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Impact Of Orem’s Supportive-Educative System in mastectomized women

Investigating the Impact Of Orem’s Supportive-Educative System On Depression, Body Image And Self-Esteem Of Women Underwent a Mastectomy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20140212016564N16
Enrollment
80
Registered
2022-09-07
Start date
2022-09-23
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Breast cancer, mastectomy. Malignant neoplasm of breast

Interventions

Intervention 1: Intervention group: According to the theory of Orem nursing systems, it will be held as a support-educational system in 4 stages (diagnostic, PRESCRIPTIVE, regulatory, and control ope

Sponsors

Oroumia University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
35 Years to 65 Years

Inclusion criteria

Inclusion criteria: Women who have started at least one session of chemotherapy. Women whose chemotherapy sessions will continue for at least another 3 months. Women who have undergone mastectomy surgery (total or partial) within the last 5 months. No history of other malignancies (according to the patient's statement and medical record) Not suffering from chronic diseases (according to the patient's statement and medical record) Absence of other stressful events such as the death of a first degree relative in the last 6 months according to the patient statement Not suffering from hearing, vision and cognitive disorders (according to the statement of the patient and companion) Ability to speak Persian or Turkish Ability to complete the questionnaire Willingness to participate in the study Not having specific psychological disorders such as major depression (according to the patient's statement and medical record) Not using drugs or psychotropic substances (according to the patient's statement and medical record) Not taking drugs that affect the physical and mental state (according to the patient's statement and medical record) Access to smart phone and internet

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Depression score in Beck questionnaire. Timepoint: At the beginning of the study, immediately after the end of the intervention, one month, three months and six after the Imam of the intervention. Method of measurement: Beck's Depression Inventory-II.;Body image score of women with breast cancer in Hopwood questionnaire. Timepoint: At the beginning of the study, immediately after the end of the intervention, one month, three months and six after the Imam of the intervention. Method of measurement: Hopwood body image scale (BIS) of women with breast cancer.;Self-esteem score in the Rosenberg questionnaire. Timepoint: At the beginning of the study, immediately after the end of the intervention, one month, three months and six after the Imam of the intervention. Method of measurement: Rosenberg's Self-Esteem Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMoloud Radfar

Oroumia University of Medical Sciences

radfar.m@umsu.ac.ir+98 44 3275 4962

Outcome results

None listed

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