Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Allergic Rhinitis
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: pretest-posttest, parallel group, randomized controlled studyMasking: Single (Outcomes Assessor)Primary Purpose: Supportive Care

Participation Requirements

Age
Between 6 years and 12 years
Gender
Both males and females

Description

Allergic rhinitis (AR) is a clinical picture resulting from one or more allergen sensitivities. Seasonal AR develops due to grass, tree and grass pollen. Prennial AR develops due to house dust mite, cockroaches, mold and pets.The prevalence of allergic rhinitis in children ranges from 19.3-50.8%. AR...

Allergic rhinitis (AR) is a clinical picture resulting from one or more allergen sensitivities. Seasonal AR develops due to grass, tree and grass pollen. Prennial AR develops due to house dust mite, cockroaches, mold and pets.The prevalence of allergic rhinitis in children ranges from 19.3-50.8%. AR affects school performance, sleep patterns and quality of life in children.Children spend most of their lives in the home environment, and many studies have shown that AR is associated with the home environment in children. Control measures should be taken in patients' homes to prevent and reduce the symptoms of allergic rhinitis in children. Awareness and education should be provided to families and children about the importance of these measures. This study is a pretest-posttest, parelel group, randomized controlled study study to examine the effect of nursing intervention to regulate the home environment on symptom control and quality of life in children with allergic rhinitis. sample of the study; The effect size was intended to be medium effect size due to the absence of a similar randomized controlled study to determine the quality of life in children with allergic rhinitis. In the study, the number of samples to be included in the study with 0.7 medium effect size, power 80%, alpha reliability level 95%, 26 experiments and 26 controls were calculated as 52 children and their mothers. Considering the 20% loss that may occur in the study, it was decided to include 62 children and their mothers in the study group. Randomized appointments were made in the appointment of 62 children and mothers who were followed up with the diagnosis of allergic rhinitis, who included the criteria for inclusion and exclusion, and who volunteered to participate in the study. Stratified randomization method was used in this study. Stratified randomization method was used in this study. The gender of the children (girls and boys), the age of the children (6-9 years, 10-12 years) and the level of mother education (primary education, high school, university) were determined as prognastic factors for stratification. Randomization was performed in a total of 62 participants, 31 experimental and 31 control groups. Study Group Inclusion Criteria The child is diagnosed with allergic rhinitis, 6-12 age group children and their mothers, The child's sensitivity to at least one of Dermatophagoides pteronyssinus and/or dermatophagoides farinae according to the skin prick test. Although sensitive to at least one of the house dust mites Dermatophagoides pteronyssinus and / or Dermatophagoides farinae according to the child's skin pric test; The child has mold allergy according to the skin prick test, The child is allergic to cockroaches according to the skin prick test, The child has any of the cat and dog allergies according to the skin prick test, The child and his mother live in the city center Volunteering to participate in the research Data Collection Tools; "Mother and Family, Child and Disease, Home Environment Information Form", "Home Environment Assessment Form", "Quality of Life Questionnaire for 6-12 Years Old Children with Allergy in Nose and Eyes (pediatric rinitis quality of life questionnaire PRQLQ)", "Symptom Diary","Humidity and Temperature Measurement "Diary" will be used. Number, percentage, average and standard deviation will be used in the evaluation of the descriptive data obtained from the research; Significance will be evaluated within 95% confidence interval, p <0.05 will be taken. For the implementation of the study, permission was obtained from the ethics committee of Necmettin Erbakan University Meram Medical Faculty, Non-Drug and Medical Device Research Ethics Committee, and work permit was obtained from Necmettin Erbakan University Meram Medical Faculty Hospital Chief Physician. Patients included in the study sample will be informed before the study that the purpose of the study and participation in the study is in line with the principle of volunteering and "Informing and Consent of Volunteers Consent Form" will be signed. implementation of the research The nursing attempt to organize the home environment for the experimental group will take 4 months. During this period, two home visits and two telephone calls will be made. During the first home visit, training will be organized to regulate the home environment, as well as a heat-moisture meter and anti-allergic duvet cover set. There will be two home visits to the control group. During the first home visit, a heat-humidity meter device will be given. Data collection forms will be applied at the beginning and end of the study.training will be organized at the end of the study.

Tracking Information

NCT #
NCT04479085
Collaborators
Not Provided
Investigators
Principal Investigator: Muradiye ALDEM BUDAK Necmettin Erbakan University Study Director: Emine GEÇK?L Necmettin Erbakan University