Feasibility Testing of Cognitive Strategy Training in Post-Concussive Syndrome
Primary Purpose
Brain Concussion, Post-Concussion Syndrome
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
CO-OP Group
Sponsored by
About this trial
This is an interventional treatment trial for Brain Concussion focused on measuring metacognition, occupational therapy
Eligibility Criteria
Inclusion Criteria:
- Participants will be included if have a physician diagnosis of mTBI or if they meet the following criteria for mild traumatic brain injury established by the American Congress of rehabilitation Medicine including a traumatically induced physiological disruption of brain function, as manifested by at least one of the following: any loss of consciousness, any loss of memory for events immediately before or after the accident, any alteration in mental state at the time of the accident (e.g., feeling dazed, disoriented, or confused), and focal neurologic deficit(s) that may or may not be transient; severity of injury should not exceed a loss of consciousness >30 minutes, at 30 minutes post-injury a Glasgow Coma Scale score more severe than 13-15, or post-traumatic amnesia >24 hours.
- One or more post-concussive symptoms persisting for greater than 4 weeks that is inhibiting performance of one or more daily activities
- Age 18-60 years
Exclusion Criteria:
- Any additional severe neurologic or psychiatric conditions
- severe depressive symptoms per a score of >21 on the Patient Health Questionnaire (PHQ-9)
- inability to read, write, and speak English fluently
- lack of transportation to intervention sessions
Sites / Locations
- University of Missouri-Columbia
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
CO-OP Group
Arm Description
10, 45-60 minute Cognitive Orientation to daily Occupational Performance intervention sessions
Outcomes
Primary Outcome Measures
Client Satisfaction Questionnaire-8
Self-report, 8 item measures of intervention acceptability
recruitment rate
number enrolled/numberscreened AND Total # enrolled
retention rate
number completing study procedures/number enrolled
adherence rate
number of sessions attended/Total number of sessions
assessment battery feasibility
Time for completion
assessment battery feasibility
Percentage of assessment items complete
Secondary Outcome Measures
Canadian Occupation Performance Measure (COPM)
Self-report measures of perceived performance and satisfaction of occupational performance on a 1 to 10 Likert scale.
Neurobehavioral Symptom Inventory
Self-report measure on the severity and impact of common concussive symptoms using a 0 (none) to 4 (very severe) Likert scale.
Pittsburgh Sleep Quality Index
Self-report measure of quality and patterns of sleep using a four point Likert scale
Henry Ford Hospital Headache Disability Inventory
Self-report questionnaire of functional impact of headache symptoms
College of Optometrists in Vision Quality of Life Outcomes Assessment (COVD-QOL)
Self-report measure of functional impact of visual impairments using a five point Likert scale
Dysexecutive Questionnaire
Self-report measure functional impact of dysexecutive symptoms using five point Likert scale.
NIH Toolbox Cognition Battery
Neuropsychological, computer based tests of attention, executive functioning, episodic memory, working memory, language, and processing speed resulting in normative T-scores (mean=50; SD=10)
Weekly Calendar Planning Assessment
Performance-based measure of executive functioning within a calendar planning activity using accuracy and time to completion scores. Alternate forms available.
Full Information
NCT ID
NCT04681742
First Posted
December 16, 2020
Last Updated
March 8, 2023
Sponsor
University of Missouri-Columbia
1. Study Identification
Unique Protocol Identification Number
NCT04681742
Brief Title
Feasibility Testing of Cognitive Strategy Training in Post-Concussive Syndrome
Official Title
Feasibility Testing of Cognitive Strategy Training in Post-Concussive Syndrome
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
October 15, 2020 (Actual)
Primary Completion Date
December 31, 2022 (Actual)
Study Completion Date
December 31, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Missouri-Columbia
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 study will evaluate the practicality (i.e. acceptability to stakeholders; outcome battery feasibility; recruitment, retention, and adherence rates) and the preliminary effect of a cognitive strategy training intervention in adults with post-concussive syndrome.
