The Effects of Video Training Given to Individuals With Type 2 Diabetes

December 24, 2023 updated by: İlknur METİN AKTEN, Kırklareli University

The Effects of Video Training Given to Individuals With Type 2 Diabetes Through Smartphones on Self-Care and Metabolic Control

The goal of this randomised control type of study is to examine the effects of Video Diabetes Training given to individuals with Type 2 Diabetes through smartphones on self-care and metabolic control.

The Hypotheses of the Study:

H1: Video Diabetes Training given to individuals with Type 2 Diabetes through smartphones has a positive impact on individuals' self-care.

H2: Video Diabetes Training given to individuals with Type 2 Diabetes through smartphones has a positive impact on individuals' metabolic control variables.

Participants will answer the data collection tools in the first and second interviews and metabolic control variables will be record. Diabetes training videos will sent to the Training Group through smartphones after the first meeting as two episodes a week.

Video Diabetes Training given to training group will be examine the effects of on self-care and metabolic control.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

The study will conduct to examine the effects of Video Diabetes Training given to individuals with Type 2 Diabetes through smartphones on self-care and metabolic control.

This experimental, randomized, and controlled study will conduct with a total of 112 individuals with Type 2 Diabetes (56 in the Training Group, and 56 in the Control Group), who apply to the Internal Medicine Clinic of a state hospital in the Mediterranean Region of Turkey between February and August 2022, who volunteered to participate in the study and met the inclusion criteria.

A total of 112 individuals with Type 2 Diabetes, who volunteered to participate in the study, and met the inclusion criteria, will select with the Simple Random Sampling Method and will randomize with the help of a computer program.

Participants will answer the data collection tools in the first and second interviews and metabolic control variables will be record. Diabetes training videos will sent to the Training Group through smartphones after the first meeting as two episodes a week.

Video Diabetes Training given to training group will be examine the effects of on self-care and metabolic control.

Study Type

Interventional

Enrollment (Actual)

112

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Kırklareli, Turkey, 39100
        • Kırklareli University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • agreed to participate in the study voluntarily,
  • were diagnosed with Type 2 Diabetes for at least 6 months,
  • were 18 years of age or older,
  • were literate, had smartphones with video playback features and internet,
  • without a physician diagnosis that would prevent communication, and psychiatric problems and hearing problems
  • those who did not have sensory losses such as vision or hearing.

Exclusion Criteria:

-Individuals who did not meet the inclusion criteria.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Video Diabetes Training group

The data collection tools will apply in the first and second interviews and metabolic control variables will record.

Diabetes training videos will sent to the Training Group through smartphones after the first meeting as two episodes a week.

The participants in the Training Group is to sent a total of eight episodes of the Diabetes Training Videos prepare by the researcher, twice a week, through smartphones after the first interview
No Intervention: control group
The data collection tools will apply in the first and second interviews and metabolic control variables will record.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Diabetes Self-Care Scale mean score
Time Frame: At the first interview (baseline) and at the second interview 3 months later
The comparison of Diabetes Self-Care Scale pre-test, post-test and change difference values between training and control groups. The lowest acceptable level of the scale is 92 points. The highest score that can be obtained from the scale is 140 points. As the score of the scale increases, patients' self-care activities also increase positively.
At the first interview (baseline) and at the second interview 3 months later
Fasting plasma glucose value
Time Frame: At the first interview (baseline) and at the second interview 3 months later

Comparison of fasting plasma glucose variables between training and control groups.

Fasting plasma glucose (mg/dl) value was obtained as a result of the participant's routine blood test.

At the first interview (baseline) and at the second interview 3 months later
HbA1c value
Time Frame: At the first interview (baseline) and at the second interview 3 months later
Comparison of HbA1c variables between training and control groups. HbA1c (%) value was obtained as a result of the participant's routine blood test.
At the first interview (baseline) and at the second interview 3 months later
Total cholesterol value
Time Frame: At the first interview (baseline) and at the second interview 3 months later
Comparison of total cholesterol variables between training and control groups. Total cholesterol (mg/dl) value was obtained as a result of the participant's routine blood test.
At the first interview (baseline) and at the second interview 3 months later
Low-density lipoprotein value
Time Frame: At the first interview (baseline) and at the second interview 3 months later

Comparison of low-density lipoprotein variables between training and control groups.

