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Clinical Trials/NCT04733612
NCT04733612
Completed
Not Applicable

Effects of Short-Message Notifications on Medication Adherence, Physical Activity and Fasting Blood Glucose Control and Correlation of These With the Health-Related Quality of Life in Mid-aged Diabetic Patients

Istanbul University0 sites125 target enrollmentJune 30, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Type2 Diabetes Mellitus
Sponsor
Istanbul University
Enrollment
125
Primary Endpoint
Fasting blood glucose
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The objective of our study was to assess awareness-raising of medication adherence (MA), physical activity (PA), fasting blood glucose (FBG), and glycated hemoglobin A (HbA1c) values by providing information on diabetes via short message (SMS) technology.

Detailed Description

The study investigates T2DM patients who have not had surgery or cardiac event in the last 3 months, between the ages of 40 and 64 years, with T2DM diagnosis between the last 1 and 10 years and oral antidiabetic therapy for at least 1 The study design is a single-blinded randomized, controlled study, and was conducted in the Diabetes Polyclinic of the Istanbul University Medical Faculty Hospital. Patients randomly assigned to the intervention group, in addition to traditional treatment received three to four informative SMS messages per week during the 6-month period, while the control group was followed in accordance with the traditional treatment schedule.

Registry
clinicaltrials.gov
Start Date
June 30, 2016
End Date
February 26, 2018
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Bernard Tahirbegolli

Principal Investigator

Istanbul University

Eligibility Criteria

Inclusion Criteria

  • Clinical diagnosis of Type 2 Diabetes Mellitus (T2DM) between the last 1 and 10 years
  • Being aged between 40 and 64 years old,
  • Is treated for a minimum of 1 year with at least one oral antidiabetic drug.

Exclusion Criteria

  • Clinical diagnosis of T2DM for less than 1 year or more than 10 years.
  • Those who have had surgery or a cardiac event in the last 3 months or during the investigation.
  • Those under 40 and over 64 years of age.
  • Patients with T2DM that have not been treated with oral antidiabetic medication.
  • Volunteers who once did not participate in the control examinations in both groups were excluded from the evaluation.

Outcomes

Primary Outcomes

Fasting blood glucose

Time Frame: Beginning

After 8 hours of fasting in the morning, venous whole blood samples were taken to yellow capped tubes for fasting blood glucose (mmol/dL).

Change from Baseline Fasting blood glucose at 3 months

Time Frame: 3 months after beginning

After 8 hours of fasting in the morning, venous whole blood samples were taken to yellow capped tubes for fasting blood glucose (mmol/dL).

Glycated hemoglobin A (HbA1c)

Time Frame: Beginning

In the HbA1c evaluation (%), after 8 hours of fasting by volunteers, venous whole blood samples were taken in purple tubes (EDTA) between 08:00 and 10:00 a.m. and evaluated by the HPLC method.

Change from Baseline Physical Activity at 3 months

Time Frame: 3 months from beginning

The International Physical Activity Questionnaire (IPAQ) was used to evaluate the physical activity level of the participants at at 3 months after the beginning of the study. This measure assesses the types of intensity of physical activity and sitting time that people do as part of their daily lives are considered to estimate total physical activity in MET-min/week and time spent sitting. The higher scores mean a better outcome.

Change from Baseline Drug Adherence at 6 months

Time Frame: 6 months after beginning

The Morisky Medication Adherence Scale (MMAS-8) was used to assess the compliance of patients with drug treatment. If the patient scores higher on the scale, they will be assessed as more adherent. If they score lower on the scale, they are presumed to be struggling with non-adherence.

Change from Baseline Quality of Life Assessed by SF-36v2 at 3 months

Time Frame: 3 months after beginning

The Short-Form Health Survey (SF-36v2) is used to asses the quality of life of volunteers'. It has 36 items grouped in 8 dimensions: physical functioning, physical and emotional limitations, social functioning, bodily pain, general and mental health. The higher scores mean a better outcome.

