Development of an Application-Based Digital Navigator for Perioperative Breast Surgery Patients

NCT05290402 | Completed

• 2 other identifiers: 2021-1211NCI-2022-01986
• Study Type: observational
• Target: 60
• Locations: 1 country
• Sites: 1

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

Conditions

Breast

Outcome Measures

Primary Outcomes (1)

• Measure ease of use, interface and satisfaction with the electronic delivery of materials through the mobile health (mHealth) App Usability Questionnaire (MAUQ)

  through study completion, an average of 1 year

Study Arms (1)

an application-based digital navigator

JEEVA" is a new digital health navigator app. This app can be used on a mobile phone or tablet. JEEVA has all of the surgical teaching information from the traditional paper packet and also has additional resources like brief videos, checklists, and reference photos.

Other: JEEVA (new digital health navigator app)

Interventions

JEEVA (new digital health navigator app) OTHER

An app can be used on a mobile phone or tablet.

an application-based digital navigator

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

Breast Surgery Patients

You may qualify if:

• 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.

You may not qualify if:

• 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

Sponsors & Collaborators

• M.D. Anderson Cancer Center: lead

Study Sites (1)

MD Anderson Cancer Center

Houston, Texas, 77030, United States

Location

Related Links

• M D Anderson Cancer Center

Study Officials

• Christina Checka, MD

  M.D. Anderson Cancer Center

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 3, 2022
• First Posted: March 22, 2022
• Study Start: February 28, 2022
• Primary Completion: October 7, 2025
• Study Completion: October 7, 2025
• Last Updated: October 14, 2025

Record last verified: 2025-10

Locations

US (1)