Effects of Web-Based Adolescent Health Promotion Program in Hearing Impaired Adolescents (ASGE-FABES)
Effects of Web-Based Adolescent Health Promotion Program on Physical Activity, Nutrition and Mental Health in Hearing Impaired Adolescents
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Purpose of the research; To evaluate the effect and applicability of the Web-Based Adolescent Health Promotion program, which includes multiple health behavior initiatives, on physical activity, nutrition, and stress management of hearing impaired adolescents in making healthy choices, assuming their own health responsibilities and acquiring healthy lifestyle behaviors.
Materials and methods; The research is a full experimental study with pretest-posttest control group, repeated measurement design, random groups.
Research sample; A total of 70 hearing-impaired adolescents aged 12-18, studying at Abdurrahman Gazi Sağlar Primary School, Van Special Education Vocational High School and Duyus Special Education and Rehabilitation Center affiliated to the Ministry of National Education in the city center of Van.
The data of the research; "Sociodemographic Characteristics Information Form", "Body Mass Index (BMI)", "Adolescent Nutrition Information Scale", "Adolescent Physical Activity Information Scale", "Adolescent Lifestyle Scale", "Adolescent Healthy Lifestyle Choices Scale", "Renewed Child" Anxiety and Depression Scale", "Daily Food Consumption Form", "Beverage Consumption Form", "Pedometer" were collected.
In the study; descriptive statistics will be evaluated with mean, standard deviation, percentage and frequency analysis. Comparisons between groups will be analyzed using Pearson's chi-square, Student's t-test, Mann Whitney-U test, Kruskal Wallis test, analysis of variance and Cohen's d effect size.
The results of this study;
- Physical Variables: Body Mass Index (BMI) and Weight
- Behavioral Variables: Weekly average number of steps and change, fruit and vegetable consumption amount, amount of water consumed, amount of sugary and acidic beverages consumed, "Adolescent Lifestyle" scale score average, "Adolescent" Lifestyle Choices scale score average,
- Cognitive Variables: "Adolescent Nutrition Knowledge" scale mean score, "Adolescent Physical Activity Knowledge" scale mean score, "Regenerated Child Anxiety and Depression" scale mean score will be evaluated.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: HAKAN ORAKCI, Phd Student
- Phone Number: +905053878162
- Email: hakanorakci@yyu.edu.tr
Study Locations
-
-
Avcılar
-
İstanbul, Avcılar, Turkey, 34320
- Istanbul University - Cerrahpasa
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Hearing impairment,
- In the 12-18 age group,
- Ability to access communication tools such as computers, tablets and smartphones and use the internet with these tools,
- Able to communicate in visual, sign language and written,
- Does not have a physical condition or disease that may prevent exercise,
- Volunteer to participate in the research,
- Permitted to participate in the research by their parents.
Exclusion Criteria:
- who want to withdraw from the research
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: (Intervention group) Hearing impaired adolescent experimental group
Hearing Impaired Adolescent Group implemented Web-Based Adolescent Health Promotion Education Program
|
Web Based Adolescent Health Promotion Education Program
Other Names:
|
|
No Intervention: (Control group) Hearing impaired adolescent control Group
Hearing Impaired Adolescent Group that did not apply Web-Based Adolescent Health Promotion Education Program
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Physical Variables:
Time Frame: 9 months
|
Body Mass Index (BMI- kg/m^2) and Weight (kg)
|
9 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Behavioral Variables:
Time Frame: 9 months
|
The mean score of "Adolescent Lifestyle Scale" is used for behavioral change;
|
9 months
|
|
Cognitive Variables 1:
Time Frame: 9 months
|
The mean score of "Adolescent Nutrition Knowledge Scale" will be evaluated. Scoring
|
9 months
|
|
Cognitive Variables 2:
Time Frame: 9 months
|
The mean score of "Adolescent Physical Activity Knowledge Scale" will be evaluated. Scoring
|
9 months
|
|
Cognitive Variables 3:
Time Frame: 9 months
|
The mean score of "Regenerated Child Anxiety and Depression Scale" will be evaluated. The RCADS consists of 47 items developed to measure DSM-IV based symptoms of anxiety disorders and depression in children and adolescents. The subscales correspond to SAD (7 items), SP (9 items), GAD (6 items), PD (9 items), OCD (6 items), and MDD (10 items). It is scored on a 4-point scale (0 =never, 1 = sometimes, 2 = often, and 3 = always). |
9 months
|
Collaborators and Investigators
Investigators
- Study Director: AYSUN ARDIÇ, Assoc. Prof., Istanbul University - Cerrahpasa (IUC)
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HAKAN ORAKCI PHD THESIS
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.