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Effect of Induced Rotator Cuff Muscles Fatigue on Hand Grip Strength in Adults

N

Noura Karam Abdou Mohammed Ismaiel

Status

Not yet enrolling

Conditions

Healthy Individuals

Treatments

Device: Induced rotator cuff fatigue by isokinetic biodex

Study type

Observational

Funder types

Other

Identifiers

NCT07054853
P.T.REC/012/005798

Details and patient eligibility

About

This observational study aims to investigate the effect of induced rotator cuff muscles fatigue on hand grip strength in adults

Full description

This study is set to take place at the Isokinetic Biodex Laboratory, Faculty of Physical Therapy at Misr University for Science and Technology (MUST). The goal is to explore how fatigue in the rotator cuff muscles affects hand grip strength in healthy adults.

The study will involve 30 healthy male and female participants, aged between 18 and 30 years, all recruited from the university. To ensure the reliability of the results, participants must meet specific inclusion criteria: they should have no recent history of shoulder or back pain, no spinal deformities, and a body mass index within the normal range. Individuals with any upper limb disorders, recent surgeries, or neurological issues will be excluded.

The experimental protocol is carefully structured and will be conducted using two key tools. The first is the Biodex System 4 Pro, an isokinetic dynamometer renowned for its accuracy in measuring muscle performance and fatigue. The second is the Jamar Plus+ Digital, a gold-standard device for measuring grip strength, known for its reliability and ease of use.

Participants will attend two fatigue sessions apart to prevent carryover effects. Each session will involve a fatigue protocol by isokinetic biodex system targeting the shoulder's internal and external rotators at two different abduction angles: 30° (Protocol A) and 90° (Protocol B).

Grip strength will be assessed both before and after each fatigue session using the Jamar plus+ Digital. Participants will sit with their arms and legs positioned for standardized testing, and each will complete three maximal grip trials. The average of these attempts will be recorded, with verbal encouragement provided to ensure maximal effort.

Through this structured investigation, the study aims to shed light on how rotator cuff fatigue influences hand grip strength-an insight that could have practical implications for injury prevention, rehabilitation strategies, and performance optimization in both clinical and athletic settings.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Both male and females (18-30) years
  • No complaints of existing shoulder pathology/pain in at least one shoulder within the last 6 months, no back pain, no history of shoulder/thoracic spine surgery, and no spinal deformities
  • Body mass index between (18.5:24.99) Kg/ m2

Exclusion criteria

  • Shoulder complaints in the past 6 months such as shoulder dislocation rotator cuff tear, shoulder surgery, and shoulder rehabilitation or other upper limb forms of disability
  • Subjects who had wrist pain, a joint injury, undergone surgery, or neuromuscular dysfunction were excluded from the study
  • Individuals who suffered an injury or underwent a surgical procedure in the last six months that could affect hand functions or senses

Trial design

30 participants in 1 patient group

one group males and females
Treatment:
Device: Induced rotator cuff fatigue by isokinetic biodex

Trial contacts and locations

1

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Central trial contact

Noura K. Ismaiel, Bachelor's degree

Data sourced from clinicaltrials.gov

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