NCT05437367

Brief Summary

This study will be conducted to investigate the effect of scapular stabilization exercises on scapular muscles strength (serratus anterior, lower fibers of trapezius, rhomboid major and minor), pain intensity level and kyphosis index in different duration of time using daily of smartphone in smartphone users.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
88

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jun 2022

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2022

Completed
17 days until next milestone

First Submitted

Initial submission to the registry

June 18, 2022

Completed
11 days until next milestone

First Posted

Study publicly available on registry

June 29, 2022

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2023

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2023

Completed
Last Updated

June 29, 2022

Status Verified

June 1, 2022

Enrollment Period

1 year

First QC Date

June 18, 2022

Last Update Submit

June 23, 2022

Conditions

Outcome Measures

Primary Outcomes (3)

  • Assessment of change in scapular Muscles strength

    To assess the change in scapular Muscles strength by pull push dynamometer (Newton).

    at baseline and after 4 weeks of intervention

  • Assessment of change in kyphosis Index

    To assess the change in kyphosis Index for thoracic spine pre and post scapular Stabilization exercises for smartphone users by flexible ruler.

    at baseline and after 4 weeks of intervention

  • Assessment of change in pain intensity level

    To assess the change in pain intensity level using visual analog scale (scores) (score 0: means no pain \& score 10: means highest pain)

    at baseline and after 4 weeks of intervention

Study Arms (4)

posture correction exercises group 1

OTHER

Group A (Control group 1): Participants using smartphones more than 4 hours per day will receive posture correction exercises only.

Other: Postural correction exercises

scapular stabilization and postural correction exercises group 1

EXPERIMENTAL

Group B (Experimental group 1): Participants using smartphones more than 4 hours per day will receive scapular stabilization and postural correction exercises.

Other: Scapular Stabilization exercisesOther: Postural correction exercises

posture correction exercises group 2

OTHER

Group C (Control group 2): Participants using smartphones less than 4 hours per day will receive posture correction exercises only.

Other: Postural correction exercises

scapular stabilization and postural correction exercises group 2

EXPERIMENTAL

Group D (Experimental group 2): Participants using smartphones less than 4 hours per day will receive scapular stabilization and postural correction exercises.

Other: Scapular Stabilization exercisesOther: Postural correction exercises

Interventions

Therapeutic exercises

scapular stabilization and postural correction exercises group 1scapular stabilization and postural correction exercises group 2

Therapeutic exercises

posture correction exercises group 1posture correction exercises group 2scapular stabilization and postural correction exercises group 1scapular stabilization and postural correction exercises group 2

Eligibility Criteria

Age17 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may not qualify if:

  • Any pain or limitation (dysfunction) at neck and shoulder.
  • Any congenital abnormalities in either the cervical or the lumbar spine.
  • Previous history of severe surgical procedures.
  • Any history of upper extremity injury within the past year.
  • Visual problems, dizziness and vertigo.
  • Any deformity in the upper extremities or spine.
  • Neurological or systemic disorders.
  • If they had taken any sedative drug or alcohol within the past 48 hours.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cairo University

Dokki, Outpatient Clinic, Faculty of Physical Therapy, 34518, Egypt

RECRUITING

MeSH Terms

Conditions

Muscle WeaknessInternet Addiction Disorder

Condition Hierarchy (Ancestors)

Muscular DiseasesMusculoskeletal DiseasesNeuromuscular ManifestationsNeurologic ManifestationsNervous System DiseasesPathologic ProcessesPathological Conditions, Signs and SymptomsSigns and SymptomsTechnology AddictionBehavior, AddictiveCompulsive BehaviorImpulsive BehaviorBehavior

Study Officials

  • Amira Hussin

    Cairo University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
FACTORIAL
Model Details: Randomized experimental, controlled study (pretest- posttest measurement). Inclusion Criteria
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator

Study Record Dates

First Submitted

June 18, 2022

First Posted

June 29, 2022

Study Start

June 1, 2022

Primary Completion

June 1, 2023

Study Completion

July 1, 2023

Last Updated

June 29, 2022

Record last verified: 2022-06

Locations