Effect of Induced Rotator Cuff Muscles Fatigue on Hand Grip Strength in Adults
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 34
- Locations
- 1
- Primary Endpoint
- Hand Grip Strength
Study Overview
Brief Summary
This observational study aims to investigate the effect of induced rotator cuff muscles fatigue on hand grip strength in adults
Detailed 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.
Study Design
- Study Type
- Observational
- Observational Model
- Other
- Time Perspective
- Cross Sectional
Eligibility Criteria
- Ages
- 18 Years to 30 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
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
Arms & Interventions
one group males and females
Intervention: Induced rotator cuff fatigue by isokinetic biodex (Device)
Outcomes
Primary Outcomes
Hand Grip Strength
Time Frame: 3 months
Maximum Voluntary Contraction
Secondary Outcomes
No secondary outcomes reported
Investigators
Noura Karam Abdou Mohammed Ismaiel
Teaching Assistant
Cairo University