Investigating the effect of the program based on the common-sense model on breast cancer

Not Applicable

Recruiting

• Conditions: Breast cancer.; Malignant neoplasm of breast of unspecified site; C50.9

• Registration Number: IRCT20230904059360N1
• 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: Recruiting
• Sex: Female
• Target Recruitment: 72

Inclusion Criteria

According to the pathology sheet, the diagnosis of breast cancer has been established for the patient.
The patient should be aware of the diagnosis of her disease.
The patient must be at least 18 years old.
The patient has the ability to speak and communicate verbally.
The patient must be able to read and write in Farsi at least to complete the questionnaire.
At least two months and a maximum of one year have passed since the active treatment of breast cancer.
According to pathology documentation, the disease was diagnosed in stages I to IIIA.

Exclusion Criteria

According to the medical file documentation, the patient has a history of psychiatric illness requiring hospitalization or drug treatment.
There is a family history of breast cancer in the patient's first degree family (mother, sister, father and brother) based on the question of the patient.
The patient does not consent to participate in the research.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The score of illness perception in the Brief Illness Perception Questionnaire (Brief IPQ). Timepoint: Illness perception is checked before the start of the study and eight weeks after the start of the study. Method of measurement: Brief Illness Perception Questionnaire (Brief IPQ).;The score of health promoting behaviors from the Health Promoting Behaviors Questionnaire (HPLPII). Timepoint: Health-promoting behaviors before the intervention and eight weeks after the start of the intervention are measured through a questionnaire. Method of measurement: Health Promoting Lifestyle Profile-II (HPLP-II) Questionnaire.