Detailed Description
Up to 90% of known traumatic brain injuries are classified as mild, with many more injuries likely going undetected. While each of these individuals experiences somatic, cognitive, and/or affective symptoms acutely following the injury, an estimated 10-15% will continue to experience these symptoms for months up to a year post-injury. The persistence of symptoms for three months or greater is termed post-concussive syndrome (PCS) and can lead to decreases in academics, job performance, leisure, daily life activities, and routines. Traditionally, rehabilitation is either not provided to these individuals or has a specific focus on alleviating impairments (e.g. sustained attention) instead of mitigating effects on daily life function. Transfer of improvements in said impairments is known to be limited. Cognitive Orientation to daily Occupational Performance (CO-OP), a type of metacognitive strategy training, has known positive effects on activity performance outcomes in acquired brain injury (e.g. subacute and chronic stroke; moderate traumatic brain injury)1-5. CO-OP has yet to be evaluated in a sample of individuals with PCS. In sum, (1) CO-OP is an evidence-based intervention for improving activity performance, and (2) it is reasonable to hypothesize that the positive effects of CO-OP may be applied in PCS to overcome similar cognitive difficulties to improve activity performance.
The central research hypothesis is that a functionally-oriented metacognitive strategy training intervention, CO-OP, will be feasible and have a positive effect on activity performance in individuals with PCS syndrome. A single-group, prospective design with outcomes gathered pre-and post-intervention will be used (n=15) to evaluate the acceptability and feasibility of CO-OP in PCS. We will also be evaluating effect size on outcome measures of activity performance and perceptions of the functional impact of PCS symptoms.
Specific Aim 1: Determine the feasibility of CO-OP in Post-Concussive Syndrome. Hypothesis 1.1: Participants will report positive perceptions of the intervention via scores greater than 3 on the Client-Satisfaction Questionnaire. Hypothesis 1.2: The study will demonstrate acceptable recruitment, retention, and adherence rates. Hypothesis 1.3: The proposed assessment battery will be feasible (average completion time <2 hours).
Specific Aim 2: Explore the preliminary effect of CO-OP in a sample of individuals with PCS on activity performance outcomes. Hypothesis 2.1: The CO-OP group will demonstrate improvements in activity performance outcomes.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Concussion, Post-Concussion Syndrome
Keywords
metacognition, occupational therapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Actual)
8. Arms, Groups, and Interventions
Arm Title
CO-OP Group
Arm Type
Experimental
Arm Description
10, 45-60 minute Cognitive Orientation to daily Occupational Performance intervention sessions
Intervention Type
Behavioral
Intervention Name(s)
CO-OP Group
Intervention Description
CO-OP focuses on learning of a global problem-solving strategy, Goal-Plan-Do-Check (GPDC), within the performance of participant-chosen goals. Use of a broadly applicable strategy and meaningful activity ensures the intervention is salient to the participant and increases likelihood of transfer. Uniquely, therapists applying CO-OP use guided discovery methods, such as asking a series of probing questions, to support participants in analyzing their own performance of a given task and generating potential solutions for improving performance. Participants become equipped with these skills through repetitive application of the GPDC process. First, participants identify a specific goal (Goal). Then, participants consider a detailed plan (Plan) for accomplishing the goal. By carrying out the plan (Do) and critically analyzing the results (Check), participants determine how the plan worked. The intervention focuses on learning GPDC with gradual withdrawal of guided discovery methods.
Primary Outcome Measure Information:
Title
Client Satisfaction Questionnaire-8
Description
Self-report, 8 item measures of intervention acceptability
Time Frame
post-intervention only (10 weeks post-baseline)
Title
recruitment rate
Description
number enrolled/numberscreened AND Total # enrolled
Time Frame
calculated at end of intervention (10 weeks post-baseline)
Title
retention rate
Description
number completing study procedures/number enrolled
Time Frame
calculated at end of intervention (10 weeks post-baseline)
Title
adherence rate
Description
number of sessions attended/Total number of sessions
Time Frame
calculated at end of intervention (10 weeks post-baseline)
Title
assessment battery feasibility
Description
Time for completion
Time Frame
calculated at end of intervention (10 weeks post-baseline)
Title
assessment battery feasibility
Description
Percentage of assessment items complete
Time Frame
calculated at end of intervention (10 weeks post-baseline)
Secondary Outcome Measure Information:
Title
Canadian Occupation Performance Measure (COPM)
Description
Self-report measures of perceived performance and satisfaction of occupational performance on a 1 to 10 Likert scale.
