Online Patient Navigation Program for Patients with Breast Cancer

Not Applicable

Not yet recruiting

• Conditions: Breast Cancer; Supportive Care in Cancer; Patient Navigation

• Registration Number: NCT06597773
• Lead Sponsor: Medicos e Investigadores en la Lucha contra el Cancer de Mama

Brief Summary

The goal of this prospective 1:1 randomized controlled trial is to evaluate if an online patient navigation program, designed to identify targeted supportive care needs and to facilitate referrals and web-based interventions to address these needs, can increase patients' access to supportive care services, compared to traditional in-person patient navigation providing referrals to in-person supportive care services

The main questions it aims to answer are:

* Does online patient navigation increase access to supportive care services by ≥30% among patients with breast cancer?

* Which are the barriers that hinder patients\' access to the supportive care services they require?

* What is patients\' level of satisfaction with online patient navigation?

Researchers will compare the online patient navigation program to traditional in-person patient navigation providing referrals to in-person supportive care services to assess if online patient navigation increases patients' access to supportive care services.

Participants will:

* Participate in an online or in-person patient navigation program for 4 weeks

* Answer the study surveys at baseline and 4 weeks of follow-up

Detailed Description

Not available

Study Timeline

• Status Verified: 2024-09
• Study First Submitted: 2024-09-12
• Study First Submitted QC: 2024-09-12
• Last Update Submitted: 2024-09-12
• Study First Posted: 2024-09-19
• Last Update Posted: 2024-09-19
• Study Start: 2025-07-01
• Primary Completion: 2026-02
• Study Completion: 2026-02

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: Female
• Target Recruitment: 80

Inclusion Criteria

• Female sex
• Age ≥18 years
• Diagnosis of non-metastatic breast cancer
• Internet access at home or in their mobile phone
• Availability to answer the study surveys
• Provision of signed informed consent

Exclusion Criteria

• Disease recurrence
• Inability to read or write

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Access to supportive care services	4 weeks	Participants\' rate of attendance to each of the supportive care services in study will be evaluated through a survey at 4 weeks of follow-up, which will assess each group\'s access to the recommended services, barriers encountered, and satisfaction with the navigation program.

Trial Locations

Locations (1)

Hospital Zambrano Hellion; 🇲🇽 San Pedro Garza Garcia, Nuevo Leon, Mexico