MindVybe tVNS/APS for Wellbeing in Breast Cancer Survivors
NCT07782866 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 46
Last updated 2026-08-24
Summary
This study tests whether a gentle, non-invasive device called mindvybe can help improve feelings of wellbeing in people who have had breast cancer. Mindvybe delivers mild electrical stimulation near the vagus nerve (on the ears and neck) and to specific points on the earlobes.
About 60 adults (ages 18-75) who finished breast cancer treatment within the past five years and still have ongoing wellbeing problems (such as low mood, stress, fatigue, or sleep issues) will take part. Participants will receive five 50-minute mindvybe sessions over one week. Researchers will measure changes in wellbeing, distress, fatigue, sleep, and heart-rate patterns before, during, and for up to 12 weeks after the sessions.
The study is open-label (everyone receives the same treatment) and is considered low-risk.
Conditions
Interventions
- DEVICE
-
Transcutaneous vagus nerve and acupuncture point stimulation
Non-invasive transcutaneous stimulation delivered to the skin near the auricular and cervical branches of the vagus nerve and to acupuncture points on both earlobes using ultra-low electrical current. Participants receive five 50-minute sessions over a 7-day period.
Sponsors & Collaborators
-
The Healing Consciousness Foundation
lead OTHER
Study Design
- Allocation
- NA
- Purpose
- SUPPORTIVE_CARE
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-04-14
- Primary Completion
- 2026-07-24
- Completion
- 2026-07-24
Countries
- United States
Study Locations
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