Time Frame
Change from baseline to post-intervention (10 weeks)
Title
Neurobehavioral Symptom Inventory
Description
Self-report measure on the severity and impact of common concussive symptoms using a 0 (none) to 4 (very severe) Likert scale.
Time Frame
Change from baseline to post-intervention (10 weeks)
Title
Pittsburgh Sleep Quality Index
Description
Self-report measure of quality and patterns of sleep using a four point Likert scale
Time Frame
Change from baseline to post-intervention (10 weeks)
Title
Henry Ford Hospital Headache Disability Inventory
Description
Self-report questionnaire of functional impact of headache symptoms
Time Frame
Change from baseline to post-intervention (10 weeks)
Title
College of Optometrists in Vision Quality of Life Outcomes Assessment (COVD-QOL)
Description
Self-report measure of functional impact of visual impairments using a five point Likert scale
Time Frame
Change from baseline to post-intervention (10 weeks)
Title
Dysexecutive Questionnaire
Description
Self-report measure functional impact of dysexecutive symptoms using five point Likert scale.
Time Frame
Change from baseline to post-intervention (10 weeks)
Title
NIH Toolbox Cognition Battery
Description
Neuropsychological, computer based tests of attention, executive functioning, episodic memory, working memory, language, and processing speed resulting in normative T-scores (mean=50; SD=10)
Time Frame
Change from baseline to post-intervention (10 weeks)
Title
Weekly Calendar Planning Assessment
Description
Performance-based measure of executive functioning within a calendar planning activity using accuracy and time to completion scores. Alternate forms available.
Time Frame
Change from baseline to post-intervention (10 weeks)
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:
Participants will be included if have a physician diagnosis of mTBI or if they meet the following criteria for mild traumatic brain injury established by the American Congress of rehabilitation Medicine including a traumatically induced physiological disruption of brain function, as manifested by at least one of the following: any loss of consciousness, any loss of memory for events immediately before or after the accident, any alteration in mental state at the time of the accident (e.g., feeling dazed, disoriented, or confused), and focal neurologic deficit(s) that may or may not be transient; severity of injury should not exceed a loss of consciousness >30 minutes, at 30 minutes post-injury a Glasgow Coma Scale score more severe than 13-15, or post-traumatic amnesia >24 hours.
One or more post-concussive symptoms persisting for greater than 4 weeks that is inhibiting performance of one or more daily activities
Age 18-60 years
Exclusion Criteria:
Any additional severe neurologic or psychiatric conditions
severe depressive symptoms per a score of >21 on the Patient Health Questionnaire (PHQ-9)
inability to read, write, and speak English fluently
lack of transportation to intervention sessions
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anna Boone, PhD
Organizational Affiliation
University of Missouri-Columbia
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Missouri-Columbia
City
Columbia
State/Province
Missouri
ZIP/Postal Code
65212
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
21309372
Citation
Henshaw E, Polatajko H, McEwen S, Ryan JD, Baum CM. Cognitive approach to improving participation after stroke: two case studies. Am J Occup Ther. 2011 Jan-Feb;65(1):55-63. doi: 10.5014/ajot.2011.09010.
Results Reference
background
PubMed Identifier
23796683
Citation
Dawson DR, Binns MA, Hunt A, Lemsky C, Polatajko HJ. Occupation-based strategy training for adults with traumatic brain injury: a pilot study. Arch Phys Med Rehabil. 2013 Oct;94(10):1959-63. doi: 10.1016/j.apmr.2013.05.021. Epub 2013 Jun 22.
Results Reference
background
PubMed Identifier
19456090
Citation
Dawson DR, Gaya A, Hunt A, Levine B, Lemsky C, Polatajko HJ. Using the cognitive orientation to occupational performance (CO-OP) with adults with executive dysfunction following traumatic brain injury. Can J Occup Ther. 2009 Apr;76(2):115-27. doi: 10.1177/000841740907600209.
