NCT06416917

Unknown

Glenohumeral Internal Rotation Deficit Among Professional At...

Cairo University Source

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Other study identifiers

Sponsor study identifier

prevalence of GIRD

Study Type

observational

Estimated enrollment

70

Locations

1 country

Sites

1

Timeline

Study Start

June 1, 2024

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Primary Completion

September 29, 2024

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Study Completion

October 30, 2024

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Brief Summary

The study aimed to identify the prevalence of GIRD among elite Egyptian volleyball players in selected clubs in Egypt.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: unknown
Estimated enrollment: 70 participants
Study completion date: October 30, 2024
Estimated (date passed)
This estimate has passed. The registry has not confirmed an actual date for this milestone.
Listed locations: 1 countries · 1 sites

Trial Relationships

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Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

First Submitted
May 12, 2024
Actual (reported)
First Posted
May 16, 2024
Actual (reported)
Study Start
June 1, 2024
Estimated (date passed)
This estimate has passed. The registry has not confirmed an actual date for this milestone.
Primary Completion
September 29, 2024
Estimated (date passed)
This estimate has passed. The registry has not confirmed an actual date for this milestone.
Study Completion
October 30, 2024
Estimated (date passed)
This estimate has passed. The registry has not confirmed an actual date for this milestone.

Last Updated: May 16, 2024
Status Verified: May 2024
Last Update Submitted: May 12, 2024

Conditions

Internal Rotation Contracture-shoulder

Keywords

GIRD

Outcome Measures

Primary Outcomes (3)

internal rotation, external rotation and total range of motion
shoulder range of motion
4 months
physical performance
questionnaire
4 months
pain intensity
visual analog scale
4 months

Interventions

bubble inclinometerDevice

to measure range of motion

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age18 Years - 30 Years

Sexall

Healthy VolunteersYes

Age GroupsAdult (18-64)

Sampling MethodProbability Sample

Study Population

professional volleyball athletes from 18 to 30 years old.

You may qualify if:

\. A professional volleyball Egyptian athlete who are playing in the selected clubs around Egypt; the four clubs in Alexandria (Smouha sporting club, Alex sporting club, Ittihad club and Horse owners club) and the three clubs in Cairo (Egyptian shooting club, wadi degla club, Zamalek club).

Sponsors & Collaborators

Cairo University
Otherlead

Study Sites (1)

Faculty of Physical Therapy

Cairo, 4240101, Egypt

RECRUITING

Central Study Contacts

hadeel I ali, master

CONTACT

01148321112 hadeelibrahim241@gmail.com

Study Design

Study Type: observational
Observational Model: COHORT
Time Perspective: CROSS SECTIONAL
Target Duration: 1 Day
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: assistant lecturer

Study Record Dates

First Submitted

May 12, 2024

First Posted

May 16, 2024

Study Start

June 1, 2024

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Primary Completion

September 29, 2024

NCT04787900

Reliability and Validity of iPhone Application for OBER

Not ApplicableCompleted

\. Elite Male and female volleyball players with BMI between (18.5 to 24.9) kg/m².

\. Their age range is between 14 to 30 years old

You may not qualify if:

\. Athletes who have a history of shoulder surgery or injury such as rotator cuff tear or labrum tear.
\. Athletes who have a history of injuries (fractures, dislocations) or surgeries in other joints of the upper limb (elbow, forearm, wrist, and hand) (Dabhokar et al., 2018).
\. Athletes who have a history of inflammatory joint disease, or neurological disorders that could affect their shoulder ROM such as arthritis or diabetes (Dabhokar et al., 2018).
\. Athletes who are taking any medications that could affect their shoulder ROM or pain.
\. Athletes who are currently inactive at the professional level due to multiple injuries that have prevented them from practicing.
\. Athletes who have been diagnosed with kyphosis and scoliosis in the shoulder and thoracic regions, as well as other anatomical anomalies (pennella et al., 2022).
\. Athletes who have experienced shoulder pain with stomach discomfort (pennella et al., 2022)

Contact the study team to confirm eligibility.

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Study Completion

October 30, 2024

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Last Updated

May 16, 2024

Record last verified: 2024-05

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT06416917
Data provider: ClinicalTrials.gov
Source updated: 2024-05-16
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:39:08 UTC

Locations

EG(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

First Submitted

First Posted

Study Start

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (3)

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

Central Study Contacts

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations