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A Comparative Study on the Effectiveness of Meaning-Centered Pain Coping Skills Training and Mindfulness-Based Stress Reduction in Breast Cancer Patients

Not Applicable
Conditions
Breast Cancer.
Malignant neoplasm of breast
Registration Number
IRCT20230303057600N1
Lead Sponsor
Islamic Azad University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
45
Inclusion Criteria

Age range between 30 to 60 years old
Having at least a diploma
Based on clinical findings and cytology studies and doctor's diagnosis, they are diagnosed with stage 3 breast cancer and more than 6 months have passed since the diagnosis of breast cancer.
Subjects must be under chemotherapy or radiotherapy.
Subjects should not participate in other psychotherapy courses simultaneously.
They should obtain an adequate score in the Brief Pain Inventory as the baseline.

Exclusion Criteria

Having used psychedelic drugs in the past three months.
Any major mental disorder (such as psychosis, bipolar disorder, and chronic depression) or physical illness other than cancer.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Before intervention, immediately after intervention, and 45 days after intervention completion. Method of measurement: Brief pain questionnaire (BPI).;Pain self-efficacy. Timepoint: Before intervention, immediately after intervention, and 45 days after intervention completion. Method of measurement: Pain self-efficacy questionnaire (PSEQ).;Death anxiety. Timepoint: Before intervention, immediately after intervention, and 45 days after intervention completion. Method of measurement: Templer death anxiety questionnaire (DAS).;Life expectancy. Timepoint: Before intervention, immediately after intervention, and 45 days after intervention completion. Method of measurement: Schneider life expectancy questionnaire (??AHS).
Secondary Outcome Measures
NameTimeMethod
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