Mindfulness Training Improves Emotions Among Female Abdominal Cancer Patients

May 2, 2025 updated by: Kou Hui, Zunyi Medical College

Mindfulness Training Improves Depression Among Female Abdominal Cancer Patients Through Improving Cognitive Emotion Regulation and Emotional State

We first explored the effect of mindfulness training on depression in patients with abdominal cancer. Then the effects of cognitive emotion regulation and emotional state in the training effect were examined. Sixty patients with abdominal cancer were recruited from a hospital and divided into two groups: the mindfulness group (n=30) who received a four-week mindfulness training program, and the control group (n=30) who received only one mindfulness lecture. All participants were assessed using the Mindful Attention Awareness Scale, Cognitive Emotion Regulation Strategy Questionnaire, Positive and Negative Affect Scale, and depression subscale of the Patient Health Questionnaire before and after the mindfulness training program.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Participants Sixty patients with abdominal cancer from a hospital were recruited. All patients were divided into a mindfulness group (n=30) who received a four-week mindfulness training program and a control group (n=30) who received only one mindfulness lecture over four weeks. No age difference was found between the mindfulness group (M=53.87, SD=10.31, ranging from 35 to 75) and the control group (M=52.73, SD=7.27, ranging from 42 to 69), t(58) =0.49, p=0.625. The participants were all women and none of them reported a history of neurological or psychiatric illness.

Ethics approval statement All procedures involving human participants in this study were conducted in strict accordance with the ethical standards of the Ethical Committee at a medical university, as well as the 1964 Helsinki Declaration and its subsequent amendments, or any comparable ethical standards. All participants gave informed consent before participating. Furthermore, following the completion of the study, the control group could also undergo the same mindfulness training program if they volunteered.

Measurements Mindful Attention Awareness Scale. It contains 15 items in a single dimension. All of the items are rated on a 7-point Likert scale from 1 ("strongly agree") to 7 ("strongly disagree"). Higher scores reflect a higher level of trait mindfulness and awareness of the present moment. The Cronbach's α was 0.89 and the two-week test-retest reliability was 0.87 in the Chinese sample. The Cronbach's α coefficient of the scale in the present study was 0.87.

The Patient Health Questionnaire. Its depression subscale consists of 9 items. All of the items are rated on a 4-point Likert scale from 1 ("strongly disagree") to 4 ("strongly agree"). Higher scores indicate a greater level of depression. The Cronbach's α was 0.86 and the two-week test-retest reliability was 0.86 in the Chinese sample. The Cronbach's α coefficient of the scale in the present study was 0.87.

The Cognitive Emotion Regulation Questionnaire. It consists of 36 items and nine subscales. These subscales assess various strategies employed in cognitive emotion regulation, such as self-blame, blaming others, acceptance, refocus on planning, positive refocusing, rumination or focus on thought, positive reappraisal, putting into perspective, and catastrophizing. Each item is rated on a 5-point Likert scale ranging from 1 ("strongly disagree") to 5 ("strongly agree"). Higher scores on each subscale indicate a greater likelihood of utilizing that particular cognitive emotion regulation strategy in the face of negative events. Adaptive cognitive emotion regulation strategy is assessed using the sum of scores on the acceptance, putting into perspective, refocus on planning, positive refocusing, and positive reappraisal subscales. Non-adaptive cognitive emotion regulation strategy is assessed using the sum of scores on the self-blame, blaming others, rumination or focus on thought, and catastrophizing subscales. In the Chinese samples, the Cronbach's α coefficients for these subscales ranged from 0.48 to 0.89. The Cronbach's α coefficients of the adaptive and non-adaptive cognitive emotion regulation strategies subscales in the present study were 0.84 and 0.74 respectively.

The Positive and Negative Affect Scale. It contains 20 items and consists of two self-report subscales including positive emotions and negative emotions. All of the items are rated on a 5-point Likert scale from 1 ("strongly disagree") to 5 ("strongly agree"). The higher the score, the stronger the emotions in a certain dimension. The Cronbach's α for positive and negative emotions were 0.85 and 0.83 respectively in the Chinese sample. The Cronbach's α coefficients of the positive and negative emotions subscales in the present study were 0.84 and 0.78 respectively.

Procedure There are three phases in the present study, i.e., the pre-training test phase (T1), the training phase, and the post-training test phase (T2). In the two test phases, all participants completed all the questionnaires including the Mindful Attention Awareness Scale, the Patient Health Questionnaire-depression subscale, the Cognitive Emotion Regulation Questionnaire, and the Positive and Negative Affect Scales.

The mindfulness training program consisted of four 45-minute lessons, conducted once a week. After each lesson, participants were required to complete daily homework, which included the mindfulness exercises learned during that week for at least 30 minutes. The control group only attended a mindfulness lecture during the four weeks.

The mindfulness training program was based on Kabat-Zinn's Mindfulness-Based Stress Reduction5 and Williams' Mindfulness-Based Cognitive Therapy. Additionally, specific contents of cancer-related mindfulness training were incorporated into this program, such as Anti-cancer Self-healing Power: 8 Lessons in Mindfulness-based Stress Reduction. The contents of the mindfulness training program included:

Session 1: Establishing a connection with the body. Mindfulness activities consisted of eating one raisin mindfully and mindfulness cobble practice.

