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

April 8, 2022 updated by: Hakan ORAKCI, Istanbul University - Cerrahpasa (IUC)

Effects of Web-Based Adolescent Health Promotion Program on Physical Activity, Nutrition and Mental Health in Hearing Impaired Adolescents

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.

Study Overview

Status

Not yet recruiting

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

Interventional

Enrollment (Anticipated)

70

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Avcılar
      • İstanbul, Avcılar, Turkey, 34320
        • Istanbul University - Cerrahpasa

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

12 years to 18 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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:
  • 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

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;

  • 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
9 months
Cognitive Variables 1:
Time Frame: 9 months

The mean score of "Adolescent Nutrition Knowledge Scale" will be evaluated.

Scoring

  1. Highlighted answer is correct
  2. Recode items

    1. If answer don't know (2), recode as no (0)
    2. If answer is correct, recode as (1)
    3. If answer is incorrect, recode as (0)
  3. After recoding, sum items 1-12
  4. Summed total will reflect the number of items answered correctly.
9 months
Cognitive Variables 2:
Time Frame: 9 months

The mean score of "Adolescent Physical Activity Knowledge Scale" will be evaluated.

Scoring

  1. Highlighted answer is correct
  2. Recode items

    1. If answer don't know (2), recode as no (0)
    2. If answer is correct, recode as (1)
    3. If answer is incorrect, recode as (0)
  3. After recoding, sum items 1-12
  4. Summed total will reflect the number of items answered correctly.
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

This is where you will find people and organizations involved with this study.

Investigators

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

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

April 18, 2022

Primary Completion (Anticipated)

October 18, 2022

Study Completion (Anticipated)

November 18, 2022

Study Registration Dates

First Submitted

January 19, 2022

First Submitted That Met QC Criteria

April 8, 2022

First Posted (Actual)

April 14, 2022

Study Record Updates

Last Update Posted (Actual)

April 14, 2022

Last Update Submitted That Met QC Criteria

April 8, 2022

Last Verified

April 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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.

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