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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04290585
Other study ID # IRB13858
Secondary ID NCI-2015-02088IR
Status Completed
Phase N/A
First received
Last updated
Start date March 5, 2014
Est. completion date October 2017

Study information

Verified date February 2020
Source Fox Chase Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 160
Est. completion date October 2017
Est. primary completion date October 28, 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Questionnaire Administration
Ancillary studies
Behavioral:
Telephone-Based Intervention
Receive text message reminders

Locations

Country Name City State
United States Fox Chase Cancer Center Philadelphia Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
Fox Chase Cancer Center National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in no-show rate pre- and post-intervention 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. Baseline to up to 1 year
Secondary Acceptability of using text messaging as a reminder: survey Descriptive statistics will be used to report the results of the satisfaction survey. Up to 1 year
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