Status:
COMPLETED
Development of an Application-Based Digital Navigator for Perioperative Breast Surgery Patients
Lead Sponsor:
M.D. Anderson Cancer Center
Conditions:
Breast
Eligibility:
All Genders
18+ years
Brief Summary
The goal of this research study is to learn how accessible JEEVA is for patients during the perioperative period (the time after the pre-operative surgical appointment, and up to 30 days after surgery
Detailed Description
Objectives: Demonstrate feasibility of use for a mobile device-based application to provide perioperative resources and support in a multimedia format to breast surgery patients Measure ease of use,...
Eligibility Criteria
Inclusion
- Subjects eligible for this study include breast surgical patients 18 years of age and older evaluated at the Texas Medical Center campus in the Nellie B Connally breast center or in the Houston Area Locations (HALs).
- This includes patients undergoing excisional biopsy, segmental mastectomy, total mastectomy, skin-sparing mastectomy, nipple-sparing mastectomy, sentinel lymphadenectomy, targeted axillary lymphadenectomy, axillary lymphadenectomy, and axillary reverse mapping.
Exclusion
- Patients who do not have a smartphone), which utilizes iOS or Android operating systems,
- Patients who have visual impairment or blindness, which precludes effective utilization of an app, will be excluded.
- Patients whose surgical planning is discussed by telephone outside of an in-person pre-operative visit, will be excluded from the study.
- Patients who have cognitive impairment will be exclude
Key Trial Info
Start Date :
February 28 2022
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
October 7 2025
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT05290402
Start Date
February 28 2022
End Date
October 7 2025
Last Update
October 14 2025
Active Locations (1)
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1
MD Anderson Cancer Center
Houston, Texas, United States, 77030