Telenursing and Transitional Care

September 9, 2025 updated by: Kadiriye Pehlivan, Hasan Kalyoncu University

Telenursing and Transitional Care After Lumbar Disc Herniation Surgery: A New Paradigm for Postoperative Care

Post-operative care for Lumbar Disc Herniation (LDH) is important to reduce postoperative complications. The transition from hospital to home after discharge is important for LDH patients, as the transition process is flawless, the necessary care is provided appropriately, and follow-up is important. The aim of the study is to determine the effects of transitional model-based telenursing and mobile application-based follow-up on fall risk, post-discharge recovery, mobility, anxiety, and complications in patients who underwent lumbar disc surgery.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

107

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Gaziantep, Turkey (Türkiye), 27027
        • Deva Hospital
      • Gaziantep, Turkey (Türkiye), 27027
        • Gaziantep University Sahinbey Research and Application Hospital
      • Gaziantep, Turkey (Türkiye), 27027
        • Medical Point Hospital
      • Kahramanmaraş, Turkey (Türkiye), 46046
        • Kahramanmaraş Sütçü İmam University Health Practice and Research Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Patients who are 18 years of age or older,
  • Can speak and understand Turkish,
  • Have no hearing, understanding, vision or speech problems,
  • Have undergone LDH surgery for the first time,
  • Have undergone LDH surgery with the open method,
  • Have not been diagnosed with depression or anxiety disorder before surgery and are not taking medication for this purpose,
  • Have a smart mobile phone suitable for taking photos or for those close to them,
  • Have not developed serious complications that would delay their discharge from the hospital,
  • Volunteer to participate in the study will be included in the study.

Exclusion Criteria:

  • Patients who wish to withdraw from the study at any stage after voluntarily participating in the study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control Group
No intervention, only routin care
Experimental: Intervention Group
Telenursing and mHealth intervention
mobile application for postoperative period

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Complication
Time Frame: From enrollment to the end of treatment at 1 weeks
developing complications
From enrollment to the end of treatment at 1 weeks
Rehospitalization
Time Frame: From enrollment to the end of treatment at 1 weeks
hospitalization in the postoperative period
From enrollment to the end of treatment at 1 weeks
Readmission
Time Frame: From enrollment to the end of treatment at 1 weeks
admission to hospital in the postoperative period
From enrollment to the end of treatment at 1 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Measuring recovery status with the Post-Discharge Surgical Recovery Scale
Time Frame: From enrollment to the end of treatment at 4 weeks
Postoperative recovery
From enrollment to the end of treatment at 4 weeks
mobilization
Time Frame: From enrollment to the end of treatment at 4 weeks
postoperative mobilization
From enrollment to the end of treatment at 4 weeks
Measurement of anxiety status with the hospital anxiety depression scale
Time Frame: From enrollment to the end of treatment at 4 weeks
Determination of change in anxiety levels between groups before discharge and one month after discharge
From enrollment to the end of treatment at 4 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 24, 2024

Primary Completion (Actual)

May 30, 2025

Study Completion (Actual)

May 30, 2025

Study Registration Dates

First Submitted

December 27, 2024

First Submitted That Met QC Criteria

January 7, 2025

First Posted (Actual)

January 13, 2025

Study Record Updates

Last Update Posted (Estimated)

September 10, 2025

Last Update Submitted That Met QC Criteria

September 9, 2025

Last Verified

September 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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