Skip to main content
Clinical Trials/NCT05766215
NCT05766215
Not yet recruiting
Not Applicable

Influence of Nurse-led Therapeutic Patient Education on Glycemic Control and Knowledge of Patients With Type 1 Diabetes Mellitus in Hospital Transition: a Quasi-experimental Trial

Hospitales Universitarios Virgen del Rocío1 site in 1 country13 target enrollmentSeptember 30, 2023
ConditionsNurse's Role

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Nurse's Role
Sponsor
Hospitales Universitarios Virgen del Rocío
Enrollment
13
Locations
1
Primary Endpoint
Height
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

The goal of this interventional quasiexperimental study is to learn about the influence of therapeutic education carried out by nurses in the management and knowledge of patients with T1DM. Participants will be:

Given several therapeutic education sessions. Evaluated using different questionnaires and anthropometric measures.

Detailed Description

The main objective of the study will be to determine the influence of therapeutic education carried out by nurses in the management and knowledge of patients with T1DM who will make a hospital transition. The research design will be a single-blind, nonrandomized, quasi-experimental, single-center, 1-group controlled study . It will be developed at the Center for Diagnosis and Treatment (CDT) of the Virgen del Rocío University Hospital (HUVR), in Seville (Spain). The participant selection process will be carried out considering that only 13 adolescents 17 and 18 years and younger with T1DM, belonging to the reference hospital area, will transit from the Children's Hospital to the Adult Hospital. It is estimated that the study will have a sample of a minimum of n=10, which will be studied over 12 months. Given the existing bibliography about the benefits of this intervention , 1 it is expected that the glycosylated hemoglobin (HbA1c) of patients will be less than 7%, which together with the Self-Management Adherence Questionnaire for Diabetes Treatment (SCI-R. es) 2 represents that patients perform adequate management of their disease. The Survey of Eating Problems in Diabetes Summary Questionnaire (EPAD-R) 3 will be used to assess their eating behavior. An improvement in people's knowledge regarding hypoglycemia is also sought, measured with the Clarke test 4 ; and an improvement in the quality of life, measured with the SF-12 questionnaire 5 and family support with the Apgar test 6 . The therapeutic plan consists of preparing the process prior to discharge from the pediatric center, transferring to the adult hospital with a clinical and educational report and a previously arranged visit to the new unit. The heads of both teams coordinate the structure and the transition process with regular meetings. From the Adult Diabetes Day Hospital, a joint visit is reserved with the endocrinologist and the nurse educator. They are integrated into a 12-month therapeutic care and education program. It consists of four structured phases: 1. Welcome nurse visit, 2. Diabetologic education course adapted to the detected needs, 3. Individualized follow-up through alternating quarterly appointments between nurses and endocrine physician, 4. Evaluation and discharge of the program. At the beginning (baseline visit), at 3 and 12 months the following variables are recorded: 1. Age (years), sex (female/male), T1DM evolution (years). 2. Treatment type (basal-bolus/insulin pump). Sensor usage time (\>80%) 3. Metabolic control: HbA1C (mg/ dL ), Time in Range (TIR), Time Above Range (TAR), Time Below Range (TBR), Coefficient of Variation (CV), Mean Glucose (GMI), weight (Kg), height (cm), BMI (Kg/m 2 ). 4. Perception of quality of life. Test SF-12, of 12 questions. 5. Perception of symptoms of hypoglycemia. Clarke test, 8 questions. 6. Eating behavior, with the EPAD-R test, of 16 questions. 7. Adherence to diabetes treatment. SCI-R.es test. The results analysis plan will be carried out using Microsoft Excel, SPSS or R Commander computer programs , in which the relationships between the descriptive statistics extracted from the screened data will be explored to prevent duplicates. The same digital tools will be used to guarantee the protection of the data and variables collected. This aspect is detailed in the attached informed consent. Regarding the ethical and legal aspects of the study, it is worth mentioning the benefit in disease management, quality of life and general satisfaction that the protocolized follow-up will cause in adolescents. No risk to the psychosocial integrity of the population involved in the study has been detected. The necessary facilities will be the Education Classroom of the HUVR Diabetes Day Hospital, computer support through 2 computers, paper resources for the questionnaires, 2 nurses and 1 endocrinologist will be necessary as human resources. The authors declare the absence of funding or conflict of interest for the development of the research.

Registry
clinicaltrials.gov
Start Date
September 30, 2023
End Date
December 22, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Hospitales Universitarios Virgen del Rocío
Responsible Party
Principal Investigator
Principal Investigator

Pilar Santa Cruz Álvarez

Enfermera de Práctica Avanzada (EPA)

Hospitales Universitarios Virgen del Rocío

Eligibility Criteria

Inclusion Criteria

  • Age 17 years.

Exclusion Criteria

  • Unable to give informed consent.

Outcomes

Primary Outcomes

Height

Time Frame: 12 months

cm

Glycated hemoglobin.

Time Frame: 12 months

HbA1c

Coefficient of variation

Time Frame: 12 months

CV

Time below range

Time Frame: 12 months

TBR

Glucose Management Indicator

Time Frame: 12 months

GMI

Weight

Time Frame: 12 months

Kg

Body Mass Index

Time Frame: 12 months

BMI

Time above range

Time Frame: 12 months

TAR

Time in Range

Time Frame: 12 months

TIR

Secondary Outcomes

  • Adherence to diabetes treatment(12 months)
  • Perception of symptoms of hypoglycemia(12 months)
  • Eating behavior,(12 months)
  • Perception of quality of life.(12 months)

Study Sites (1)

Loading locations...

Similar Trials