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Telenursing and Transitional Care

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06770387
Enrollment
107
Registered
2025-01-13
Start date
2024-12-24
Completion date
2025-05-30
Last updated
2025-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lumbar Disc Surgery

Keywords

mHealth, telenursing, transitional care, lumbar disc surgery, complications

Brief summary

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.

Interventions

BEHAVIORALmhealth

mobile application for postoperative period

Sponsors

Hasan Kalyoncu University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
ComplicationFrom enrollment to the end of treatment at 1 weeksdeveloping complications
RehospitalizationFrom enrollment to the end of treatment at 1 weekshospitalization in the postoperative period
ReadmissionFrom enrollment to the end of treatment at 1 weeksadmission to hospital in the postoperative period

Secondary

MeasureTime frameDescription
Measuring recovery status with the Post-Discharge Surgical Recovery ScaleFrom enrollment to the end of treatment at 4 weeksPostoperative recovery
mobilizationFrom enrollment to the end of treatment at 4 weekspostoperative mobilization
Measurement of anxiety status with the hospital anxiety depression scaleFrom enrollment to the end of treatment at 4 weeksDetermination of change in anxiety levels between groups before discharge and one month after discharge

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026