Session 2: Observing thoughts as they are. Mindfulness activities included the body scan and awareness of breathing meditation.

Session 3: Cultivating mindful attention. Mindfulness activities involved awareness of breathing meditation and mindfulness compassion meditation.

Session 4: Applying mindfulness in daily life. Mindfulness activities included embracing yourself, 3-min breathing space and mindfulness stretching exercises.

Statistical analysis To investigate the impact of mindfulness training on mental states, we conducted a 2 (Group: mindfulness group and control group) × 2 (Test time: T1 and T2) repeated measures ANOVA on each scale score. If a significant interaction effect or main effect was observed, post hoc analysis with Bonferroni correction was performed. To examine the role of cognitive emotion regulation strategy in improving emotional symptoms, we constructed multiple mediation models based on previous studies. First, we calculated the improvements in all measurements by subtracting the scores at T1 from the scores at T2 (i.e., improvement=T2-T1). Next, we examined bivariate correlations between each two improvements. Finally, we treated mindfulness training (0=control group, 1=training group) as the independent variable, the improvement in depressive symptoms as the dependent variable, and the improvements in cognitive emotion regulation strategy and positive/negative emotions as the mediators. We utilized the PROCESS v4.1 macro for SPSS (Model 6) to test the mediation effects.

Study Type

Interventional

Enrollment (Actual)

60

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

    • Guizhou
      • Zunyi, Guizhou, China, 563000
        • Zunyi Medical 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:

  • patients with abdominal cancer; female; over 19 years old

Exclusion Criteria:

  • a history of neurological or psychiatric illness; intellectual or speech disorders

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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: mindfulness group
Received a four-week mindfulness training program.
The mindfulness training program consisted of four 45-minute lessons, conducted once a week. After each lesson, participants were required to complete daily homework, which included the mindfulness exercises learned during that week for at least 30 minutes. The mindfulness training program was based on Kabat-Zinn's Mindfulness-Based Stress Reduction and Williams' Mindfulness-Based Cognitive Therapy. Additionally, specific contents of cancer-related mindfulness training were incorporated into this program, such as Anti-cancer Self-healing Power: 8 Lessons in Mindfulness-based Stress Reduction.
No Intervention: control group
Received only one mindfulness lecture over four weeks. Following the completion of the study, the control group could also undergo the same mindfulness training program if they volunteered.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The change from baseline Mindful Attention Awareness Scale at post-training
Time Frame: Baseline (Day 0)/Post-training (Month 1)
It contains 15 items in a single dimension. All of the items are rated on a 7-point Likert scale from 1 ("strongly agree") to 7 ("strongly disagree"). Higher scores reflect a higher level of trait mindfulness and awareness of the present moment.
Baseline (Day 0)/Post-training (Month 1)
The change from baseline Patient Health Questionnaire at post-training
Time Frame: Baseline (Day 0)/Post-training (Month 1)
Its depression subscale consists of 9 items. All of the items are rated on a 4-point Likert scale from 1 ("strongly disagree") to 4 ("strongly agree"). Higher scores indicate a greater level of depression.
Baseline (Day 0)/Post-training (Month 1)
The change from baseline Cognitive Emotion Regulation Questionnaire at post-training
Time Frame: Baseline (Day 0)/Post-training (Month 1)
It consists of 36 items and nine subscales. These subscales assess various strategies employed in cognitive emotion regulation, such as self-blame, blaming others, acceptance, refocus on planning, positive refocusing, rumination or focus on thought, positive reappraisal, putting into perspective, and catastrophizing. Each item is rated on a 5-point Likert scale ranging from 1 ("strongly disagree") to 5 ("strongly agree"). Higher scores on each subscale indicate a greater likelihood of utilizing that particular cognitive emotion regulation strategy in the face of negative events.
Baseline (Day 0)/Post-training (Month 1)
The change from baseline Positive and Negative Affect Scale at post-training
Time Frame: Baseline (Day 0)/Post-training (Month 1)
It contains 20 items and consists of two self-report subscales including positive emotions and negative emotions. All of the items are rated on a 5-point Likert scale from 1 ("strongly disagree") to 5 ("strongly agree"). The higher the score, the stronger the emotions in a certain dimension.
Baseline (Day 0)/Post-training (Month 1)

Collaborators and Investigators

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

Investigators

  • Study Director: Taiyong Bi, PhD, Zunyi Medical College

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)

August 1, 2024

Primary Completion (Actual)

December 30, 2024

Study Completion (Actual)

December 30, 2024

Study Registration Dates

First Submitted

June 19, 2024

First Submitted That Met QC Criteria

June 19, 2024

First Posted (Actual)

June 25, 2024

Study Record Updates

Last Update Posted (Actual)

May 7, 2025

Last Update Submitted That Met QC Criteria

May 2, 2025

Last Verified

May 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • ZunyiMP

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

only IPD used in the results publication

IPD Sharing Time Frame

6/20/2024-6/20/2029

IPD Sharing Access Criteria

Anonymized data can be shared upon reasonable request by the corresponding author.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ANALYTIC_CODE

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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