centre, Malaysia. All mild traumatic brain injury participants have to fulfil the study inclusion criteria and written consented for therapy. Control group receives existing patient-centred cognitive treatment whereas intervention group receives individualised structured cognitive rehabilitation therapy. The intervention begins at three months post injury and ends at six months post injury. Study outcome measurements are applied at pre and post treatment. This study was ethically approved by Medical Research Ethics Committee University Malaya Medical Centre (MREC ID NO: 2016928-4293).
Detailed Description
General study objective: to measure the effect of cognitive rehabilitation program for attention deficit applied in mild traumatic brain injury patients. Specific objectives: To measure the effect of a 12-week cognitive rehabilitation therapy for attention deficits in mild traumatic brain injury patients using neuropsychological and functional assessments. To examine the correlation between neurocognitive deficits and structural brain changes at baseline and at six months post injury. Study type and location: An interventional study conducted in University Malaya Medical Centre (UMMC), Malaysia. Participants: Patients diagnosed with mild traumatic brain injury at Accident & Emergency Department in UMMC. Outcome measures: Neuropsychological Assessment Battery-Screening test Diffusion Tensor Imaging parameters Goal Attainment Scaling Ethics approval: approved MREC ID NO: 2016928-4293 Consent: informed written consent will be obtained from all participants of research. Estimated sample size: Based on medium effect size Cohen's d = 0.35 Investigators used G*Power Version 3.1.9.2 for sample size calculation. Sample size calculated: 60 Estimating drop out rate of 40%=24. Therefore sample size target n= 84 mTBI patients. Study design: A two arm randomised controlled trial: Mild traumatic brain injury control group, and Mild traumatic brain injury intervention group. The study protocol is divided into 3 segments: Neurocognitive evaluation protocol: Investigators will perform Neuropsychological Assessment Battery-Screening test on both groups at three months and at six months following brain injury. Imaging protocol: Investigators perform Diffusion Tensor Imaging for both groups at three months and at six months following brain injury. Cognitive rehabilitation therapy protocol: The focus is on attention deficits. Each study arm will receive different treatment approaches. Mild traumatic brain injury control group will receive a patient-centred cognitive therapy. This is an application of existing cognitive rehabilitation treatment available at UMMC, which include therapy session on symptoms management and coping strategies. This is performed and monitored by a cognitive therapy trained Occupational Therapist. Clinical and treatment review are provided as part of routine outpatient rehabilitation clinic review. Mild traumatic brain injury intervention group will receive individualised structured cognitive rehabilitation therapy that consist of: Direct attention training: A deficit-oriented evidence-based treatment approach. The therapy for attention is computer-based and is divided into focused attention, selective attention, divided attention and sustained attention. Each treatment session is conducted by a trained Occupational Therapist in cognitive therapy and a rehabilitation medicine physician. Strategic approach (metacognitive): This involves generalisation of tasks to everyday functional skills. This approach is applied after each direct attention training session. This approach include review of individualised goals, review of cognitive related problem(s) encountered in participants daily activities since injury and problem-solving training. This is also performed by similar trained Occupational Therapist and reviewed by a rehabilitation medicine physician. Randomisation sampling: Investigators apply simple randomisation in selection of mild traumatic brain injury control and intervention group participants.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mild Traumatic Brain Injury, Cognitive Impairment
Keywords
cognitive rehabilitation, diffusion tensor imaging, neuropsychology, functional outcome

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
intervention group receives structured cognitive rehabilitation therapy, control group receives conventional/pre-existing cognitive rehabilitation therapy.
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
Participants are randomised on treatment arm. Co-investigators are blinded from knowing which participant receives which treatment arm. Cognitive outcome assessor is blinded from knowing which participant receives which treatment arm.
Allocation
Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Individualised structured cognitive rehabilitation therapy
Arm Type
Experimental
Arm Description
Participants of interventional arm will receive individualised structured cognitive rehabilitation therapy at the proposed health centre (University Malaya Medical Centre, Malaysia).
Arm Title
Patient-centred cognitive therapy
Arm Type
Active Comparator
Arm Description
Participants of conventional arm will receive an existing cognitive rehabilitation treatment available at the proposed health centre (University Malaya Medical Centre, Malaysia).
Intervention Type
Other
Intervention Name(s)
Structured cognitive rehabilitation therapy
Other Intervention Name(s)
cognitive therapy, CogniPlus
Intervention Description
A computer-based cognitive rehabilitation therapy Therapy frequency is one hour session per week for three months.
Intervention Type
Other
Intervention Name(s)
Patient-centred cognitive therapy
Intervention Description
Application of existing cognitive therapy at University Malaya Medical Centre, Malaysia. It is a patient-centred therapy approach over a period of three months, which include therapy session on symptoms management and coping strategies. Clinical and treatment review are provided as part of routine outpatient rehabilitation clinic review.
Primary Outcome Measure Information:
Title
Change in Neuropsychological Assessment Battery- Screening score
Description
Measure the change in score of Attention domain screening score and Total Screening Index Score at two different time points - 3 months and 6 months post brain injury.
Time Frame
Perform at 3 months (pre-intervention) and 6 months (completed intervention) following mild traumatic brain injury
Secondary Outcome Measure Information:
Title
Change in Diffusion Tensor Imaging parameters
Description
Measure the change in mean values of white matter tract parameters at two different time points - 3 months and 6 months post brain injury.
Time Frame
Perform at 3 months (pre-intervention) and 6 months (completed intervention) following mild traumatic brain injury
Title
Change in Goal Attainment Scaling score
Description
Measure the change in Goal Attainment Scaling calculation score at two different time points - 3 months and 6 months post brain injury.
Time Frame
Perform at 3 months (baseline) and 6 months (complete intervention) following mild traumatic brain injury

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: Mild traumatic brain injury as a result of motor vehicle accidents only. No previous history of head trauma. Education level of a minimum of 9 years (required for neuropsychological test). Normal Computed Tomography (CT) brain scan finding. Able to comply with cognitive rehabilitation therapy. No pre-existing chronic illness that can cause neurological complications, neurological diseases or psychiatric condition. Not on any regular medication that may alter or effect cognitive and psychological status. Exclusion Criteria: Normal neuropsychological assessment test result at 3 months post injury (planned test time) for both study groups. Clinical evidence of alcohol influence at time of injury. Non Malaysian citizens Major polytrauma including long bone fractures, intra-abdominal injuries and chest injuries that require surgical and/or metal insertion.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Norhamizan Hamzah, MBChB,MRehabMed
Organizational Affiliation
Rehabilitation Medicine Specialist, University of Malaya
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mazlina Mazlan, MBBS,MRehabMed
Organizational Affiliation
Consultant Rehabilitation Medicine & Associate Professor, University of Malaya
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Vairavan Narayanan, MBBS,MSURG,FRCS
Organizational Affiliation
Consultant Neurosurgeon & Associate Professor, University of Malaya
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Norlisah Ramli, MBBS,FRCR
Organizational Affiliation
Consultant Neuroradiologist & Professor, University of Malaya
Official's Role
Study Chair
Facility Information:
Facility Name
University Malaya Medical Centre
City
Kuala Lumpur
State/Province
Wilayah Persekutuan
ZIP/Postal Code
59100
Country
Malaysia

12. IPD Sharing Statement

Citations:
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25952562
Citation
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Results Reference
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27751922
Citation
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Results Reference
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Citation
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Citation
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The Effect of Cognitive Rehabilitation Therapy in Improving Cognitive Function of Attention Following Mild Traumatic Brain Injury

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