RECRUITING

Internet-based Mind-Body Training for Brain Health

Description

The goal of this study is to conduct a Stage I pilot study examining the feasibility, acceptability, and preliminary effects of an internet-based, asynchronous mindfulness-based stress reduction program (iMBSR) compared to an internet-based, asynchronous lifestyle education program (iLifeEd), for adults at-risk for Alzheimer's disease (AD). Sixty middle-aged and older adults (aged 50 years or older) with subjective cognitive decline will be randomized to either an 8-week iMBSR program or an 8-week iLifeEd program control group, designed to provide adequate control for placebo effects. Behavioral, neuroimaging, and ecological momentary assessment (EMA) measures of mind-wandering will be administered to determine preliminary effects as a function of engagement in the iMBSR program. AD biomarkers will be examined at pre-training and post-training assessments.

Study Overview

Study Details

Study overview

The goal of this study is to conduct a Stage I pilot study examining the feasibility, acceptability, and preliminary effects of an internet-based, asynchronous mindfulness-based stress reduction program (iMBSR) compared to an internet-based, asynchronous lifestyle education program (iLifeEd), for adults at-risk for Alzheimer's disease (AD). Sixty middle-aged and older adults (aged 50 years or older) with subjective cognitive decline will be randomized to either an 8-week iMBSR program or an 8-week iLifeEd program control group, designed to provide adequate control for placebo effects. Behavioral, neuroimaging, and ecological momentary assessment (EMA) measures of mind-wandering will be administered to determine preliminary effects as a function of engagement in the iMBSR program. AD biomarkers will be examined at pre-training and post-training assessments.

Internet-based Mind-Body Training (iMBT) for Brain Health

Internet-based Mind-Body Training for Brain Health

Condition
Subjective Cognitive Decline
Intervention / Treatment

-

Contacts and Locations

Columbus

Department of Psychology, Columbus, Ohio, United States, 43201

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Aged 50 years or greater
  • * Capable of attending screening and assessment sessions and the internet-based intervention modules
  • * Fluent English speaker
  • * Corrected (near and far) visual acuity of 20/40 or better
  • * Adequate hearing for experimental purposes
  • * Absence of diagnosed terminal illness
  • * Absence of diagnosed neurological disorders
  • * No history of psychotic disorder or substance abuse disorder diagnosed by a psychologist or psychiatrist
  • * Absence of medication use that significantly alters brain activity
  • * No history of diagnosed learning disability that would interfere with the completion of the cognitive tasks
  • * Report elevated scores on the self-report Everyday Cognition (E-Cog)-39 subjective cognitive decline with normatively intact performance on cognitive testing (as determined by the neuropsychological battery)
  • * No evidence of mild cognitive impairment or dementia as assessed by the neuropsychological measures from the National Alzheimer's Coordinating Center (NACC) Uniform Data Set OR inadequate self-reported performance of instrumental activities of daily living
  • * Ability to engage in light stretching/movement-based activities with or without assistive devices
  • * Absence of any MRI contraindications
  • * Not pregnant and not attempting to become pregnant
  • * Absence of self-reported claustrophobia
  • * No regular practice of meditation or yoga (defined as once or more per week) AND No previous participation in a structured mindfulness class (e.g., Mindfulness-Based Stress Reduction, intensive meditation retreat)
  • * Access to internet and at-home computer with a working microphone and video
  • * Not enrolled in other RCTs examining the efficacy of exercise training, cognitive rehabilitation, stress management, progressive muscle relaxation or other health-based rehabilitation
  • * Aged less than 50 years
  • * Any physical or pragmatic limitation that prohibits attendance of screening or assessment sessions, or intervention engagement
  • * No fluency in English
  • * Corrected (near or far) visual acuity worse than 20/40
  • * Self-reported hearing impairment that would affect ability to hear the experimenter
  • * Diagnosis of terminal illness
  • * Presence of diagnosed neurological disorders such as: Alzheimer's disease, Vascular Dementia, Parkinson's disease, Multiple Sclerosis, Traumatic Brain Injury, Fronto-Temporal Lobar Degeneration, Lewy Body Disease
  • * History of psychotic disorder or substance abuse disorder diagnosed by a psychologist or psychiatrist
  • * Medication use that significantly alters brain activity
  • * History of diagnosed learning disability that would interfere with the completion of the cognitive tasks
  • * Does not report subjective cognitive decline AND/ OR does not perform in the normatively intact range on neuropsychological testing
  • * Evidence of mild cognitive impairment (MCI) or dementia OR inadequate self-reported performance of instrumental activities of daily living
  • * Any physical limitation or pragmatic limitation that prohibits attendance at assessment sessions and intervention modules with or without assistive devices
  • * Presence of MRI contraindications as assessed through the MRI screening form.
  • * Pregnant or attempting to become pregnant
  • * Self-reported claustrophobia
  • * Any regular practice of meditation or yoga (defined as once or more per week) OR Previous participation in a structured mindfulness class (e.g., Mindfulness-Based Stress Reduction, intensive meditation retreat)
  • * No access to internet or at-home computer with a working microphone and video
  • * Current enrollment in other RCTs examining the efficacy of exercise training, cognitive rehabilitation, stress management, progressive muscle relaxation or other health-based rehabilitation

Ages Eligible for Study

50 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Ohio State University,

Ruchika S Prakash, PhD, PRINCIPAL_INVESTIGATOR, Ohio State University

Study Record Dates

2026-03