NCT06210035

Brief Summary

In the current study, we will examine how two types of concentration meditation practices affect plasma biomarkers of Alzheimer's Disease (AD). We will also examine the effects of the two types of meditation practices on emotional well-being and episodic memory. Healthy adults aged 18-35 who meet all eligibility criteria will be invited to this study. Participants will be asked to engage in one week of daily meditation practice or no-intervention control task at home. They will also be asked to visit the lab twice, once before and once after the intervention, to provide blood samples to assess plasma biomarkers of AD and to complete emotion questionnaires and a memory test.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
94

participants targeted

Target at P50-P75 for not_applicable alzheimer-disease

Timeline
Completed

Started Jan 2024

Shorter than P25 for not_applicable alzheimer-disease

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 20, 2023

Completed
3 months until next milestone

First Posted

Study publicly available on registry

January 18, 2024

Completed
11 days until next milestone

Study Start

First participant enrolled

January 29, 2024

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 3, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 3, 2024

Completed
1.7 years until next milestone

Results Posted

Study results publicly available

January 5, 2026

Completed
Last Updated

January 5, 2026

Status Verified

December 1, 2025

Enrollment Period

3 months

First QC Date

October 20, 2023

Results QC Date

November 4, 2025

Last Update Submit

December 12, 2025

Conditions

Outcome Measures

Primary Outcomes (2)

  • Change in Plasma Amyloid Beta (Aβ) Levels

    The investigators computed an aggregate Z-score based on plasma Aβ40 and Aβ42 levels (pg/mL). A Z-score of 0 represents the sample mean. Higher values indicate a greater level of plasma Aβ, which in cognitively normal individuals has been found to be associated with a higher risk of converting to Alzheimer's disease (Song et al., 2011). They conducted a 2 (time: pre, post) × 3 (condition) ANOVA to test for a time × condition interaction in plasma Aβ levels, assessing group differences in change over time.

    Measured from blood draws before and after a one-week intervention

  • Change in Plasma Ab42/40 Ratio

    The investigators conducted a 2 (time: pre, post) × 3 (condition) ANOVA to test for an interaction effect on plasma Ab42/40 ratios. The plasma Ab42/40 ratio was calculated by dividing the plasma Ab42 concentration (pg/ml) by the plasma Ab40 concentration (pg/ml). A higher plasma Ab42/40 ratio indicates better outcome (i.e., greater brain clearance).

    Measured from blood draws before and after a one-week intervention

Secondary Outcomes (2)

  • Change in Plasma pTau-181/Tau Ratio

    Measured from blood draws before and after a one-week intervention

  • Change in Emotional Well-being

    Measured before and after a one-week intervention

Other Outcomes (1)

  • Episodic Memory

    Measured after a one-week intervention

Study Arms (3)

Belly-focus concentration meditation

EXPERIMENTAL

Participants will engage in concentration meditation for 40 minutes every day for a week while recording heart rate. They will focus on the sensations around the belly.

Behavioral: Belly-focus meditation

Belly-focus concentration meditation with slow breathing

EXPERIMENTAL

Participants will engage in concentration meditation and slow breathing for 40 minutes every day for a week while recording heart rate. They will focus on the sensations around the belly while breathing slowly.

Behavioral: Belly-focus meditation with slow breathing

No-intervention control

NO INTERVENTION

Participants will rest quietly for 40 minutes every day for a week while recording heart rate.

Interventions

Participants will engage in concentration meditation for 40 minutes every day for a week. They will focus on the sensations around the belly.

Belly-focus concentration meditation

Participants will engage in concentration meditation and slow breathing for 40 minutes every day for a week. They will focus on the sensations around the belly while breathing slowly.

Belly-focus concentration meditation with slow breathing

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Fluent in English
  • Aged between 18-35 years old
  • Agree to provide blood samples
  • Healthy adults who weigh at least 110 pounds
  • Agree to devote 40 minutes daily to this study for a week

You may not qualify if:

  • Have a disorder that would affect heart rhythm or function (e.g., abnormal cardiac rhythm, dyspnea, heart disease including coronary artery disease, angina and arrhythmia)
  • Regularly practicing any relaxation, meditation or yoga that involve breathing focused practices lasting for more than an hour each week

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Southern California

Los Angeles, California, 90089, United States

Location

MeSH Terms

Conditions

Alzheimer Disease

Condition Hierarchy (Ancestors)

DementiaBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesTauopathiesNeurodegenerative DiseasesNeurocognitive DisordersMental Disorders

Results Point of Contact

Title
Dr. Mara Mather
Organization
University of Southern California

Publication Agreements

PI is Sponsor Employee
No
Restrictive Agreement
No

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

October 20, 2023

First Posted

January 18, 2024

Study Start

January 29, 2024

Primary Completion

May 3, 2024

Study Completion

May 3, 2024

Last Updated

January 5, 2026

Results First Posted

January 5, 2026

Record last verified: 2025-12

Locations