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Effectiveness of mindfulness-based compassion therapy on fear of recurrence, perceived stress and hope in women with breast cancer

Effectiveness of mindfulness-based compassion therapy on fear of recurrence, perceived stress and hope in women with breast cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240611062091N1
Enrollment
30
Registered
2024-07-02
Start date
2024-07-20
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Women with breast cancer. Malignant neoplasm of breast

Interventions

Intervention 1: Intervention group: “The experimental group will receive compassion-based mindfulness therapy for 8 sessions of 90 minutes each, once a week for two months, and a one-month follow-up w
then, the experimental group will undergo psychological intervention, while the control group will not receive any intervention
following the post-test and a one-month follow-up, if the results from the experimental group are significantly positive, the control group will also undergo this therapeutic intervention in line with

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
35 Years to 50 Years

Inclusion criteria

Inclusion criteria: At least 4 months have passed since the definitive diagnosis of breast cancer with acuteness levels 1 to 3, and in the second stage of cancer. Having at least a high school diploma. Not suffering from other physical illnesses, mental disorders, and addiction. Not receiving psychological interventions (based on the patient’s file and the opinion of the relevant nurse). Completion of the consent form. The possibility of participating in group therapy sessions with the patient’s full consent. The criteria include having a minimum age of 35 and a maximum age of 50 years old.

Exclusion criteria

Exclusion criteria: A history of frequent and prolonged hospitalizations. A history of death due to cancer in the patient’s first-degree relatives. Receiving any psychological interventions and using strong painkillers (based on the patient’s medical record and the specialist doctor’s opinion).

Design outcomes

Primary

MeasureTime frame
Fear of recurrence. Timepoint: At the beginning of the study, after the end of treatment sessions, and at the 30-day follow-up stage after the end of treatment sessions. Method of measurement: Fear of Cancer Recurrence Questionnaire (Simard and Savard, 2009).;Perceived stress. Timepoint: At the beginning of the study, after the end of treatment sessions, and at the 30-day follow-up stage after the end of treatment sessions. Method of measurement: Perceived Stress Scale (PSS-14).;Hope. Timepoint: At the beginning of the study, after the end of treatment sessions, and at the 30-day follow-up stage after the end of treatment sessions. Method of measurement: Hope Scale (Snyder et al., 1991).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaba Sadri

Islamic Azad University

sabasadri1998@yahoo.com+98 913 899 1007

Outcome results

None listed

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