Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT07367074

Effect of an Educational Intervention in Women With Breast Cancer (EDU-INT-BC)

Led by Instituts Supérieurs des Professions Infirmières et Techniques de Santé, Morocco · Updated on 2026-03-03

65

Participants Needed

1

Research Sites

9 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to evaluate the effect of an educational intervention on sexual function and therapeutic adherence among women with breast cancer followed in the medical oncology department of Ibn Tofail Hospital, affiliated with Mohammed VI University Hospital Center in Marrakech. Participants will receive a structured therapeutic education program focusing on breast cancer, available treatments and their potential side effects, as well as treatment adherence and its prognostic significance. Educational sessions will be complemented by patient follow-up to reinforce key messages and support adherence. The study will assess changes in sexual function and therapeutic adherence before and after the educational intervention.

CONDITIONS

Official Title

Effect of an Educational Intervention in Women With Breast Cancer (EDU-INT-BC)

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women aged 18 years and older.
  • Diagnosed with breast cancer.
  • Receiving oral anticancer treatment.
  • Willing to participate in the study.
  • Able to attend the educational sessions.
  • Having access to a mobile phone (smartphone).
Not Eligible

You will not qualify if you...

  • Women with communication disorders.
  • Women with severe psychiatric disorders that will interfere with participation in the educational intervention.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Medical Oncology Department, Ibn Tofail Hospital, Mohammed VI University Hospital Center

Marrakesh, Marrakesh-Safi, Morocco

Actively Recruiting

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Research Team

S

Safa LAAMARI, Master Student

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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