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Mindfulness Intervention for Maltreatment-Related Cognitive Decline

NCT07066800 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 104

Last updated 2025-07-15

No results posted yet for this study

Summary

The goal of this clinical trial is to examine whether an online mindfulness-based training program can help improve cognitive function including attention, emotional regulation, and mental health (such as depression and anxiety) in young adults (ages 19 to 40) who have experienced maltreatment. The main questions it aims to answer are:

* Can a 4-week online mindfulness program improve cognitive function including attention in adults with a history of maltreatment?
* Does the program reduce symptoms of depression and anxiety compared to a control group?

Researchers will compare a mindfulness training group with a waiting-list control group to see if the intervention leads to improvements in psychological and cognitive functioning.

Participants will:

* Complete psychological and cognitive assessments before and after the 4-week period
* Watch weekly online educational and mindfulness practice videos (e.g., breathing, body scan, walking meditation)
* Perform weekly mindfulness-based assignments through a study website
* Engage in optional interaction via a chat channel

Conditions

  • Health Adult Subjects
  • Maltreament

Interventions

BEHAVIORAL

Mindfulness-Based Online Training Program

A 4-week web-based mindfulness program developed by the research team, designed to improve attention, emotional regulation, and mental health in adults with a history of maltreatment. * The intervention includes: * Weekly educational videos (5-10 minutes each) * Weekly mindfulness practice videos (5-10 minutes each) * Assigned home practices each week * Optional support via KakaoTalk channel for Q\&A and participant engagement * Weekly themes include: * Breathing and muscle relaxation * Mindfulness breathing meditation * Body scan meditation * Mindful walking

Sponsors & Collaborators

  • Kyungpook National University Chilgok Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-06-27
Primary Completion
2026-02-28
Completion
2027-02-28

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07066800 on ClinicalTrials.gov