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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UNKNOWN
NA
90 participants
INTERVENTIONAL
2022-01-01
2022-09-01
Brief Summary
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Purpose in accordance with the patient's Diagnostic Information Form, diabetic foot care self-efficacy Scale(DABOO), foot care Behavior Scale(ABDO) and diabetic foot risk screening forms are available in the data collection tools; education and Research Hospital Internal Medicine outpatient clinic with Deeply Izmit Seka state hospital, inpatient or outpatient treatment for persons with Type II diabetes who agree to volunteer to participate in research 90 shall apply. After that, the groups will be divided into two groups by randomization, and one of the groups will be given training sessions consisting of min 20 max 40 minutes for diabetic foot care in 5 sessions for nine weeks. After the training, the scales will be applied to the groups again. The data obtained before and after the training will be compared statistically in a computer environment
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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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training group
training group
Trainings on diabetic foot care consisting of min 20 max 40 minutes will be given in 5 sessions for nine weeks. Training will be given face to face online.
control group
control group
Group not to be trained.
Interventions
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training group
Trainings on diabetic foot care consisting of min 20 max 40 minutes will be given in 5 sessions for nine weeks. Training will be given face to face online.
control group
Group not to be trained.
Eligibility Criteria
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Inclusion Criteria
* To be able to read and write.
* Being between the ages of 18-65.
* Being on oral antidiabetic (OAD) and/or insulin therapy.
* No restriction of access to the Internet.
* To be able to use the Zoom program or WhatsApp video conversation with or without support.
* Having computer and/or telephone skills.
* Volunteering to participate in the study (Informed consent form will be signed by the participants during the application)
* Not having sensory loss such as speech and hearing that prevents communication and no psychiatric problems.
18 Years
65 Years
ALL
Yes
Sponsors
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Maltepe University
OTHER
Responsible Party
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Ayşegül Kandemir
Principal Investigator
Locations
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Ev
Kocaeli, Izmit, Turkey (Türkiye)
Countries
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Central Contacts
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Other Identifiers
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2021/33-03
Identifier Type: -
Identifier Source: org_study_id
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