Mechanism of Mindfulness-Based Online Intervention in Enhancing Cognitive Flexibility

September 24, 2023 updated by: Peking University

Mechanism of Mindfulness-Based Online Intervention in Enhancing Cognitive Flexibility: Thoughts as Thoughts

Traditional offline interventions such as MBCT and MBSR have been implemented to treat patients with emotional disorders and obtained significantly improved clinical outcomes. However, these offline interventions require the involvement of a therapist expert in mindfulness and usually charge a high fee, which may not be accessible and cost-effective for lots of patients with psychological disorders. Fortunately, online self-help interventions can compensate for these disadvantages. Our research team has developed a self-help online mindfulness program targeting emotional distress (i.e., iMIED), which has been effective for individuals with emotional distress in a preliminary study. Since patients with emotional disorders usually suffer from emotional distress, the current study will apply this program to these patients, and investigate its auxiliary effects on patients' psychological and physical health.

The primary aim of the current study is to evaluate the effectiveness of iMIED for patients with emotional disorders. To do so, we will use a design in which patients who receive online mindfulness training (iMIED) except for treatment as usual (TAU) will be compared with patients who receive TAU alone. We expect the intervention to improve patients' psychopathological symptoms reported by the patients and the clinicians or the research team and increase their overall functioning, positive mental health, and physical health compared to TAU. In addition, previous studies have shown that mindfulness interventions improve psychological symptoms by improving cognitive flexibility. Therefore, the secondary aim of the study is to examine the mediating effect of cognitive flexibility on the relationships between mindfulness practice and improvements in outcome variables, and further explore the mechanism behind it.

Study Overview

Study Type

Interventional

Enrollment (Actual)

595

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Beijing
      • Beijing, Beijing, China, 100871
        • Peking University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Subjects with scores greater than 21 on the Kessler Psychological Distress Scale.

Exclusion Criteria:

  • Subjects who could not access the Internet;
  • Subjects with insufficient Chinese ability;
  • Subjects who have participated in mindfulness based projects for more than 6 weeks before, and / or the current frequency of meditation practice is more than once a week;
  • Patients with schizophrenia or psychotic affective disorder, current organic mental disorder, substance abuse disorder and generalized developmental disorder;
  • Subjects at risk of suicide.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: the TAU-only group
treatment as usual (TAU) group consisted of all medicinal and psychological treatments received between baseline and follow-up (about five months). Medicinal treatments included receiving Lorazepam, Olanzapine, Paroxetine Hydrochloride, Sertraline, etc. Psychological treatments included receiving cognitive behavior therapy or psychodynamic therapy.
Experimental: iMIED+TAU group
Internet-based Mindfulness Intervention for Emotional Distress (iMIED) program provide standard audio instructions for mindfulness exercises, introduce 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.
Internet-based Mindfulness Intervention for Emotional Distress (iMIED) program provide standard audio instructions for mindfulness exercises, introduce 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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Weekly changes of Five Facet Mindfulness Questionnaire - Short Form during the intervention
Time Frame: [Time Frame: pre-intervention; weekly during the 7-week intervention; immediately post-intervention]
The Five Facet Mindfulness Questionnaire - Short Form is a self-reported questionnaire measuring mindfulness levels. Scores range from 20 to 100, with higher scores indicating higher levels of mindfulness.
[Time Frame: pre-intervention; weekly during the 7-week intervention; immediately post-intervention]
Weekly changes of Patient Health Questionnaire during the intervention
Time Frame: [Time Frame: pre-intervention; weekly during the 7-week intervention; immediately post-intervention]

The Patient Health Questionnaire is a self-reported questionnaire measuring the degree of being troubled by various common physical symptoms. Scores range from 0 to 30.

0~4 scores: no physical symptoms; 5~9 scores: mild physical symptoms; 10~14 scores: moderate physical symptoms; 15~30 scores: severe physical symptoms.

[Time Frame: pre-intervention; weekly during the 7-week intervention; immediately post-intervention]
Weekly changes of Chinese Perceived Stress Scale during the intervention
Time Frame: [Time Frame: pre-intervention; weekly during the 7-week intervention; immediately post-intervention]
The Chinese Perceived Stress Scale is a self-reported questionnaire measuring stress. Scores range from 0 to 56, with higher scores indicating higher levels of stress.
[Time Frame: pre-intervention; weekly during the 7-week intervention; immediately post-intervention]
Weekly changes of 10-item Kessler Psychological Distress Scale during the intervention
Time Frame: [Time Frame: pre-intervention; weekly during the 7-week intervention; immediately post-intervention]
The 10-item Kessler Psychological Distress Scale is a self-reported questionnaire measuring distress. Scores range from 10 to 50, with higher scores indicating higher levels of distress.
[Time Frame: pre-intervention; weekly during the 7-week intervention; immediately post-intervention]
Weekly changes of Overall Anxiety Severity and Impairment Scale during the intervention
Time Frame: [Time Frame: pre-intervention; weekly during the 7-week intervention; immediately post-intervention]
The Overall Anxiety Severity and Impairment Scale is a self-reported questionnaire measuring anxiety. Scores range from 0 to 20, with higher scores indicating higher levels of anxiety.
[Time Frame: pre-intervention; weekly during the 7-week intervention; immediately post-intervention]
Weekly changes of Overall Depression Severity and Impairment Scale during the intervention
Time Frame: [Time Frame: pre-intervention; weekly during the 7-week intervention; immediately post-intervention]
The Overall Depression Severity and Impairment Scale is a self-reported questionnaire measuring depression. Scores range from 0 to 20, with higher scores indicating higher levels of depression.
[Time Frame: pre-intervention; weekly during the 7-week intervention; immediately post-intervention]
Weekly changes of Athens Insomnia Scale during the intervention
Time Frame: [Time Frame: pre-intervention; weekly during the 7-week intervention; immediately post-intervention]
The Athens Insomnia Scale is a self-reported questionnaire measuring sleepy quality. Scores range from 0 to 24, with lower scores indicating higher levels of sleep quality.
[Time Frame: pre-intervention; weekly during the 7-week intervention; immediately post-intervention]

