Investigating the effect of blended in-person and on-line supportive care on quality of life of new cases of breast cancer

Not Applicable

• Conditions: Breast cancer.; Malignant neoplasm of breast

• Registration Number: IRCT20230119057155N2
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 16 October 2023

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 70

Inclusion Criteria

Women newly diagnosed with breast cancer
Oncology specialist referral
No serious psychiatric illness
No substance abuse or addiction

Exclusion Criteria

metastasis
Participating in other treatment programs at the same time.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Hospital anxiety and depression. Timepoint: Before the intervention - after the intervention - 12 weeks after the intervention - 24 weeks after the intervention. Method of measurement: Hospital anxiety and depression scale(HADS).;Quality of life of patients. Timepoint: Before the intervention - after the intervention - 12 weeks after the intervention - 24 weeks after the intervention. Method of measurement: EORTC QLQ-C30.;Quality of life in breast cancer patients. Timepoint: Before the intervention - after the intervention - 12 weeks after the intervention - 24 weeks after the intervention. Method of measurement: (EORTC QLQ-BR23).;Supportive care needs. Timepoint: Before the intervention - after the intervention - 12 weeks after the intervention - 24 weeks after the intervention. Method of measurement: (SCNS).