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

Investigating the effect of the program based on the common-sense model on illness perception and health-promoting behaviors of women with breast cancer

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230904059360N1

Enrollment

Registered

2023-09-23

Start date

2023-10-02

Completion date

Unknown

Last updated

2023-10-16

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 of unspecified site

Interventions

Intervention 1: Intervention group: In the intervention group, the intervention will be held in the form of four face-to-face sessions for 60 minutes based on the common sense model during four consec

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

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

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.

Design outcomes

Primary

Measure	Time frame
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.	—

Measure

Time frame

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.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Alidousti

Esfahan University of Medical Sciences

fatemealidoosti@nm.mui.ac.ir+98 31 3668 7153

Outcome results

None listed

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