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change of Beck Anxiety Inventory
Time Frame: [Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
The Beck Anxiety Inventory is a self-reported questionnaire measuring anxiety. Scores range from 0 to 63, with higher scores indicating higher levels of anxiety.
[Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
Change of Beck Depression Inventory-II
Time Frame: [Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
The Beck Depression Inventory-II is a self-reported questionnaire measuring depression. Scores range from 0 to 63, with higher scores indicating higher levels of depression.
[Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
Change of Pittsburgh sleep quality Index
Time Frame: [Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
The Pittsburgh sleep quality Index is a self-reported questionnaire measuring sleep quality. Scores range from 0 to 21, with higher scores indicating lower levels of sleep quality.
[Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
Change of Insomnia Severity Index
Time Frame: [Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
The Insomnia Severity Index is a self-reported questionnaire measuring sleep quality. Scores range from 0 to 28, with higher scores indicating lower levels of sleep quality.
[Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
Change of Mindful Attention Awareness Scale
Time Frame: [Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
The Mindful Attention Awareness Scale is a self-reported questionnaire measuring mindfulness levels. Scores range from 15 to 90, with higher scores indicating higher levels of mindfulness.
[Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
Change of Quality of Relationship Index
Time Frame: [Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
The Quality of Relationship Index is a self-reported questionnaire measuring relationship quality. Scores range from 7 to 42, with higher scores indicating higher levels of relationship quality.
[Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
Change of Interpersonal Reactivity Index-C
Time Frame: [Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
The Interpersonal Reactivity Index-C is a self-reported questionnaire measuring interpersonal reactivity. Scores range from 0 to 88, with higher scores indicating higher levels of interpersonal reactivity.
[Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
Change of Intimacy Check and Evaluation Scale
Time Frame: [Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
The Intimacy Check and Evaluation Scale is a self-reported questionnaire measuring relationship intimacy. Scores range from 5 to 105, with higher scores indicating higher levels of relationship intimacy.
[Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
Moderation effect and possible changes of the Experience Questionnaire
Time Frame: [Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
The Experience Questionnaire is a self-reported questionnaire measuring decentering ability. Scores range from 20 to 100, with higher scores indicating higher levels of decentering ability.
[Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
Moderation effect and possible changes of the Emotion Regulation Questionnaire
Time Frame: [Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
The Experience Questionnaire is a self-reported questionnaire measuring emotion regulation ability. Scores range from 7 to 70, with higher scores indicating higher levels of emotion regulation ability.
[Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
Moderation effect and possible changes of the Cognitive Flexibility Inventory
Time Frame: [Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
The Cognitive Flexibility Inventory is a self-reported questionnaire measuring cognitive flexibility level. Scores range from 5 to 100, with higher scores indicating higher levels of cognitive flexibility.
[Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
Moderation effect and possible changes of the Thoughts as Thoughts Scale
Time Frame: [Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
The Thoughts as Thoughts Scale is a self-reported questionnaire measuring treating thoughts as thoughts ability. Scores range from 6 to 30, with higher scores indicating higher levels of treating thoughts as thoughts ability.
[Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
Moderation effect and possible changes of the Scale of Life Engagement
Time Frame: [Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
The Scale of Life Engagement is a self-reported questionnaire measuring life engagement. Scores range from 0 to 56, with higher scores indicating higher levels of life engagement.
[Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
Moderation effect and possible changes of the Self-Compassion Scale
Time Frame: [Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
The Self-Compassion Scale is a self-reported questionnaire measuring self- compassion. Scores range from 26 to 130, with higher scores indicating higher levels of self- compassion.
[Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
Moderation effect and possible changes of the Rumination- Reflection Questionnaire
Time Frame: [Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]
The Rumination- Reflection Questionnaire is a self-reported questionnaire measuring rumination- reflection level. Scores range from 5 to 60, with higher scores indicating higher levels of rumination- reflection.
[Time Frame: pre-intervention; 3 weeks into intervention; 5 weeks into intervention; immediately post-intervention]

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Xinghua Liu, School of Psychological and Cognitive Sciences, Peking University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 18, 2023

Primary Completion (Estimated)

February 28, 2024

Study Completion (Estimated)

February 28, 2024

Study Registration Dates

First Submitted

September 6, 2023

First Submitted That Met QC Criteria

September 6, 2023

First Posted (Actual)

September 13, 2023

Study Record Updates

Last Update Posted (Actual)

September 28, 2023

Last Update Submitted That Met QC Criteria

September 24, 2023

Last Verified

September 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • E20230905

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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