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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

A Comparative Study on the Efficacy of Meaning-Centered Pain Coping Skills Training and Mindfulness-Based Stress Reduction on Pain Levels, Pain Self-efficacy, Death Anxiety, and Life Expectancy in Breast Cancer Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230303057600N1
Enrollment
45
Registered
2023-07-08
Start date
2023-04-10
Completion date
Unknown
Last updated
2023-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer. Malignant neoplasm of breast

Interventions

Intervention 1: Intervention Group 1: They receive instruction for meaning-oriented pain coping skills for four weeks, receiving a 45- to 60-minute group session every week based on Winger and colleag

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
30 Years to 60 Years

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
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).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMina Ansari

Islamic Azad University

minaansari995@gmail.com+98 21 2288 3845

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026