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Mobile Health Application of Screening and Early Intervention for Prediabetic Patient at Primary Health Cares Setting

Not Applicable
Conditions
Prediabetic State
PreDiabetes
Interventions
Device: Mobile health apps
Other: Standard care
Registration Number
NCT04979559
Lead Sponsor
Gadjah Mada University
Brief Summary

Background: Preventing type-2 diabetes mellitus begins with early screening and intervention of prediabetic participants. Until now, prediabetes screening and early intervention have not been optimal. The rapid advancement of technology, as well as its increased use, may provide an opportunity to improve the quality and cost of healthcare services. It is quite practicable to investigate and implement a valid, practical and easy-to-use mobile health application for participants and health staffs in screening and early intervention of prediabetes participants at primary health cares setting. This protocol aimed to identify and develop a valid, practical, and easy-to-use mobile health application for screening and early intervention of prediabetes participants at primary health cares.

Methods: This protocol was prepared in accordance with the Standard Protocol Items: Recommendations for Interventional Trials 2013 statement. This is a mixed-methods study with sequential exploratory approach. This project will begin with in-depth interview to gather qualitative information regarding mobile health application necessity for prediabetes participants at the primary health cares. The impact of the usage will be studied quantitatively using randomized controlled trial. Prediabetic participants and primary health cares staffs at Yogyakarta province will be the research subjects. The collected findings will be examined based on the type of the data.

Discussion: The proposed research aimed to obtain information and trial results regarding mobile health application usage for prediabetes participants screening and early intervention at primary health cares setting.

Detailed Description

The goal of this study is to create a mobile health application for prediabetes patients that included screening and early intervention in Primary Health Cares (PHCs) setting. More specifically, the objectives are as follows:

1. To portray regular prediabetes screening and early intervention practice in PHCs.

2. To assess prediabetes screening and early intervention data necessity for mobile health application model at PHCs.

3. To assess the feasibility of mobile health application usage for screening and early intervention of prediabetes patients at PHCs.

4. To assess internal and external factors that influence the intention-to-use, easiness, and usefulness of mobile health applications for prediabetes patients and health staff.

5. To assess the impact of early intervention using mobile health applications on prediabetes patients.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
350
Inclusion Criteria
  • diagnosed as the prediabetic state using American Diabetes Association (ADA) criteria
  • have no previous diagnosis of type 2 diabetes or history of taking anti-hyperglycemic drugs
  • have access to and able to use a personal smartphone
  • willing to undertake study activities and written informed consent
Exclusion Criteria
  • severe medical condition
  • disability to perform physical activity

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
mHealth appsMobile health appsThe participants in this arm will receive information regarding mobile health applications used for screening and early intervention of the prediabetic states.
Standard careStandard careThe participant in this arm will receive regular practice or standard care of screening and early intervention of prediabetic state.
Primary Outcome Measures
NameTimeMethod
Body weight mean change from baselineat baseline and after intervention at 12-weeks

Participants' body weight measured by scales using kilograms (kg) measurement unit

Waist circumference mean change from baselineat baseline and after intervention at 12-weeks

Participants' waist circumference measured using measuring tape in centimeter (cm) measurement unit

Fasting blood glucose mean change from baselineat baseline and after intervention at 12-weeks

Participants' fasting blood glucose measured from vein blood in milligram per deciliter (mg/dL) measurement unit

Hemoglobin A1c mean change from baselineat baseline and after intervention at 12-weeks

Participants' Hemoglobin A1c measured from vein blood in percent

Oral glucose tolerance test mean change from baselineat baseline and after intervention at 12-weeks

Participants' oral glucose tolerance test measured from vein blood in milligram per deciliter (mg/dL) measurement unit

Secondary Outcome Measures
NameTimeMethod
Area under the curve of screening instrument compared to American Diabetes Association criteriaimmediately after the intervention begin

screening accuracy of the instrument reported using graph

Sensitivity value of screening instrument compared to American Diabetes Association criteriaimmediately after the intervention begin

Sensitivity value of the instrument calculated using formula derived from 2x2 tables of diagnostic test

Specificity value of screening instrument compared to American Diabetes Association criteriaimmediately after the intervention begin

Specificity value of the instrument calculated using formula derived from 2x2 tables of diagnostic test

Positive predictive value of screening instrument compared to American Diabetes Association criteriaimmediately after the intervention begin

Positive predictive value of the instrument calculated using formula derived from 2x2 tables of diagnostic test

Negative predictive value of screening instrument compared to American Diabetes Association criteriaimmediately after the intervention begin

Negative predictive value of the instrument calculated using formula derived from 2x2 tables of diagnostic test

Accuracy value of screening instrument compared to American Diabetes Association criteriaimmediately after the intervention begin

Accuracy predictive value of the instrument calculated using formula derived from 2x2 tables of diagnostic test

Likelihood ratio of screening instrument compared to American Diabetes Association criteriaimmediately after the intervention begin

Likelihood ratio of the instrument calculated using formula derived from 2x2 tables of diagnostic test

Trial Locations

Locations (1)

Kalasan PHC

🇮🇩

Sleman, Yogyakarta, Indonesia

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