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My Healthy Brain: Preserving and Promoting Brain Health Through Evidence-based Practices

My Healthy Brain: Preserving and Promoting Brain Health Through Evidence-based Practices

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04537728
Enrollment
11
Registered
2020-09-03
Start date
2020-09-01
Completion date
2021-12-31
Last updated
2022-09-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aging, Cognitive Decline, Dementia, Mild Cognitive Impairment, Old Age; Dementia

Keywords

health, behavioral medicine, clinical psychology

Brief summary

The objective of this trial is to demonstrate early proof-of-concept for My Healthy Brain, an 8-week group program that directly targets multiple lifestyle factors associated with brain health and prevention of cognitive decline. The investigators will explore the feasibility, acceptability, and effect sizes of improvement in primary lifestyle outcomes as well as secondary outcomes of self-determination and subjective well-being.

Interventions

BEHAVIORALMy Healthy Brain Version 2

multimodal lifestyle intervention incorporating mindfulness skills, behavioral principles, and recent research on brain disease risk factors

Sponsors

Harvard Medical School (HMS and HSDM)
CollaboratorOTHER
Brigham and Women's Hospital
CollaboratorOTHER
Massachusetts General Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 60 years * English fluency/literacy * ≥1 modifiable brain disease risk factor (outlined by JAMA) * Bluetooth 4.0 enabled smartphone

Exclusion criteria

* Diagnosis of dementia; Montreal Cognitive Assessment \< 18 * Serious medical illness expected to worsen in next 6 months * Current suicidal ideation * Substance abuse * Untreated serious mental health conditions * Current use of digital monitoring device (eg. Fitbit) * Mindfulness practice (\> 45 minutes/week) in the last three months

Design outcomes

Primary

MeasureTime frameDescription
Credibility and Expectancy Questionnaire (CEQ)Baseline (0 Weeks)percent of participants that score beyond scale midpoint
Client Satisfaction Questionnaire (CSQ-3)Baseline (0 Weeks), Post-Test (8 Weeks)Items are summed to generate a total score; scores range from 3 to 12, with higher values indicating higher satisfaction.
Recruitment FeasibilityBaseline (0 Weeks)percent of referred patients meeting criteria to participate
Program AcceptabilityBaseline (0 Weeks), Post-Test (8 Weeks)percent of participants completing at least 6 sessions
Treatment FidelityBaseline (0 Weeks), Post-Test (8 Weeks)percent of sessions rated as 100% adherent
Assessment FeasibilityBaseline (0 Weeks), Post-Test (8 Weeks)percent of post-questionnaires completed
Adherence to ActigraphBaseline (0 Weeks), Post-Test (8 Weeks)percent of participants wearing Actiwatch ≥ 5 days per week
Adherence to Lifestyle BehaviorsBaseline (0 Weeks), Post-Test (8 Weeks)percent of participants completing weekly homework

Secondary

MeasureTime frameDescription
Physical Activity: Godin Leisure Time Exercise QuestionnaireBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; scores range from 0 to no upper limit, with higher scores indicating greater activity level.
Physical Activity: Rapid Assessment of Physical ActivityBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; the highest score with an affirmative response is used for scoring, with higher scores indicating greater physical activity.
Physical Activity: Actigraph measures of activityBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test
Nutrition: Mediterranean Eating Pattern for Americans ScreenerBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; scores range from 0-16, with higher scores indicating a greater adherence to the Mediterranean diet.
Nutrition: MIND Diet Adherence ChecklistBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; scores range greater than or equal to 0, with higher scores indicating creater adherence to MIND diet.
Medication and Substance Use: Morisky Medication Adherence ScaleBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; scores range from 0-4 with higher scores indicating greater adherence to medication regiment.
Medication and Substance Use: Alcohol Use Disorders Identification Test-ConsumptionBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; Scores range from 0-12, with higher scores indicating more hazardous drinking.
Medication and Substance Use: Fagerstrom Test for Nicotine DepedenceBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; scores range from 0-10, with higher total scores indicating greater physical dependence on nicotine.
Stress and Emotional Functioning: Perceived Stress ScaleBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; scores range from 0-40, with higher scores indicating greater perceived stress.
Change in Healthy AgingBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; measured by Brain Health Behaviors Checklist
Stress and Emotional Functioning: PROMIS AnxietyBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; scores range from 8-40, with higher scores indicating greater anxiety.
Stress and Emotional Functioning: Heart Rate Variability (Actigraphy)Baseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test
Social Functioning: PROMIS Social IsolationBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; scores range from 6-30, with higher scores indicating greater social isolation.
Social Functioning: PROMIS Emotional SupportBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; scores range from 4-16, with higher scores indicating lower emotional support.
Social Functioning: UCLA Loneliness ScaleBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; scores range from 0-24, with higher scores indicating stronger perceptions of loneliness and social isolation.
Cognitive Functioning: Everyday Cognition ScaleBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; scores range from 12-60, with higher scores indicating worse cognitive ability to perform everyday tasks.
Cognitive Functioning: PROMIS CognitionBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; scores range from 8-40, with higher scores indicating greater patient-perceived cognitive deficits.
Cognitive Functioning: Montreal Cognitive AssessmentBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; scores range from 0-30, with higher scores representing greater global cognitive capacity.
Stress and Emotional Functioning: PROMIS DepressionBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; scores range from 8-40, with higher scores indicating greater depression.
Mindfulness: Cognitive and Affective Mindfulness ScaleBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; Scores range from 12-48, with higher values reflecting greater mindfulness qualities.
Mindfulness: Homework logBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; measured by self-reported number of minutes practiced
Mindfulness: Five-Facet Mindfulness QuestionnaireBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; Scores range from 15-75, with higher scores indicating greater mindfulness.
Sleep: Pittsburgh Sleep Quality IndexBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test;Total scores range from 0 to 21, with higher scores indicating greater sleep disturbance.
Sleep: Jenkins Sleep QuestionnaireBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; scores range from 0-20, with higher scores indicating greater sleep disruption.
Sleep: Actigraph measures of sleepBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test
Physical Activity: PROMIS Physical FunctionBaseline (0 Weeks), Post-Test (8 Weeks)change from baseline to post test; scores range from 4-16, with higher scores signifying greater physical function.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026