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THE EFFECT OF ONLINE TRAINING ON FOOT CARE

M

Maltepe University

Status

Enrolling

Conditions

Diabetic Foot
Type2diabetes

Treatments

Other: control group
Other: training group

Study type

Interventional

Funder types

Other

Identifiers

NCT05473494
2021/33-03

Details and patient eligibility

About

The aim of this study is to determine the effect of online trainings on diabetic foot care on foot care behavior and self-efficacy attitudes of individuals with type II diabetes.

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

Enrollment

90 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients who were applied the Dietetic Foot Risk Screening form during the physician's examination and who were in the low and medium risk groups after the physician's examination.
  • 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.

Exclusion criteria

outside the inclusion criteria.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

90 participants in 2 patient groups

training group
Experimental group
Treatment:
Other: training group
control group
Active Comparator group
Treatment:
Other: control group

Trial contacts and locations

1

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Central trial contact

Ayşegül Kandemir

Data sourced from clinicaltrials.gov

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