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Clinical Trials/NCT04290585
NCT04290585
Completed
Not Applicable

Text for Health: Integrating Technology and Health Communication to Improve Health Outcomes (Part 2 of 2)

Fox Chase Cancer Center1 site in 1 country160 target enrollmentMarch 5, 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Female Breast Carcinoma
Sponsor
Fox Chase Cancer Center
Enrollment
160
Locations
1
Primary Endpoint
Change in no-show rate pre- and post-intervention
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This pilot clinical trial studies how well technology and health communication works in improving health outcomes in patients scheduled for mammography screening. The Mobile Mammography Screening Program provides a vital health service and it is important that all women scheduled for an appointment show-up to be screened. Technology and health communication may help decrease no-show rates among patients scheduled for mammography screening.

Detailed Description

PRIMARY OBJECTIVES: I. To decrease the mobile mammography unit no-show rate by sending text message appointment reminders to patients. II. To assess the efficacy of the text message reminders at addressing the no-show rate by collecting satisfaction survey data from patients that received the texts and that came to their scheduled appointment. OUTLINE: Patients receive 1-2 text messages a few weeks before and 1 text message 24 hours before their mammography screening appointment. Patients also receive a phone call reminder as per standard practice.

Registry
clinicaltrials.gov
Start Date
March 5, 2014
End Date
October 2017
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Appointment is at a participating location
  • Has a cell phone that can send and receive text messages
  • Agrees to receive the text messages
  • Can read either English or Spanish
  • Not yet sent text messages to 100 patients in community or corporate sites
  • Scheduled at least 1 week prior to the appointment date
  • PATIENTS FOR FOLLOW UP: come to their scheduled appointment
  • PATIENTS FOR FOLLOW UP: received the text message reminders
  • PATIENTS FOR FOLLOW UP: can read either English or Spanish

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Change in no-show rate pre- and post-intervention

Time Frame: Baseline to up to 1 year

The change (or lack of change) in the corporate sites? no-show rate will be compared to the change (or lack of change) in the community sites? no-show rate. Descriptive statistics will be used to describe the results.

Secondary Outcomes

  • Acceptability of using text messaging as a reminder: survey(Up to 1 year)

Study Sites (1)

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