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The Effect of Individualized Nursing Interventions on Glycemic Variability and Self-Management in Type 2 Diabetes

The Effect of Individualized Nursing Interventions for Blood Glucose Variability Risk on Nursing Outcomes and Self-Management of Diabetes in Patients With Type 2 Diabetes

Source: ClinicalTrials.gov · Last updated 28 Oct 2026

Brief summary (registry, in English)

Type 2 diabetes is a chronic disease with an increasing prevalence worldwide and in our country. In managing type 2 diabetes, the primary goal in the nursing process is to ensure blood glucose stability. In this regard, it is essential to provide individualized nursing interventions and diabetes management education to individuals. The Comprehensive Self-Management of Diabetes Scale can be used to determine individuals' level of diabetes management. Implementing systematic nursing interventions to maintain blood glucose stability and evaluating their impact on nursing outcomes and diabetes management are crucial. Although the NANDA, NIC, and NOC (NNN) system is used for this purpose, research in this area remains limited. There is a need for studies investigating the effects of individualized nursing interventions based on the NNN system on nursing outcomes and comprehensive self-management of diabetes in patients with type 2 diabetes who are at risk of blood glucose variability. This study is planned as a randomized controlled trial with repeated measurements. The topic is original in terms of implementing individualized nursing interventions, providing education, and monitoring patients according to the NNN system to address the risk of blood glucose variability in patients with type 2 diabetes, as well as evaluating its impact on nursing outcomes and comprehensive self-management of diabetes. Another unique aspect of the study is that the effects of the interventions will also be assessed through laboratory results, including fasting blood glucose (FBG), postprandial blood glucose (PBG), HbA1c, height, weight, waist circumference, blood pressure, and pulse measurements. This research aims to improve glycemic control, prevent potential complications of the disease, ensure patient safety, enhance the quality and satisfaction of nursing care, reduce additional treatment costs, and decrease diabetes-related morbidity and mortality. If this study yields positive results, it will contribute to the widespread implementation of individualized nursing interventions using the NNN system to manage blood glucose variability risk, reduce diabetes-related health problems, ensure patient safety, and lower additional treatment costs. Furthermore, it is expected to guide clinical nurses, nurse researchers, and nurse managers in caring for individuals with type 2 diabetes, improve care quality and satisfaction, and support the planning of in-service training programs. From a healthcare institution perspective, it is anticipated to help reduce additional financial burdens and enhance care quality.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
72 (estimated)
First submitted
18 Apr 2025
Start date
Dec 2026
Primary completion date
Dec 2027
Lead sponsor
Ataturk University
NCT number
NCT06973395

What you commit to

  • Study type: Interventional
  • Planned participants: 72
  • From Dec 2026 to the primary completion date, Dec 2027
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Individuals receiving insulin treatment
  • Individuals using steroid treatment will not be included in the study.

Other illness

  • Individuals with liver and kidney failure, myocardial infarction, cerebrovascular accident and cancer

Who the study is looking for

  • Including the data of those aged 18-65,
  • Those receiving oral antidiabetic treatment,
  • Those who can use a smartphone and have internet access,
  • Those who know how to write, read and speak Turkish,
  • Those who do not have communication skills,
  • Those who do not have a mental illness and are on psychiatric medication.

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ataturk University Institute of Health Sciences
Coordinator of this site? Confirm its status
ErzurumTurkey (Türkiye)Unknown status
Atatürk University
Coordinator of this site? Confirm its status
ErzurumTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.