Mindfulness and Attention Training Intervention to Lower Distractibility in Aging
NCT ID: NCT05974605
Last Updated: 2024-12-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
16 participants
INTERVENTIONAL
2022-03-17
2024-06-27
Brief Summary
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Detailed Description
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In this project, there is a single training arm that will train healthy older adults on a combination training composed of high attentional control and mindfulness meditation using simulation based games. Neural and cognitive changes in near and far transfer tasks will be examined immediately after the intervention. These changes will be compared with that of a previously collected group of older adults who received only cognitive control training (NCT03988829; Arms 1 and 2). Changes in overall cognition (primary cognitive outcome) and changes in DMN connectivity during task (primary neuroimaging outcome) and rest (secondary neuroimaging outcome) in this combination training group will be compared to the respective changes in Arm 1 (low attentional control training) and Arm 2 (High Attentional Control training) of the existing dataset. The protocol of participant recruitment, pre- and post- training assessments (MRI and behavioral), and training platform remain same between this study and the existing database. In this current study, participants also undergo a functional near infra-red spectroscopy (fNIRS) session, after completion of behavioral and MRI session, at pre-training and post-training. This clinical trial will result in the development of more efficient behavioral intervention tools in older adults, based on neuroimaging evidence, that can be readily used from the comfort of home.
Conditions
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Study Design
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NA
SINGLE_GROUP
PREVENTION
NONE
Study Groups
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Combined mindfulness meditation and cognitive training
Participants train at home for 20 hours over 8 weeks, splitting the time between mindfulness meditation and cognitive training. Participants train for 30 minutes per day, for 5 days a weeks on a provided tablet computer. The participants are to keep a paper log of dates and durations.
The mindfulness meditation portion of the training is a commercially available mobile app. Participants listen to guided meditations and follow the instructions. The program includes common mindfulness meditation exercises such as body scan or breath awareness.
The cognitive training portion of the intervention uses a highly demanding attentional control training program BirdWatch game (BWGU). BWGU is a "gamified" n-back paradigm where participants randomly switch the focus of attention to update or maintain an adaptively growing set of bird stimuli in their working memory and are sometimes required to inhibit their response.
MM+HighC
In this intervention, participants will be trained on a available mindfulness meditation app, followed by a working memory updating game, developed by Dr. Chandramallika Basak. This game requires high degree of attentional control (Unpredictable Bird Watch), also known as High-C. The app and the game are delivered through an Android tablet for this home-based training.
Interventions
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MM+HighC
In this intervention, participants will be trained on a available mindfulness meditation app, followed by a working memory updating game, developed by Dr. Chandramallika Basak. This game requires high degree of attentional control (Unpredictable Bird Watch), also known as High-C. The app and the game are delivered through an Android tablet for this home-based training.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* aged 65 to 85 years old
* at least high school education
* learned English before age 5.
* screening cognitive assessment (MoCA) score above the threshold
* physical and sensory capacity sufficient to undertake an fMRI study:
* the ability to stay still for the duration of the scan
* sufficient finger dexterity to press buttons on the provided button boxes during the scan
* vision acuity of at least 20/30 after correction
* no color blindness
* no claustrophobia
* no metal implants above the waist
* if female, cannot be pregnant or likely to be pregnant.
* cannot have participated in similar training in the past two years.
Exclusion Criteria
* weigh over 300 lb
* did not attain at least high school education
* have not learned English before the age of 5
* screening cognitive assessment (MoCA) score below the threshold
* color blind
* have vision acuity worse than 20/30 after correction
* experience of excessive hand tremor or other motor impairment related to hand movement
* history of cardiovascular disease other than treated hypertension
* diabetes
* psychiatric disorders
* illness or trauma affecting the central nervous system, including stroke and head trauma resulting in loss of consciousness over 5 seconds
* substance/alcohol abuse
* use of medication with anti-depressant, anti-psychotic effects (use of hypnotic medication is allowed only occasionally at bedtime).
* certain medical devices or implants
* non-medical sources of metal, e.g., shrapnel, prior hobby/work with metal
* MRI image revealing evidence of pathology
* female participants that are pregnant or likely to become pregnant
* participated in similar training in the past two years
65 Years
85 Years
ALL
Yes
Sponsors
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The University of Texas at Dallas
OTHER
Responsible Party
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Chandramallika Basak
Associate Professor
Principal Investigators
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Paulina Skolasinska, MS
Role: PRINCIPAL_INVESTIGATOR
The University of Texas at Dallas
Chandramallika Basak, PhD
Role: STUDY_DIRECTOR
The University of Texas at Dallas
Locations
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Center for Vital Longevity
Dallas, Texas, United States
Countries
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References
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Geda YE. Mild cognitive impairment in older adults. Curr Psychiatry Rep. 2012 Aug;14(4):320-7. doi: 10.1007/s11920-012-0291-x.
Basak C, Qin S, O'Connell MA. Differential effects of cognitive training modules in healthy aging and mild cognitive impairment: A comprehensive meta-analysis of randomized controlled trials. Psychol Aging. 2020 Mar;35(2):220-249. doi: 10.1037/pag0000442. Epub 2020 Feb 3.
Provided Documents
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Document Type: Informed Consent Form
Other Identifiers
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IRB-22-189
Identifier Type: -
Identifier Source: org_study_id