MedTrace Logo

Short Message Service Based Patient Education in Spine Patients

NCT04458428 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 192

Last updated 2024-11-22

No results posted yet for this study

Summary

The investigators primary objective is to evaluate whether an SMS based patient education program improves patient satisfaction.

Conditions

  • Patient Satisfaction

Interventions

OTHER

SMS

Patients who are randomized to the intervention arm will be signed up for the automated SMS program. This cohort will receive text messages after surgery, timed from the day of discharge through 14 days post-op. Patients in this cohort will receive text messages each day. The number of text messages varies on patient interest and "yes" responses to see additional information.

Sponsors & Collaborators

Principal Investigators

  • Ryan Spiker, M.D. · University of Utah

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-07-28
Primary Completion
2024-06-03
Completion
2024-06-03

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04458428 on ClinicalTrials.gov