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The purpose of the current trial is to study whether a support intervention based on widely used spiritual intervention could improve the quality of life of breast cancer patients in comparison to the control group or not. The target population is newly diagnosed breast cancer patients under radiation therapy who consents to participate in this study. The participants will be randomly assigned into control group receiving standard management and treatment and also routine education program or intervention group receiving both routine management/education and also an additional 6 sessions (6 weeks) educational program based on spiritual therapy intervention. The spiritual therapy sessions include: introduction, relaxation and meditation, control, identity, relationships with self, others and God, prayer therapy. The quality of life will be assessed by The specific European Organisation for Research and Treatment of Cancer quality of life group for breast cancer (EORTC BR-23 and QLQC30) and the spirituality will be assessed by FACIT-SP12.