Studying the effect of mobile phone education on some complications of the disease in breast cancer patients

Studying the effect of educational intervention on fatigue and body image in breast cancer patients - Mobile Health Application

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20241015063368N1

Enrollment

104

Registered

2025-02-01

Start date

2025-03-05

Completion date

Unknown

Last updated

2025-02-03

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

Conditions

Studying the effect of educational intervention on fatigue and body image in breast cancer patients.

Interventions

Intervention 1: Intervention group: 52 people were included in this group, who were sent educational messages via messenger for 7 weeks, and completed questionnaires before the start of the interventi

Eligibility

Sex/Gender

Female

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Women 18 to 75 years old Ability to read and write A resident of Mahmudabad city Ability to communicate and understand Persian language Access to an Android or Apple smartphone Willingness to participate in the study History of breast conservation surgery or mastectomy

Exclusion criteria

Exclusion criteria: Those under 18 years of age and over 75 years of age. Those who are illiterate. Those who live in another city. Those who speak Turkish. Those who have phones other than Android or Apple phones. Those who would like to participate in other studies. Those who have a lump in the breast and are under observation.

Design outcomes

Primary

Measure	Time frame
Observation of significant changes in body image perception after intervention in the intervention group compared to the control group. Timepoint: Complete the questionnaire (before the intervention) and 49 days after the intervention and two months after the intervention. Method of measurement: Body image fear questionnaire and fatigue status assessment.	—

Secondary

Measure	Time frame
Observation of significant changes in the perception of fatigue after the intervention in the intervention group compared to the control group. Timepoint: Complete the questionnaire (before the intervention) and 49 days after the intervention and 2 months after the intervention. Method of measurement: Completing the fatigue status questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmeneh Behrozian

Shahid Beheshti University of Medical Sciences

ameneh_behrozian@yahoo.com+98 11 4308 5157

Outcome results

None listed

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