NCT04458428

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
192

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jul 2017

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 28, 2017

Completed
2.9 years until next milestone

First Submitted

Initial submission to the registry

July 1, 2020

Completed
6 days until next milestone

First Posted

Study publicly available on registry

July 7, 2020

Completed
3.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 3, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 3, 2024

Completed
Last Updated

November 22, 2024

Status Verified

November 1, 2024

Enrollment Period

6.9 years

First QC Date

July 1, 2020

Last Update Submit

November 19, 2024

Conditions

Patient Satisfaction

Keywords

Spine SurgeryShort Message Service (SMS)Patient Satisfaction

Outcome Measures

Primary Outcomes (1)

  • SpineFriend Postoperative Questionnaire

    Patient satisfaction will consist of the SpineFriend Postoperative Questionnaire

    Follow Up Visits at 2 or 6 weeks

Study Arms (2)

Control

NO INTERVENTION

No other non-standard of care activities will be performed

Intervention

EXPERIMENTAL

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

Other: SMS

Interventions

SMSOTHER

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.

Intervention

Eligibility Criteria

Age18 Years - 90 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

  • Patients under 18 years of age.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Utah Orthopedics

Salt Lake City, Utah, 84108, United States

Location

MeSH Terms

Conditions

Patient Satisfaction

Condition Hierarchy (Ancestors)

Treatment Adherence and ComplianceHealth BehaviorBehavior

Study Officials

  • Ryan Spiker, M.D.

    University of Utah

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principle Investigator

Study Record Dates

First Submitted

July 1, 2020

First Posted

July 7, 2020

Study Start

July 28, 2017

Primary Completion

June 3, 2024

Study Completion

June 3, 2024

Last Updated

November 22, 2024

Record last verified: 2024-11

Locations

US(1)