Effect of an Audio Instructional Program Regarding Puberty on Self-Concept and Healthy Behaviors of Teenage Girls With Visual Impairment (Teen Audio)

March 22, 2026 updated by: Ashraf Jehad Abuejheisheh, Al-Quds University

Effect of an Audio Instructional Program Regarding Puberty on Self-Concept and Healthy Behaviors of Teenage Girls With Visual Impairment: A Quasi-Experimental Study

Background: Teenage girls, who are a vulnerable group, require special care and attention, particularly when puberty begins. A consistent teaching program about menstruation should be offered to adolescent girls with visual disabilities.

Aim: The goal of this research was to evaluate the effect of an audio instructional program regarding puberty on self-concept and healthy behavior of teenage girls with visual impairment.

Methods: A Quasi-experimental research design. The study was carried out in Al- Nor and Al- Aml schools in Port-Said city & Damietta city, one school in each city. Purposive sampling included 46 visually impaired teenage girls (25) at Port-Said City and (21) at Damietta City. Data collection instruments: Survey for Structured Interviews, Adolescents' Self-concept Short Scale, puberty healthy behavior questionnaire.

Study Overview

Study Type

Interventional

Enrollment (Actual)

46

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 Locations

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

  • Child
  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Age from12-18 year
  • Had signs of puberty and menstruation,
  • Unmarried.
  • Capable to interact.

Exclusion Criteria:

  • Girls who had any verbal disability.
  • Girls who had mental impairment.

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: Prevention
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Audio Puberty Instructional Program for Visually Impaired Adolescent Girls

Single experimental arm including visually impaired adolescent girls who received a structured audio-based puberty educational program. The arm involved three sequential audio instructional sessions delivered in small groups within specialized schools, supported by Braille educational booklets for participants and simplified materials for mothers.

The intervention focused on improving knowledge about puberty, menstrual hygiene and nutrition practices, daily healthy behaviors, and self-concept. Outcomes were evaluated using pre-test, immediate post-test, and three-month follow-up assessments without a control or comparison group.

The intervention was a structured audio-based educational program on puberty specifically designed for visually impaired adolescent girls. It differed from routine school health education by being fully accessible, audio-centered, and supplemented with Braille materials, rather than relying on visual or printed resources.

Key distinguishing features included:

Format: Three prerecorded and researcher-delivered audio instructional sessions in simple Arabic language, tailored to the comprehension level of adolescents with visual impairment.

Content Scope: Comprehensive coverage of pubertal physiological changes, menstrual cycle information, emotional and psychological changes, menstrual hygiene practices, nutrition during menstruation, and daily healthy behaviors.

Accessibility Adaptations: Provision of a Braille-printed educational booklet for each participant and an additional simplified booklet for mothers to reinforce home-based support.

Delivery Method: Small group sessions cond

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Adolescents' Self-concept Short Scale:
Time Frame: up to 3 months

Self-concept of teenage girls regarding puberty development scale will be used. This scale has 30 items in total, broken down into six dimensions: behavior, popularity, happiness, anxiety, physical appearance, and intellectual status. There are five items in each dimension.

Total self -concept / score Total self - / Concept type 75% to 100%. (135-180) degree = Good

50% to less than 75 % (90-135 degree) = Fair

Less than 50%. (<90degree ) = poor

up to 3 months

Collaborators and Investigators

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

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 (Actual)

October 1, 2024

Primary Completion (Actual)

December 31, 2024

Study Completion (Actual)

December 31, 2024

Study Registration Dates

First Submitted

March 16, 2026

First Submitted That Met QC Criteria

March 22, 2026

First Posted (Actual)

March 27, 2026

Study Record Updates

Last Update Posted (Actual)

March 27, 2026

Last Update Submitted That Met QC Criteria

March 22, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Due to sensitivity of data

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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