- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06770387
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
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.
Sponsor
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- New Paradigma
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.
Clinical Trials on Lumbar Disc Surgery
-
Ankara Etlik City HospitalRecruitingMechanical Ventilation | Lumbar Disc Herniation SurgeryTurkey (Türkiye)
-
Gazi UniversityCompletedMotivational Interviewing | Nursing Care | Lumbar Disc SurgeryTurkey (Türkiye)
-
Universitaire Ziekenhuizen KU LeuvenCompletedLumbar Surgery | Radicular Pain | Fusion of Spine, Lumbar Region | Disc Herniation With Radiculopathy | Radicular Pain Related to Lumbosacral Disc Disease | Lumbar DecompressionBelgium
-
Shin Kong Wu Ho-Su Memorial HospitalTerminatedLumbar Disc Herniation | Lumbar Traction | Spinal Manipulation | Lumbar SurgeryTaiwan
-
Akdeniz UniversityCompletedLumbar Disc Herniation | Lumbar Spine SurgeryTurkey
-
Hacettepe UniversityEnrolling by invitationLumbar Disc Herniation | Lumbar Disc SurgeryTurkey (Türkiye)
-
Potsawat SurabotsoponRecruitingSurgery | Disc Degeneration | Spinal Stenosis Lumbar | Fusion of Spine | Disc DiseaseThailand
-
University Hospital, Clermont-FerrandCompletedPatients Undergoing a Lumbar Slipped Disc SurgeryFrance
-
Anesthesia Research Group UARecruitingLumbar Disc Herniation | Lumbar Spinal Stenosis | Failed Back Surgery Syndrome | Lumbar Discogenic PainUkraine
-
Providence Medical Technology, Inc.RecruitingRadiculopathy Lumbar | Degenerative Lumbar Disc DiseaseUnited States
Clinical Trials on mhealth
-
Fatima Jinnah Women UniversityNot yet recruitingType 2 Diabetes Risk Reduction in Young AdultsPakistan
-
NYU Langone HealthWeizmann Institute of Science; American Heart AssociationCompletedOverweight and Obesity | Pre-diabetesUnited States
-
Liverpool John Moores UniversityLiverpool Heart and Chest Hospital NHS Foundation Trust; University Hospitals... and other collaboratorsCompleted
-
The Hong Kong Polytechnic UniversityCompleted
-
AdventHealth UniversityRecruitingPhysical Activity | Cardiac RehabilitationUnited States
-
University of California, San FranciscoNational Institute of Mental Health (NIMH)CompletedDepressionUnited States
-
Samsung Medical CenterCompletedBreast CancerKorea, Republic of
-
NXTechNational Institute on Drug Abuse (NIDA); National Institutes of Health (NIH)Completed
-
Chin-Tsung ShenCompleted
-
Emory UniversityEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsCompleted