ASGE-FABES: Effects of Web-Based Adolescent Health Promotion Program in Hearing Impaired Adolescents

Sponsor
Istanbul University-Cerrahpasa (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05329207
Collaborator
(none)
70
1
2
7
10

Study Details

Study Description

Brief Summary

Our research is to evaluate the effect and applicability of the adolescent health promotion program, which includes multiple behavioral interventions, on physical activity, nutrition and mental health of hearing impaired adolescents living in the community.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Experimental group
N/A

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 Design

Study Type:
Interventional
Anticipated Enrollment :
70 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
The study was in the design type with pretest-posttest control group, repeated measures in randomized groups.The study was in the design type with pretest-posttest control group, repeated measures in randomized groups.
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Effects of Web-Based Adolescent Health Promotion Program on Physical Activity, Nutrition and Mental Health in Hearing Impaired Adolescents
Anticipated Study Start Date :
Apr 18, 2022
Anticipated Primary Completion Date :
Oct 18, 2022
Anticipated Study Completion Date :
Nov 18, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: (Intervention group) Hearing impaired adolescent experimental group

Hearing Impaired Adolescent Group implemented Web-Based Adolescent Health Promotion Education Program

Behavioral: Experimental group
Web Based Adolescent Health Promotion Education Program
Other Names:
  • ASGE-FABES
  • No Intervention: (Control group) Hearing impaired adolescent control Group

    Hearing Impaired Adolescent Group that did not apply Web-Based Adolescent Health Promotion Education Program

    Outcome Measures

    Primary Outcome Measures

    1. Physical Variables: [9 months]

      Body Mass Index (BMI- kg/m^2) and Weight (kg)

    Secondary Outcome Measures

    1. Behavioral Variables: [9 months]

      The mean score of "Adolescent Lifestyle Scale" is used for behavioral change; The scale requires a 4-point Likert-type response for each item. 1 for "Never", 2 for "Sometimes", 3 for "Often" and 4 for "Always" The maximum score obtained from the scale is 160 and the minimum score is 40. The scale does not have a cut-off point, as the score increases, the level of positive health behavior increases

    2. Cognitive Variables 1: [9 months]

      The mean score of "Adolescent Nutrition Knowledge Scale" will be evaluated. Scoring Highlighted answer is correct Recode items If answer don't know (2), recode as no (0) If answer is correct, recode as (1) If answer is incorrect, recode as (0) After recoding, sum items 1-12 Summed total will reflect the number of items answered correctly.

    3. Cognitive Variables 2: [9 months]

      The mean score of "Adolescent Physical Activity Knowledge Scale" will be evaluated. Scoring Highlighted answer is correct Recode items If answer don't know (2), recode as no (0) If answer is correct, recode as (1) If answer is incorrect, recode as (0) After recoding, sum items 1-12 Summed total will reflect the number of items answered correctly.

    4. Cognitive Variables 3: [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).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    12 Years to 18 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Istanbul University - Cerrahpasa İstanbul Avcılar Turkey 34320

    Sponsors and Collaborators

    • Istanbul University-Cerrahpasa

    Investigators

    • Study Director: AYSUN ARDIÇ, Assoc. Prof., Istanbul University-Cerrahpasa

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Hakan ORAKCI, PhD Candidate, Istanbul University-Cerrahpasa
    ClinicalTrials.gov Identifier:
    NCT05329207
    Other Study ID Numbers:
    • HAKAN ORAKCI PHD THESIS
    First Posted:
    Apr 14, 2022
    Last Update Posted:
    Apr 14, 2022
    Last Verified:
    Apr 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Hakan ORAKCI, PhD Candidate, Istanbul University-Cerrahpasa
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 14, 2022