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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
University of Missouri-Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Brain Concussion focused on measuring metacognition, occupational therapy

Eligibility Criteria

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

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

First Posted
December 16, 2020
Last Updated
March 8, 2023
Sponsor
University of Missouri-Columbia
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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

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Feasibility Testing of Cognitive Strategy Training in Post-Concussive Syndrome

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