Results Reference
background
PubMed Identifier
25416738
Citation
McEwen S, Polatajko H, Baum C, Rios J, Cirone D, Doherty M, Wolf T. Combined Cognitive-Strategy and Task-Specific Training Improve Transfer to Untrained Activities in Subacute Stroke: An Exploratory Randomized Controlled Trial. Neurorehabil Neural Repair. 2015 Jul;29(6):526-36. doi: 10.1177/1545968314558602. Epub 2014 Nov 21.
Results Reference
background
PubMed Identifier
22389945
Citation
Polatajko HJ, McEwen SE, Ryan JD, Baum CM. Pilot randomized controlled trial investigating cognitive strategy use to improve goal performance after stroke. Am J Occup Ther. 2012 Jan-Feb;66(1):104-9. doi: 10.5014/ajot.2012.001784.
Results Reference
background
PubMed Identifier
28125305
Citation
Bergersen K, Halvorsen JO, Tryti EA, Taylor SI, Olsen A. A systematic literature review of psychotherapeutic treatment of prolonged symptoms after mild traumatic brain injury. Brain Inj. 2017;31(3):279-289. doi: 10.1080/02699052.2016.1255779. Epub 2017 Jan 26.
Results Reference
background
PubMed Identifier
17060147
Citation
Lundin A, de Boussard C, Edman G, Borg J. Symptoms and disability until 3 months after mild TBI. Brain Inj. 2006 Jul;20(8):799-806. doi: 10.1080/02699050600744327.
Results Reference
background
PubMed Identifier
22220505
Citation
Schmitter-Edgecombe M, Seelye AM. Recovery of content and temporal order memory for performed activities following moderate to severe traumatic brain injury. J Clin Exp Neuropsychol. 2012;34(3):256-68. doi: 10.1080/13803395.2011.633497. Epub 2012 Jan 6.
Results Reference
background
PubMed Identifier
23855364
Citation
McCrory P, Meeuwisse WH, Aubry M, Cantu RC, Dvorak J, Echemendia RJ, Engebretsen L, Johnston K, Kutcher JS, Raftery M, Sills A, Benson BW, Davis GA, Ellenbogen R, Guskiewicz KM, Herring SA, Iverson GL, Jordan BD, Kissick J, McCrea M, McIntosh AS, Maddocks D, Makdissi M, Purcell L, Putukian M, Schneider K, Tator CH, Turner M. Consensus statement on concussion in sport: the 4th International Conference on Concussion in Sport, Zurich, November 2012. J Athl Train. 2013 Jul-Aug;48(4):554-75. doi: 10.4085/1062-6050-48.4.05. No abstract available.
Results Reference
background
PubMed Identifier
28301451
Citation
Taylor CA, Bell JM, Breiding MJ, Xu L. Traumatic Brain Injury-Related Emergency Department Visits, Hospitalizations, and Deaths - United States, 2007 and 2013. MMWR Surveill Summ. 2017 Mar 17;66(9):1-16. doi: 10.15585/mmwr.ss6609a1.
Results Reference
background
PubMed Identifier
19285163
Citation
Jagoda AS, Bazarian JJ, Bruns JJ Jr, Cantrill SV, Gean AD, Howard PK, Ghajar J, Riggio S, Wright DW, Wears RL, Bakshy A, Burgess P, Wald MM, Whitson RR. Clinical policy: neuroimaging and decisionmaking in adult mild traumatic brain injury in the acute setting. J Emerg Nurs. 2009 Apr;35(2):e5-40. doi: 10.1016/j.jen.2008.12.010.
Results Reference
background
PubMed Identifier
23299259
Citation
King PR, Donnelly KT, Donnelly JP, Dunnam M, Warner G, Kittleson CJ, Bradshaw CB, Alt M, Meier ST. Psychometric study of the Neurobehavioral Symptom Inventory. J Rehabil Res Dev. 2012;49(6):879-88. doi: 10.1682/jrrd.2011.03.0051.
Results Reference
background
PubMed Identifier
9720850
Citation
Carpenter JS, Andrykowski MA. Psychometric evaluation of the Pittsburgh Sleep Quality Index. J Psychosom Res. 1998 Jul;45(1):5-13. doi: 10.1016/s0022-3999(97)00298-5.
