Study Results
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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COMPLETED
NA
107 participants
INTERVENTIONAL
2024-12-24
2025-05-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
DOUBLE
Study Groups
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Control Group
No intervention, only routin care
No interventions assigned to this group
Intervention Group
Telenursing and mHealth intervention
mhealth
mobile application for postoperative period
Interventions
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mhealth
mobile application for postoperative period
Eligibility Criteria
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Inclusion Criteria
* 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
18 Years
ALL
No
Sponsors
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Hasan Kalyoncu University
OTHER
Responsible Party
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Kadiriye Pehlivan
Research Assistant
Locations
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Deva Hospital
Gaziantep, , Turkey (Türkiye)
Gaziantep University Şahinbey Research and Application Hospital
Gaziantep, , Turkey (Türkiye)
Medical Point Hospital
Gaziantep, , Turkey (Türkiye)
Kahramanmaraş Sütçü İmam University Health Practice and Research Hospital
Kahramanmaraş, , Turkey (Türkiye)
Countries
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Other Identifiers
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New Paradigma
Identifier Type: -
Identifier Source: org_study_id
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