- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03847259
Mechanical Posture Changes in Adolescent Female at Public Schools Compared to International Schools
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Cairo, Egypt, 14788
- Cairo University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adolescent female at schools.
- Their age will be ranged from 13 to 17 years.
- BMI more than 20.
- Initiated menstrual cycle.
Exclusion Criteria:
- Asthma and chronic respiratory disease.
- History of upper and lower limb injury.
- Under weight subjects.
- Females with congenital spinal deformities.
- Diabetes, cardiopulmonary diseases and any physical impairment that prevent following the study program.
Study Plan
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
Sponsor
Investigators
- Study Director: fahema me okeel, phD, Cairo University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Other Study ID Numbers
- MPCAF
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.
Clinical Trials on Adolescent Behavior
-
World Health OrganizationLondon School of Hygiene and Tropical Medicine; University of Ghana; Biomedical... and other collaboratorsRecruitingHealth-Related Behavior | Adolescent Behavior | Adolescent Development | Health Care Seeking BehaviorGhana, Tanzania, Zimbabwe
-
University of CoimbraRecruitingAdolescent Behavior | Adolescent - Emotional ProblemPortugal
-
University of North Carolina, Chapel HillNot yet recruitingAdolescent BehaviorUnited States
-
Seattle Children's HospitalRecruiting
-
Karabuk UniversityCompleted
-
Child TrendsUniversity of California, San Francisco; Power to DecideRecruiting
-
Centerstone Research InstituteActive, not recruitingRisk Reduction | Adolescent Behavior | Adolescent Problem BehaviorUnited States
-
The University of Texas Medical Branch, GalvestonEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsCompleted
-
Child TrendsUniversity of Maryland; Identity, Inc.Completed
-
Stanford UniversityRecruitingAdolescent BehaviorUnited States
Clinical Trials on mechanical posture changes
-
Rambam Health Care CampusUnknownHeart Rate Determination
-
Alejandro Muñoz LópezUnknown
-
Hospital Moinhos de VentoHospital Ernesto DornellesTerminated
-
Wake Forest UniversityNational Heart, Lung, and Blood Institute (NHLBI)Completed
-
Benha UniversityRecruitingCOVID-19 | Tachycardia | Cardiac Arrhythmia | Stress Reaction | Accommodation SpasmEgypt
-
Arizona State UniversityCompletedHypertension | Diabetes | Sleep
-
Amasya UniversityNot yet recruiting
-
İlke KARA, PTDokuz Eylul UniversityCompletedQuality of Life | Physical InactivityTurkey
-
Cukurova UniversityCompletedHemophilia | Postural; Defect | Muscle DisorderTurkey
-
Akdeniz UniversityNot yet recruitingWork-Related Musculoskeletal Disorders | Ergonomic Risk Exposure