N/A
N=40
Preventing Cognitive Decline
Cognitive Decline
Bottom Line
View on ClinicalTrials.gov: NCT05446909 ↗Enrolled (actual)
40
Serious AEs
0.0%
Results posted
Oct 2024
Primary outcome: Primary: Percentage of Trials Correct On Working Memory Test — 87.69; 91.57; 88.01; 91.68 percentage of correct trials — p=>0.05
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- IBMT mindfulness (Behavioral); health education (Behavioral)
- Age
- Adult, Older Adult · 40+ yrs
- Sex
- All
- Sponsor
- Arizona State University
- Primary completion
- Feb 2023
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percentage of Trials Correct On Working Memory Test |
87.69; 91.57; 88.01; 91.68 | >0.05 |
| PRIMARY Intervention Effects on Cognitive Decline |
5.34; 4.96; 5.29; 4.87 | >0.05 |
| PRIMARY Intervention Effects on Emotion Regulation |
5.71; 5.23; 5.50; 4.94 | >0.05 |
| PRIMARY Intervention Effects on Mindfulness |
2.92; 2.87; 3.92; 3.39 | <0.05 sig |
| SECONDARY Intervention Effects on Brain Function |
0.47; 0.51; 0.53; 0.49 | 0.754 |
| SECONDARY Intervention Effects on Brain White Matter |
0.42; 0.39; 0.43; 0.37 | 0.985 |
| SECONDARY Intervention Effects on Brain Grey Matter |
589.23; 569.39; 570.42; 576.87 | 0.877 |
Summary
The study aims to understand the mechanisms and training effects of evidence-based body-mind training on improving cognitive performance and preventing cognitive decline.
Eligibility Criteria
Inclusion Criteria
- Able to read/understand English
- Normal performance using standardized cognitive tests
- Self-reported decline in cognitive capacity such as memory loss
- Eligible for non-invasive fMRI
- Willing to be randomized
- Free of any severe psychiatric diagnoses or medication that may affect participation
Exclusion Criteria
- Medical disorders or medications that affect the central and autonomic nervous system; or a positive pregnancy test result (females)
- Unable to provide consent or understand study procedures due to mental illness or cognitive limitations
- Previous meditation experiences
- Evidence of illicit drug use
- Participants for blood draws weigh less than 110 lbs
- Metal or metallic materials in the body such as pacemaker
Data sourced from ClinicalTrials.gov (NCT05446909). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.