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Neurofeedback to Improve Working Memory in Mild Cognitive Impairment

Primary Purpose

Mild Cognitive Impairment

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Neurofeedback
Placebo
Sponsored by
University of California, San Diego
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mild Cognitive Impairment focused on measuring neurofeedback

Eligibility Criteria

50 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Meet criteria for mild cognitive impairment (MCI).
  2. Living independently.
  3. Literate in English.
  4. Competent to participate in the informed consent process and provide voluntary informed consent.

Exclusion Criteria:

  1. Frontal temporal dementia
  2. Active alcohol or substance use disorder within the past year.
  3. Brain cancer
  4. Stroke within the last 2 years
  5. Anti-epileptic medication
  6. Prior head injury involving loss of consciousness
  7. Seizure disorder
  8. Use of medications likely to affect cognitive function (cf. donepezil, memantine). We will not exclude for other medications but will examine their effects and include medications as covariates as appropriate (e.g., presence v. absence; anticholinergic load).
  9. The potential benefits of the study do not outweigh the potential risks of the study, as determined by the PI.

Sites / Locations

  • University of California at San DiegoRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Active Treatment

Placebo

Arm Description

Subjects will be given a choice of videos consisting of still images set to music. Whether the video progresses and music continues to play will depend on the subject's ability to maintain frontal gamma oscillatory activity within a prespecified range. Over successive weeks, the parameters for positive feedback (music and video progression) will become incrementally more difficult.

Video and music progression will be random and will not depend on brain activity. Any progression will be by random chance alone.

Outcomes

Primary Outcome Measures

Change in Working Memory accuracy
Change in the computerized test, N-back will be used to measure working memory.

Secondary Outcome Measures

Durability of Change in Working Memory accuracy
Change in the computerized test, N-back will be used to measure working memory.
Change in Gamma Band Response
Change in Gamma oscillations will be measured while the subject performs the n-back task.
Durability of Gamma Band Response
Change in Gamma oscillations will be measured while the subject performs the n-back task.

Full Information

First Posted
September 17, 2020
Last Updated
September 21, 2023
Sponsor
University of California, San Diego
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1. Study Identification

Unique Protocol Identification Number
NCT04566900
Brief Title
Neurofeedback to Improve Working Memory in Mild Cognitive Impairment
Official Title
Enhancing Gamma Band Response in Mild Cognitive Impairment to Improve Working Memory
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2021 (Actual)
Primary Completion Date
December 30, 2025 (Anticipated)
Study Completion Date
March 31, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, San Diego

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
Mild cognitive impairment (MCI) has been identified as an early phase of Alzheimer's disease (AD), a neurodegenerative disorder expected to affect 13.9 million Americans by 2060. AD causes a progressive cognitive decline, including problems related to learning and memory, that adversely affects life quality. Treatment intervention at the MCI stage of the disease could potentially slow down the rate at which people may convert from MCI to AD. Increasing evidence suggests that abnormal activity in frontal regions of the brain is associated with cognitive deficits observed in AD. Furthermore, previous research has shown that neurofeedback (NFB) training targeting these regions can improve memory, making it a potential treatment for AD. NFB is a technique where an individual learns to change his/her brain function in a particular direction, once that function has been made accessible through a visual or auditory metaphor. We are proposing a novel, computer-based brain-training program to enhance frontal gamma oscillatory activity in individuals with MCI. Results from this study will build the scientific foundation necessary for larger clinical trials dedicated to improving treatment options and outcomes for patients with MCI.
Detailed Description
This is a randomized, double-blind, clinical trial to test the efficacy of gamma-neurofeedback (G-NFB) compared to a placebo (P-NFB) in individuals with MCI. 112 consented participants will be randomized to receive G-NFB (n=56) or placebo-NFB (n=56) during 30-45 minute sessions twice per week for 12 weeks (24 total sessions). Memory and other cognitive domains will be measured using paper and pencil and computerized tests every 4 weeks during the study and at 4 weeks post completion of study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mild Cognitive Impairment
Keywords
neurofeedback

