Telenursing and Transitional Care

NCT ID: NCT06770387

Last Updated: 2025-09-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

107 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-12-24

Study Completion Date

2025-05-30

Brief Summary

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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.

Detailed Description

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Conditions

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Lumbar Disc Surgery

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

DOUBLE

Participants Caregivers

Study Groups

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Control Group

No intervention, only routin care

Group Type NO_INTERVENTION

No interventions assigned to this group

Intervention Group

Telenursing and mHealth intervention

Group Type EXPERIMENTAL

mhealth

Intervention Type BEHAVIORAL

mobile application for postoperative period

Interventions

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mhealth

mobile application for postoperative period

Intervention Type BEHAVIORAL

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hasan Kalyoncu University

OTHER

Sponsor Role lead

Responsible Party

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Kadiriye Pehlivan

Research Assistant

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Deva Hospital

Gaziantep, , Turkey (Türkiye)

Site Status

Gaziantep University Şahinbey Research and Application Hospital

Gaziantep, , Turkey (Türkiye)

Site Status

Medical Point Hospital

Gaziantep, , Turkey (Türkiye)

Site Status

Kahramanmaraş Sütçü İmam University Health Practice and Research Hospital

Kahramanmaraş, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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New Paradigma

Identifier Type: -

Identifier Source: org_study_id

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