Low density lipoprotein (mg/dl) value was obtained as a result of the participant's routine blood test.

At the first interview (baseline) and at the second interview 3 months later
High-density lipoprotein value
Time Frame: At the first interview (baseline) and at the second interview 3 months later

Comparison of high-density lipoprotein variables between training and control groups.

High density lipoprotein (mg/dl) value was obtained as a result of the participant's routine blood test.

At the first interview (baseline) and at the second interview 3 months later
Triglyceride value
Time Frame: At the first interview (baseline) and at the second interview 3 months later
Comparison of triglyceride variables between training and control groups. Triglyceride (mg/dl) value was obtained as a result of the participant's routine blood test.
At the first interview (baseline) and at the second interview 3 months later
Systolic blood pressure value
Time Frame: At the first interview (baseline) and at the second interview 3 months later

Comparison of systolic blood pressure (mmHg) variables between training and control groups.

The tools required for blood pressure measurement were provided by the researcher. The same measurement tools were used in the first interview (pretest) and the second interview (posttest). The participant was allowed to rest for at least 5-10 minutes before the measurement. An aneroid type sphygmomanometer, suitable for adults, was used as a measurement tool. In accordance with the technique recommended in the National Hypertension Treatment and Follow-up Guide, the researcher took measurements twice with an interval of two minutes while the participant was in a sitting position, with his right arm supported at heart level, and the results were recorded by averaging the measurements.

At the first interview (baseline) and at the second interview 3 months later
Diastolic blood pressure value
Time Frame: At the first interview (baseline) and at the second interview 3 months later

Comparison of diastolic blood pressure (mmHg) variables between training and control groups.

The tools required for blood pressure measurement were provided by the researcher. The same measurement tools were used in the first interview (pretest) and the second interview (posttest). The participant was allowed to rest for at least 5-10 minutes before the measurement. An aneroid type sphygmomanometer, suitable for adults, was used as a measurement tool. In accordance with the technique recommended in the National Hypertension Treatment and Follow-up Guide, the researcher took measurements twice with an interval of two minutes while the participant was in a sitting position, with his right arm supported at heart level, and the results were recorded by averaging the measurements.

At the first interview (baseline) and at the second interview 3 months later
Body Mass Index value
Time Frame: At the first interview (baseline) and at the second interview 3 months later
Comparison of body mass index variables between training and control groups. To calculate the body mass index of the participants, they were measured according to the weight and height technique. Participants' BMI was calculated by dividing their weight by the square of their height [BMI: Weight (kg)/height (m2)]. BMI was evaluated in accordance with WHO recommendations.
At the first interview (baseline) and at the second interview 3 months later
Waist circumference value
Time Frame: At the first interview (baseline) and at the second interview 3 months later

Comparison of waist circumference variables between training and control groups.

Waist circumference measurement was made using the measurement technique recommended by WHO. While the participants were standing, the circumference was measured with a tape measure over their underwear, at the midpoint between the lowest rib and the crista iliaca at the end of expiration.

At the first interview (baseline) and at the second interview 3 months later
Numerical distribution of participants' sociodemographic and diabetes-related characteristics
Time Frame: At the first meeting (initial)

The sociodemographic and diabetes-related characteristics of the training and control groups.

Sociodemographic characteristics; Age, gender, marital status, education level, occupation, income level, smoking and alcohol use were evaluated.

Characteristics of diabetes: duration of diabetes, diabetes treatment method, use of other medications, family history of diabetes, frequency of check-ups, hospitalization due to high blood sugar, hospitalization due to hypoglycemia, chronic complications due to diabetes, previous education on diabetes, status other than diabetes the presence of the disease was evaluated.

At the first meeting (initial)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: İlknur METİN AKTEN, PhD,MSc,RN, Kırklareli University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 21, 2022

Primary Completion (Actual)

April 5, 2022

Study Completion (Actual)

August 19, 2022

Study Registration Dates

First Submitted

October 30, 2023

First Submitted That Met QC Criteria

December 11, 2023

First Posted (Actual)

December 20, 2023

Study Record Updates

Last Update Posted (Actual)

December 29, 2023

Last Update Submitted That Met QC Criteria

December 24, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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