Actively Recruiting
Online Mindfulness-based Stress Reduction for Patients Receiving Chemotherapy
Led by Medicos e Investigadores en la Lucha contra el Cancer de Mama · Updated on 2025-09-26
200
Participants Needed
1
Research Sites
30 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this prospective, waitlist-controlled, 1:1 randomized study is to evaluate if an online mindfulness-based stress reduction (MBSR) intervention reduces treatment-related stress levels among patients with breast cancer receiving chemotherapy. The main questions it aims to answer are: * Does an online MBSR intervention reduce stress levels (measured through the Perceived Stress Scale) among participants? * Does an online MBSR intervention reduce anxiety, depression, insomnia, fatigue, nausea, diarrhea, constipation, pain, and peripheral neuropathy (measured through the PRO-CTCAE of the National Cancer Institute) among participants? Researchers will compare the online MBSR intervention to no intervention to see if online MBSR reduces treatment-related stress. Participants will: * Participate in an online MBSR intervention or no intervention for 6 weeks * Answer the study surveys at baseline, 7 weeks, and 11 weeks of follow-up
CONDITIONS
Official Title
Online Mindfulness-based Stress Reduction for Patients Receiving Chemotherapy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female sex
- Age 618 years
- Diagnosis of non-metastatic breast cancer
- Plan to start neoadjuvant or adjuvant chemotherapy in less than 4 weeks
- Internet access at home or on their mobile phone
- Availability to participate in the online MBSR intervention for 6 weeks
- Availability to answer the study surveys
- Provision of signed informed consent
You will not qualify if you...
- Disease recurrence
- Current meditation or mindfulness practice
- Inability to read or write
AI-Screening
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Trial Site Locations
Total: 1 location
1
Hospital Zambrano Hellion
San Pedro Garza García, Nuevo León, Mexico, 66278
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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