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
MCI subjects will be assigned to active intervention or placebo.
Masking
ParticipantCare ProviderOutcomes Assessor
Masking Description
Double-blind, randomized.
Allocation
Randomized
Enrollment
112 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Active Treatment
Arm Type
Experimental
Arm Description
Subjects will be given a choice of videos consisting of still images set to music. Whether the video progresses and music continues to play will depend on the subject's ability to maintain frontal gamma oscillatory activity within a prespecified range. Over successive weeks, the parameters for positive feedback (music and video progression) will become incrementally more difficult.
Arm Title
Placebo
Arm Type
Sham Comparator
Arm Description
Video and music progression will be random and will not depend on brain activity. Any progression will be by random chance alone.
Intervention Type
Behavioral
Intervention Name(s)
Neurofeedback
Intervention Description
Neurofeedback is a technique where brain functions are made accessible to the subject in the form of a metaphor. For instance, frontal brain activity may be shown as an airplane flying. Once the activity is made accessible, the subject can modulate it in a pre-specified direction. The parameters used to achieve successful feedback are made difficult over time and hence the brain is taught or conditioned to improve performance.
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Subjects in this arm will undergo all of the same testing as active treatment. Music and video progression will not depend on brain activity. Instead feedback will be random.
Primary Outcome Measure Information:
Title
Change in Working Memory accuracy
Description
Change in the computerized test, N-back will be used to measure working memory.
Time Frame
From baseline to 12 weeks of treatment
Secondary Outcome Measure Information:
Title
Durability of Change in Working Memory accuracy
Description
Change in the computerized test, N-back will be used to measure working memory.
Time Frame
From baseline to 4weeks post end of study
Title
Change in Gamma Band Response
Description
Change in Gamma oscillations will be measured while the subject performs the n-back task.
Time Frame
From baseline to 12 weeks of treatment
Title
Durability of Gamma Band Response
Description
Change in Gamma oscillations will be measured while the subject performs the n-back task.
Time Frame
From baseline to 4weeks post end of study

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Meet criteria for mild cognitive impairment (MCI). Living independently. Literate in English. Competent to participate in the informed consent process and provide voluntary informed consent. Exclusion Criteria: Frontal temporal dementia Active alcohol or substance use disorder within the past year. Brain cancer Stroke within the last 2 years Anti-epileptic medication Prior head injury involving loss of consciousness Seizure disorder Use of medications likely to affect cognitive function (cf. donepezil, memantine). We will not exclude for other medications but will examine their effects and include medications as covariates as appropriate (e.g., presence v. absence; anticholinergic load). The potential benefits of the study do not outweigh the potential risks of the study, as determined by the PI.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Joshua Phillips, B.S.
Phone
858-267-2257
Email
j7phillips@health.ucsd.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Fiza Singh, M.D.
Email
fsingh@health.ucsd.edu
Facility Information:
Facility Name
University of California at San Diego
City
La Jolla
State/Province
California
ZIP/Postal Code
92093
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fiza Singh, MD
Phone
858-922-4365
Email
fsingh@ucsd.edu

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
23020641
Citation
Diamond A. Executive functions. Annu Rev Psychol. 2013;64:135-68. doi: 10.1146/annurev-psych-113011-143750. Epub 2012 Sep 27.
Results Reference
background
PubMed Identifier
17915264
Citation
Dohnel K, Sommer M, Ibach B, Rothmayr C, Meinhardt J, Hajak G. Neural correlates of emotional working memory in patients with mild cognitive impairment. Neuropsychologia. 2008 Jan 15;46(1):37-48. doi: 10.1016/j.neuropsychologia.2007.08.012. Epub 2007 Aug 23.
Results Reference
background
PubMed Identifier
1422803
Citation
Leuchter AF, Newton TF, Cook IA, Walter DO, Rosenberg-Thompson S, Lachenbruch PA. Changes in brain functional connectivity in Alzheimer-type and multi-infarct dementia. Brain. 1992 Oct;115 ( Pt 5):1543-61. doi: 10.1093/brain/115.5.1543.
Results Reference
background
PubMed Identifier
17015233
Citation
Uhlhaas PJ, Singer W. Neural synchrony in brain disorders: relevance for cognitive dysfunctions and pathophysiology. Neuron. 2006 Oct 5;52(1):155-68. doi: 10.1016/j.neuron.2006.09.020.
Results Reference
background
PubMed Identifier
12488788
Citation
Stam CJ, van Cappellen van Walsum AM, Pijnenburg YA, Berendse HW, de Munck JC, Scheltens P, van Dijk BW. Generalized synchronization of MEG recordings in Alzheimer's Disease: evidence for involvement of the gamma band. J Clin Neurophysiol. 2002 Dec;19(6):562-74. doi: 10.1097/00004691-200212000-00010.
Results Reference
background

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Neurofeedback to Improve Working Memory in Mild Cognitive Impairment

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