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Mechanisms of Mindfulness Intervention: Distress Tolerance Dose Manipulation

NCT06056232 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2023-10-03

No results posted yet for this study

Summary

This study hopes to:

1. explore whether an increase in the dosage of distress tolerance intervention corresponds to greater effectiveness of mindfulness intervention in alleviating emotional distress.
2. explore whether distress tolerance mediates the effects of mindfulness intervention on alleviating emotional distress.

Conditions

  • Emotional Distress
  • Emotional Disorder

Interventions

BEHAVIORAL

Mindfulness Intervention for Emotional Distress(MIED)-normal version

Mindfulness Intervention for Emotional Distress (MIED) program provides standard audio instructions for mindfulness exercises, introduces the nature and law of anxiety, depression, and other emotions, the source of anxiety, depression, and other emotional distress, and the strategies and methods to alleviate emotional distress. These exercises, knowledge and strategies are based on the latest progress in the field of psychological counseling and treatment, and their application in daily life can help alleviate anxiety, depression and other emotional problems.

BEHAVIORAL

Mindfulness Intervention for Emotional Distress(MIED)-increase distress tolerance

Increase the intervention dose of distress tolerance in Mindfulness Intervention for Emotional Distress (MIED). For example, including more emotion exposure tasks, materials from Facing Your Feelings.

BEHAVIORAL

Mindfulness Intervention for Emotional Distress(MIED)-decrease distress tolerance

Decrease the intervention dose of distress tolerance in Mindfulness Intervention for Emotional Distress (MIED). For example, including less emotion exposure tasks and interoceptive exposure tasks.

Sponsors & Collaborators

  • Peking University

    lead OTHER

Principal Investigators

  • Xinghua Liu · School of Psychological and Cognitive Sciences, Peking University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-10-05
Primary Completion
2023-12-08
Completion
2024-03-10

Countries

  • China

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 NCT06056232 on ClinicalTrials.gov