Results Reference
background
PubMed Identifier
8190284
Citation
Jacobson GP, Ramadan NM, Aggarwal SK, Newman CW. The Henry Ford Hospital Headache Disability Inventory (HDI). Neurology. 1994 May;44(5):837-42. doi: 10.1212/wnl.44.5.837.
Results Reference
background
PubMed Identifier
29265865
Citation
Carlozzi NE, Tulsky DS, Wolf TJ, Goodnight S, Heaton RK, Casaletto KB, Wong AWK, Baum CM, Gershon RC, Heinemann AW. Construct validity of the NIH Toolbox Cognition Battery in individuals with stroke. Rehabil Psychol. 2017 Nov;62(4):443-454. doi: 10.1037/rep0000195.
Results Reference
background
PubMed Identifier
23106990
Citation
Weiner NW, Toglia J, Berg C. Weekly Calendar Planning Activity (WCPA): a performance-based assessment of executive function piloted with at-risk adolescents. Am J Occup Ther. 2012 Nov-Dec;66(6):699-708. doi: 10.5014/ajot.2012.004754.
Results Reference
background
PubMed Identifier
16209417
Citation
Bennett PC, Ong B, Ponsford J. Measuring executive dysfunction in an acute rehabilitation setting: using the dysexecutive questionnaire (DEX). J Int Neuropsychol Soc. 2005 Jul;11(4):376-85. doi: 10.1017/s1355617705050423.
Results Reference
background
PubMed Identifier
11556941
Citation
Kroenke K, Spitzer RL, Williams JB. The PHQ-9: validity of a brief depression severity measure. J Gen Intern Med. 2001 Sep;16(9):606-13. doi: 10.1046/j.1525-1497.2001.016009606.x.
Results Reference
background
PubMed Identifier
10259963
Citation
Attkisson CC, Zwick R. The client satisfaction questionnaire. Psychometric properties and correlations with service utilization and psychotherapy outcome. Eval Program Plann. 1982;5(3):233-7. doi: 10.1016/0149-7189(82)90074-x.
Results Reference
background
PubMed Identifier
19932442
Citation
Maples WC, Hoenes R. The College of Optometrists in Vision Development checklist related to vision function: expert opinions. Optometry. 2009 Dec;80(12):688-94. doi: 10.1016/j.optm.2009.06.003.
Results Reference
background
PubMed Identifier
10104738
Citation
Law M, Baptiste S, McColl M, Opzoomer A, Polatajko H, Pollock N. The Canadian occupational performance measure: an outcome measure for occupational therapy. Can J Occup Ther. 1990 Apr;57(2):82-7. doi: 10.1177/000841749005700207.
Results Reference
background
PubMed Identifier
31360793
Citation
Ferreira IS, Pinto CB, Saleh Velez FG, Leffa DT, Vulcano de Toledo Piza P, Fregni F. Recruitment challenges in stroke neurorecovery clinical trials. Contemp Clin Trials Commun. 2019 Jul 5;15:100404. doi: 10.1016/j.conctc.2019.100404. eCollection 2019 Sep. Erratum In: Contemp Clin Trials Commun. 2020 Dec 10;20:100689.
Results Reference
background
PubMed Identifier
18547501
Citation
French B, Leathley M, Sutton C, McAdam J, Thomas L, Forster A, Langhorne P, Price C, Walker A, Watkins C. A systematic review of repetitive functional task practice with modelling of resource use, costs and effectiveness. Health Technol Assess. 2008 Jul;12(30):iii, ix-x, 1-117. doi: 10.3310/hta12300.
Results Reference
background
PubMed Identifier
25363626
Citation
Waljas M, Iverson GL, Lange RT, Hakulinen U, Dastidar P, Huhtala H, Liimatainen S, Hartikainen K, Ohman J. A prospective biopsychosocial study of the persistent post-concussion symptoms following mild traumatic brain injury. J Neurotrauma. 2015 Apr 15;32(8):534-47. doi: 10.1089/neu.2014.3339. Epub 2015 Feb 25.
Results Reference
background
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Feasibility Testing of Cognitive Strategy Training in Post-Concussive Syndrome
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