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Metabolic Control Adolescents Type 1 Diabetes

T

Toros University

Status

Completed

Conditions

13-18 Year
Being Able to Read and Write
HbA1C> 7.5
Diagnosed at Least 6 Months Ago

Treatments

Behavioral: training sessions with peer interactive group

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Purpose of the research; The aim of this study is to examine the effect of education including peer-interactive group support to be given to adolescents diagnosed with Type 1 diabetes with poor glycemic control in the 13-18 age group on metabolic control of adolescents.

Full description

The lack of a certificate program specific to pediatric diabetes nursing of the Ministry of Health in our country and the insufficient number of diabetes education nurses show that the pediatric population is not adequately trained to provide diabetes management. Along with these obstacles, the lack of use of an evidence-based standard education program reveals the need for effective intervention programs that include approaches specific to adolescents, who are a particularly risky group. Peer interaction can be used as an effective approach to increase adolescents' adherence to treatment. Thus, adolescents who isolate themselves are given the opportunity to cope with the disease and to share with other children. It has been determined that there is no study in the literature that includes peer-interactive group support on adolescents with a diagnosis of Type 1 diabetes who have poor glycemic control but have repeated hospitalizations. This situation shows that there is a need for a study to evaluate the effect of educational intervention including peer-interactive group support on repeated hospitalizations in adolescents with Type 1 diabetes.

Enrollment

46 patients

Sex

All

Ages

13 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • be between 13-18 years old
  • Diagnosed at least 6 months ago
  • HbA1C level > 7.5
  • Having repeated hospitalizations at least twice
  • Living in Mersin city center
  • Being able to communicate in Turkish
  • Being able to read and write

Exclusion criteria

    • Using an insulin pump
  • Having a chronic disease other than diabetes,
  • Diseases that affect cognitive functions, hearing and vision impairments

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

46 participants in 2 patient groups

Enterprise Group
Experimental group
Description:
The contents of the research were created according to the Roy Adaptation model. Each session lasted an average of 2 hours. Peer interactive group support sessions were administered to the adolescents in the intervention group, one week apart. There were 7 sessions in total. The sitting arrangement of the training room is designed to allow children to interact with each other . The sessions lasted an average of 90 minutes as two 45-minute sessions. Between sessions, breaks that lasted for about 15 minutes were given and refreshments prepared for individuals with Type 1 diabetes were served during the breaks. During the break, the adolescents were given the opportunity to interact with each other by chatting. Fun exercise and kitchen workshop activities were also organized as interaction sessions in the initiative group.
Treatment:
Behavioral: training sessions with peer interactive group
Control Group
No Intervention group
Description:
Adolescents and their families were informed in the diabetes education room in the pediatric endocrine service of the hospital where the study was conducted, and their written consent was obtained. Within the scope of the pre-test, "Diabetes Adolescent Diagnosis Form", "Diabetes Information Evaluation Form", "Diabetes Management Self-Efficacy Scale in Adolescents with Type 1 Diabetes" and "Child's Attitude towards Own Disease Scale" were applied. Then, individual diabetes education was given by the diabetes education nurse as a hospital routine. Three months after the training, the adolescents were called by phone to the hospital for control, HbA1c follow-up was taken and post-test applications were made.

Trial contacts and locations

1

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Central trial contact

Didem POLAT KÜLCÜ, PhD

Data sourced from clinicaltrials.gov

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