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CompletedNCT04458428SMSUpdated Nov 22, 2024

Short Message Service Based Patient Education in Spine Patients

An interventional study of SMS in Patient Satisfaction, sponsored by University of Utah. Completed at 1 site in United States. Open to participants aged 18 Years to 90 Years. Per ClinicalTrials.gov, last updated 2024-11-22.

Sponsored by University of Utah · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 2 years 11 months after the study started (first participant enrolled Jul 2017, registered Jul 2020).
Phase
Not applicable
Study type
Interventional
Enrollment
192
Allocation
Randomized
Ages
18 Years to 90 Years
Sex
All
01

Study summary

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

Read the detailed description

Back and neck related complaints effect as much as 11% of the U.S. population and are one of the most common presenting complaints at health care visits. A small subset of these patients receive spine surgery of various types in the hopes of alleviating symptoms that are recalcitrant to conservative management. The utilization of spine surgery has been rapidly increasing.2 An estimated 413,000 spinal fusions were performed in the U.S. in 2008 accounting for almost $34 billion in charges.

Patient satisfaction has become an increasingly important measure of healthcare quality. This paradigm shift is evident in the changing reimbursement models used by the Centers for Medicare and Medicaid Services (CMS). Hospital Consumer Assessment of Healthcare Providers and Systems (HCAHPS) is a survey-based assessment of patient satisfaction that was initially developed in 2002. Currently, HCAHPS provides the ability to compare patient satisfaction with the care they receive at various healthcare systems across the country. These scores are used as part of a value-based purchasing initiative that can lead to a hospital gaining or losing as much as 1.5% of their annual medicare revenue as a result of patient satisfaction based incentives. This presents an important opportunity to optimize patient satisfaction in order to both improve patient care and preserve hospital income.

A number of novel text-message based applications have been developed for healthcare use in various settings. In the surgical setting text messaging has been used to provide pre-operative education modules, as well as to track medication adherence after transplant. This study aims to develop and critically evaluate, a text-messaging based patient education system aimed at improving patient satisfaction with the post-operative course after spine surgery.

02

Conditions studied

  • Patient Satisfaction

Keywords

  • Spine Surgery
  • Short Message Service (SMS)
  • Patient Satisfaction
03

In context

Lead sponsor

University of Utah is the lead sponsor of 969 studies on the registry; 178 are open to participants now.

Of its 107 completed or terminated interventional studies of FDA-regulated products, 62 (58%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients 18 years and over undergoing spine surgery at the University of Utah

Exclusion criteria

Exclusion Criteria:

  • Patients under 18 years of age.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
192 participants (actual)

Study arms

  • No intervention
    Control

    No other non-standard of care activities will be performed

  • Experimental
    Intervention

    Will be signed up for the automated short message service (SMS)

    Other: SMS

Interventions

  • OtherSMS

    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.

06

What researchers measure

Primary outcomes

  1. SpineFriend Postoperative Questionnaire

    Patient satisfaction will consist of the SpineFriend Postoperative Questionnaire

    Time frame: Follow Up Visits at 2 or 6 weeks

07

Study locations

1 site
  • University of Utah Orthopedics
    Salt Lake City, Utah 84108, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 22, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04458428
Lead sponsor
University of Utah
Responsible party
Ryan Spiker (Principle Investigator, University of Utah) — Principal investigator
First posted
Jul 7, 2020
Start date
Jul 28, 2017
Primary completion
Jun 3, 2024
Completion
Jun 3, 2024
Last update
Nov 22, 2024

Study contacts

Ryan Spiker, M.D.
principal investigator · University of Utah

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2024. You cannot join it, but the record below documents what was studied.

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