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Cognitive Flexibility Training for Persistent Pain: Neuroimaging Pilot (COFLEX-i) (COFLEX-i)

Primary Purpose

Chronic Pain, Knee Pain Chronic, Hip Pain Chronic

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cognitive Training + fMRI
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Chronic Pain

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Adults between 18 to 70 years old with chronic hip, knee or back pain for >3 months
  • Documented moderate to severe chronic pain
  • English fluency
  • Access to a computer at home and an email account

Exclusion Criteria:

  • Lack of email/lack of basic computer skills
  • Diagnosed Alzheimer's or documented severe cognitive impairment
  • Severely impaired vision or color blindness
  • Unable to complete cognitive testing
  • An interventional pain procedure within one week prior to enrollment testing
  • Scheduled to undergo a pain procedure during the five weeks of cognitive training
  • Self-reported claustrophobia
  • Contraindication to an MRI scan (i.e. presence of metallic foreign body such as an artificial joint or aneurism clip, implanted pacemaker or spinal cord stimulator)

Sites / Locations

  • Washington University in Saint Louis

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Cognitive Training + fMRI

Arm Description

Participants will complete Trail Making Test (TMT) A & B (both electronic and paper-pencil), the paper-pencil Color-Word Matching Stroop Test (CWMST), and its electronic version called "Color Match", and a computer-based subset of NCPT (Neurocognitive Performance Test). In addition, participants will also complete Brief Pain Inventory (BPI), Hospital Anxiety and Depression Scale (HADS), Pain Catastrophizing Scale (PCS), and the Resilience Scale questionnaires at baseline. Participants will be provided with the cognitive training module and participants will be required to complete a targeted 36-minute daily training for 35 days. Participants will be asked to undergo 2 functional magnetic resonance imaging (fMRI) sessions. One prior to, and one after the 5-week cognitive training period.

Outcomes

Primary Outcome Measures

Changes in resting-state fMRI BOLD signal before and after 5 week cognitive training
Changes in resting-state fMRI BOLD (blood oxygenation level dependent) signal before and after 5-week cognitive training, within the default mode, frontoparietal, and cingulo-opercular brain networks.

Secondary Outcome Measures

Association between change in resting-state fMRI BOLD signal and the change in NCPT following cognitive training.
Association between change in resting state fMRI BOLD signal and the change in neurocognitive performance test (NCPT) score following 5 weeks of cognitive training.

Full Information

First Posted
October 10, 2018
Last Updated
April 12, 2022
Sponsor
Washington University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT03720821
Brief Title
Cognitive Flexibility Training for Persistent Pain: Neuroimaging Pilot (COFLEX-i)
Acronym
COFLEX-i
Official Title
Cognitive Flexibility Training for Persistent Pain: Neuroimaging Pilot (COFLEX-i)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
July 16, 2019 (Actual)
Primary Completion Date
June 30, 2021 (Actual)
Study Completion Date
February 25, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Washington University School of Medicine

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
To determine whether a 5-week computer-based cognitive training intervention results in changes in resting-state functional connectivity (rsFC) within the brain networks.
Detailed Description
This project is a single-center prospective pilot study to assess whether cognitive flexibility training through a Lumosity®-based training module over the course a five week timeframe in patients with chronic hip, knee, and back pain results in detectable changes in resting-state functional connectivity (rsFC). The investigators will explore changes in rsFC particularly within the default mode (DMN), frontoparietal (FPN), and cingulo-opercular (CON) brain networks.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Pain, Knee Pain Chronic, Hip Pain Chronic, Back Pain

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
46 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cognitive Training + fMRI
Arm Type
Experimental
Arm Description
Participants will complete Trail Making Test (TMT) A & B (both electronic and paper-pencil), the paper-pencil Color-Word Matching Stroop Test (CWMST), and its electronic version called "Color Match", and a computer-based subset of NCPT (Neurocognitive Performance Test). In addition, participants will also complete Brief Pain Inventory (BPI), Hospital Anxiety and Depression Scale (HADS), Pain Catastrophizing Scale (PCS), and the Resilience Scale questionnaires at baseline. Participants will be provided with the cognitive training module and participants will be required to complete a targeted 36-minute daily training for 35 days. Participants will be asked to undergo 2 functional magnetic resonance imaging (fMRI) sessions. One prior to, and one after the 5-week cognitive training period.
Intervention Type
Behavioral
Intervention Name(s)
Cognitive Training + fMRI
Intervention Description
Consented subjects will be asked to participate in the study for up to five months. Patients will be consented at the Washington University Department of Anesthesiology and will be asked to complete baseline resilience, pain, and anxiety and depression questionnaires, along with cognitive tests by pencil and paper that will be administered by a member of the research team. The participants will also be required to complete a computer-based Trails-making test, Color Match test, and NCPT (Neurocognitive Performance Test) battery at baseline, and undergo a functional magnetic resonance imaging (fMRI) session. All subjects will be asked to complete the three paper-pencil and computer-based measurements along with repeat pain questionnaire again 1-3 days after completion of training, undergo a second fMRI scan at that time, and complete the questionnaires again 3 months after the completion of training.
Primary Outcome Measure Information:
Title
Changes in resting-state fMRI BOLD signal before and after 5 week cognitive training
Description
Changes in resting-state fMRI BOLD (blood oxygenation level dependent) signal before and after 5-week cognitive training, within the default mode, frontoparietal, and cingulo-opercular brain networks.
Time Frame
5 weeks
Secondary Outcome Measure Information:
Title
Association between change in resting-state fMRI BOLD signal and the change in NCPT following cognitive training.
Description
Association between change in resting state fMRI BOLD signal and the change in neurocognitive performance test (NCPT) score following 5 weeks of cognitive training.
Time Frame
5 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Adults between 18 to 70 years old with chronic hip, knee or back pain for >3 months Documented moderate to severe chronic pain English fluency Access to a computer at home and an email account Exclusion Criteria: Lack of email/lack of basic computer skills Diagnosed Alzheimer's or documented severe cognitive impairment Severely impaired vision or color blindness Unable to complete cognitive testing An interventional pain procedure within one week prior to enrollment testing Scheduled to undergo a pain procedure during the five weeks of cognitive training Self-reported claustrophobia Contraindication to an MRI scan (i.e. presence of metallic foreign body such as an artificial joint or aneurism clip, implanted pacemaker or spinal cord stimulator)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Simon Haroutounian, PhD
Organizational Affiliation
Washington University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Washington University in Saint Louis
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
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Cognitive Flexibility Training for Persistent Pain: Neuroimaging Pilot (COFLEX-i)

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