Mechanical Posture Changes in Adolescent Female at Public Schools Compared to International Schools

January 26, 2021 updated by: HAhmed, Cairo University
The aim of this study is to determine different mechanical posture changes in adolescent females at public schools compared to international schools.

Study Overview

Status

Completed

Conditions

Detailed Description

Two hundred adolescent female subjects at public schools and in this study. All subjects will be recruited from different schools. 1-Group A: it will be consists of 200 adolescent female from public schools, will be evaluated by Posture screen mobile, (BackPEI) questionnaire , VISUAL ANALOG SCALE (VAS)and Depression Anxiety Stress Scales-21(DASS-21).

2- Group B: it will be consists of 200 adolescent female from international schools, will be evaluated by Posture screen mobile, (BackPEI) questionnaire , VISUAL ANALOG SCALE (VAS) and Depression Anxiety Stress Scales-21(DASS-21).

Study Type

Observational

Enrollment (Actual)

200

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

      • Cairo, Egypt, 14788
        • Cairo University

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

13 years to 17 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

Adolescent female at schools.

Description

Inclusion Criteria:

  1. Adolescent female at schools.
  2. Their age will be ranged from 13 to 17 years.
  3. BMI more than 20.
  4. Initiated menstrual cycle.

Exclusion Criteria:

  1. Asthma and chronic respiratory disease.
  2. History of upper and lower limb injury.
  3. Under weight subjects.
  4. Females with congenital spinal deformities.
  5. Diabetes, cardiopulmonary diseases and any physical impairment that prevent following the study program.

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
A(public school)

it will be consists of 200 adolescent female from public schools, their age will be ranged from 13 to 17 years, initiated menstrual cycle and BMI more than 20.mechanical posture changes will be evaluated by Posture screen mobile. back pain and life style will be evaluated by (BackPEI) questionnaire.

pain will be evaluated by VISUAL ANALOG SCALE(VAS) .stress will be evaluated by Depression Anxiety Stress Scales-21(DASS-21).

evaluated by Posture screen mobile, (BackPEI) questionnaire , VISUAL ANALOG SCALE (VAS), Depression Anxiety Stress Scales-21(DASS-21).
B(international school)
it will be consists of 200 adolescent female from international schools their age will be ranged from 13 to 17 years, initiated menstrual cycle and BMI more than 20.mechanical posture changes will be evaluated by Posture screen mobile. back pain and life style will be evaluated by (BackPEI) questionnaire .pain will be evaluated by VISUAL ANALOG SCALE (VAS).stress will be evaluated by Depression Anxiety Stress Scales-21(DASS-21).
evaluated by Posture screen mobile, (BackPEI) questionnaire , VISUAL ANALOG SCALE (VAS), Depression Anxiety Stress Scales-21(DASS-21).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
posture deviations
Time Frame: up to 6months
Lateral shift from the midline and tilting through frontal and lateral views.
up to 6months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
weight
Time Frame: up to 6months
Anthropometric measurement measure by kilogram (kg).
up to 6months
height
Time Frame: up to 6months
Anthropometric measurement measure by centimeter (cm).
up to 6months
body mass index (BMI).
Time Frame: up to 6 months
calculated by dividing weight (in kilograms) by your height (in metres squared). kg/m2
up to 6 months
Back Pain and Body Posture Evaluation Instrument (BackPEI) questionnaire
Time Frame: up to 6months
Back Pain and Body Posture Evaluation Instrument .The BackPEI questionnaire consists of 21 closed questions, which address the occurrence, frequency and intensity of pain, as well as questions on demographic (age, gender) and behavioral factors (level of exercise, competitive or non-competitive practice of exercise, daily hours watching television and using the computer, number of daily hours of sleep, reading and/or studying in bed, and postures in activities of daily living.
up to 6months
Visual analogue scale
Time Frame: up to 6months
Numerical pain rating scale (minimum score 0 and maximum score 10) ,Instruct the patient to choose a number from 0 to 10 that best describes their current pain. 0 would mean "no pain" and 10 would mean "worst possible pain.
up to 6months
Depression Anxiety Stress Scales-21(DASS-21)
Time Frame: up to 6months
Was developed to provide a self-report measure of anxiety, depression and stress signals. During the development process.Questionnaire consists of 21 questions,seven questions for depression ,seven for anxiety and seven for stress assessment.The responses are given on a 4-point Likert scale, ranging from zero if "I strongly disagree" to 3 if "I totally agree". Overall scores for the three constructs are calculated as the sum of scores for the relevant seven items multiplied by two. Ranges of scores correspond to levels of symptoms, ranging from "normal" to "extremely serious
up to 6months

Collaborators and Investigators

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

Investigators

  • Study Director: fahema me okeel, phD, Cairo University

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)

March 1, 2019

Primary Completion (Actual)

July 17, 2020

Study Completion (Actual)

August 1, 2020

Study Registration Dates

First Submitted

January 10, 2019

First Submitted That Met QC Criteria

February 18, 2019

First Posted (Actual)

February 20, 2019

Study Record Updates

Last Update Posted (Actual)

January 27, 2021

Last Update Submitted That Met QC Criteria

January 26, 2021

Last Verified

January 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • MPCAF

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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