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Effects of Mindfulness-based Intervention on Epigenetic Mechanisms, Cognition Function, Stress Response, and Well-being

U

University of Sao Paulo General Hospital

Status

Completed

Conditions

Learning and Memory
DNA Methylation
Mindfulness
Psychological Well-being
Stress

Treatments

Other: Active control
Other: Mindfulness meditation training

Study type

Interventional

Funder types

Other

Identifiers

NCT05085847
3.159.669

Details and patient eligibility

About

The purpose of this study is to assess the effect of a mindfulness-based intervention on DNAmethylation, cognitive functions, stress response, and well-being in healthy female adults.

Full description

After being informed about the study and potential risks, all volunteers giving written informed consent will undergo a 1-3 week screening period to determine eligibility for study entry. At week 0, volunteers who meet the eligibility requirements will be randomized in a 1:1 ratio to the active control group (8-week, 2 hours/week of lectures) or mindfulness-based intervention (8-week, 2 hours/week of mindfulness meditation training).

Enrollment

100 patients

Sex

Female

Ages

23 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • (1) Brazilian male or female aged between 23 and 65 years and (2) currently working in the classroom

Exclusion criteria

  1. clinical diagnosis of depression
  2. clinical diagnosis of anxiety disorders
  3. clinical diagnosis of schizophrenia
  4. report of an infectious condition in the last 15 days before collecting a blood sample;
  5. had previously practiced or currently practicing meditation, yoga or Tai-Chi.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

100 participants in 2 patient groups

Mindfulness-based intervention (MBI)
Experimental group
Description:
Participants received mindfulness training for 8 weeks (two-hour meetings; 16 hours total)
Treatment:
Other: Mindfulness meditation training
Active control group
Active Comparator group
Description:
Participants received lectures for 8 weeks (two-hour meetings; 16 hours total)
Treatment:
Other: Active control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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