Change from Baseline of Glycated hemoglobin A (HbA1c) at 3 months

Time Frame: 3 months after beginning

In the HbA1c evaluation (%), after 8 hours of fasting by volunteers, venous whole blood samples were taken in purple tubes (EDTA) between 08:00 and 10:00 a.m. and evaluated by the HPLC method

Physical Activity level

Time Frame: Beginning

The International Physical Activity Questionnaire (IPAQ) was used to evaluate the physical activity level of the participants at the beginning of the study. This measure assesses the types of intensity of physical activity and sitting time that people do as part of their daily lives are considered to estimate total physical activity in MET-min/week and time spent sitting. The higher scores mean a better outcome.

Change from Baseline Fasting blood glucose at 6 months

Time Frame: 6 months after beginning

After 8 hours of fasting in the morning, venous whole blood samples were taken to yellow capped tubes for fasting blood glucose (mmol/dL).

Change from Baseline of Glycated hemoglobin A (HbA1c) at 6 months

Time Frame: 6 months after beginning

In the HbA1c evaluation (%), after 8 hours of fasting by volunteers, venous whole blood samples were taken in purple tubes (EDTA) between 08:00 and 10:00 a.m. and evaluated by the HPLC method

Change from Baseline Physical Activity at 6 months

Time Frame: 6 months from beginning

The International Physical Activity Questionnaire (IPAQ) was used to evaluate the change in physical activity level of the participants at at 6 months after the beginning of the study. This measure assesses the types of intensity of physical activity and sitting time that people do as part of their daily lives are considered to estimate total physical activity in MET-min/week and time spent sitting. The higher scores mean a better outcome.

Drug Adherence

Time Frame: Beginning

The Morisky Medication Adherence Scale (MMAS-8) was used to assess the compliance of patients with drug treatment. If the patient scores higher on the scale, they will be assessed as more adherent. If they score lower on the scale, they are presumed to be struggling with non-adherence.

Change from Baseline Drug Adherence at 3 months

Time Frame: 3 months after beginning

The Morisky Medication Adherence Scale was used to assess the compliance of patients with drug treatment. If the patient scores higher on the scale, they will be assessed as more adherent. If they score lower on the scale, they are presumed to be struggling with non-adherence.

Quality of Life Assessed by SF-36v2

Time Frame: Beginning

The Short-Form Health Survey (SF-36v2) is used to asses the quality of life of volunteers'. It has 36 items grouped in 8 dimensions: physical functioning, physical and emotional limitations, social functioning, bodily pain, general and mental health. The higher scores mean a better outcome.

Change from Baseline Quality of Life Assessed by SF-36v2 at 6 months

Time Frame: 6 months after beginning

The Short-Form Health Survey (SF-36v2) is used to asses the quality of life of volunteers'. It has 36 items grouped in 8 dimensions: physical functioning, physical and emotional limitations, social functioning, bodily pain, general and mental health. The higher scores mean a better outcome.

Secondary Outcomes

  • Baseline heart rate(Beginning)
  • Baseline blood pressure(Beginning)
  • Change from Baseline blood pressure at 3 months(3 months after beginning)
  • Change from Baseline heart rate at 3 months(3 Months After Beginning)
  • Change from Baseline Body Mass Index at 6 months(6 months after Beginning)
  • Change from Baseline blood pressure at 6 months(6 months after beginning)
  • Change from Baseline heart rate at 6 months(6 Months After Beginning)
  • Baseline body fat ratios(Beginning)
  • Baseline Body Mass Index(Beginning)
  • Change from Baseline waist/hip ratio at 3 Months(3 Months after Beginning)
  • Change from Baseline Body Mass Index at 3 months(3 months after Beginning)
  • Change from Baseline Diet and Nutritional Habits at 6 months(6 Months after Beginning)
  • Change from Baseline Body Fat Ratios at 3 Months(3 Months After Beginning)
  • Baseline Energy Intake(Beginning)
  • Change from Baseline Energy Intake at 3 months(3 months after Beginning)
  • Change from Baseline Body Fat Ratios at 6 Months(6 Months After Beginning)
  • Baseline waist/hip ratio(Beginning)
  • Baseline Diet and Nutritional Habits(Beginning)
  • Change from Baseline Diet and Nutritional Habits at 3 months(3 Months after Beginning)
  • Change from Baseline Energy Intake at 6 months(6 months after Beginning)

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