NCT06851689

Brief Summary

The aim is to reduce the incidence of hand grip weakness and shoulder rotation torque decline. this proposed study aims to suggest solutions to prevent occurring injuries

Trial Health

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
46

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Feb 2025

Shorter than P25 for all trials

Status
not yet recruiting

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 23, 2025

Completed
5 days until next milestone

First Posted

Study publicly available on registry

February 28, 2025

Completed
Same day until next milestone

Study Start

First participant enrolled

February 28, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 30, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2025

Completed
Last Updated

February 28, 2025

Status Verified

February 1, 2025

Enrollment Period

1 month

First QC Date

February 23, 2025

Last Update Submit

February 26, 2025

Conditions

Keywords

hand gripshoulder torqueacademic staff

Outcome Measures

Primary Outcomes (2)

  • hand grip strength

    assess hand grip

    2 months

  • shoulder torque

    assess peak shoulder torque of rotator muscle

    2 months

Interventions

Jamar handheld dynamometer to asses hand grip strength

Biodex isokinetics to asses torque

Eligibility Criteria

Age25 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Healthy adult academic staff

You may qualify if:

  • University teaching staff who work full time at Misr University for Science and Technology. (average 7 hours per day)
  • Both male and female participants between 25 and 45 years of age
  • Participants without any pain or musculoskeletal disorder
  • Participants who perform overhead activities during teaching
  • The range of BMI is between 18.5-25 in the normal range
  • Both right and left handed subjects are included

You may not qualify if:

  • Recent history of shoulder, upper limb, neck or thoracic fracture or surgery
  • \. Neurological disorders affecting the upper limb
  • \. Regional tumor or metastasis of the upper limb
  • \. Academicians with trauma or injury within the past 6 months, or known pregnancy
  • \. Engagement of any vigorous exercise or work after university hours
  • History of surgery within the past six months, epilepsy, or chronic neurologic disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Abanoub Emeil Melad, Bachelor

    Misr University for Science and Technology

    PRINCIPAL INVESTIGATOR
  • Neveen Abdel-Latif, professor

    Cairo University

    STUDY CHAIR
  • Rania Reda, Ass.prof

    Cairo University

    STUDY DIRECTOR
  • Mohamed Farouk, lecturer

    Misr University for Science and Technology

    STUDY CHAIR

Central Study Contacts

Abanoub Emeil Melad, Bachelor

CONTACT

Abanoub Emeil Melad, Bacherol

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principle investigator

Study Record Dates

First Submitted

February 23, 2025

First Posted

February 28, 2025

Study Start

February 28, 2025

Primary Completion

March 30, 2025

Study Completion

May 1, 2025

Last Updated

February 28, 2025

Record last verified: 2025-02

Data Sharing

IPD Sharing
Will not share