The Acute Effect of Foam Rolling on Elbow Joint Sensorimotor Function
NCT ID: NCT03516149
Last Updated: 2019-02-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
60 participants
INTERVENTIONAL
2018-08-20
2018-11-20
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Influence of Foam Rolling on Elbow Proprioception, Strength, and Functional Motor Performance
NCT03312062
Effect of Genicular Nerve Block on Proprioception in Knee Osteoarthritis
NCT06744842
Different Proprioceptive Neuromuscular Facilitation (PNF) Technique in Patients With Knee Osteoarthritis
NCT03615521
Investigation The Efficacy of Manual Therapy and Exercise in Patients With Glenohumeral Arthritis
NCT03958227
Physical Therapy on Non-structural Medial Elbow Pain
NCT05537636
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Foam rolling exercise will be applied 10 times each for 1 minute. These exercise will be performed as 2 sets. After each set will be a resting period for 30 seconds. A total of 1 session will be performed. Second evaluation will be performed after exercise at the same day. Control group will receive no foam rolling exercise. They will be handed a brochure about the proprioception and its role in injury prevention and foam rolling. Control group will be evaluated for the first time. Afterwards, second evaluation will be performed after resting period (2 minutes) at the same day.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Foam Rolling Group
The participants in this group will receive foam rolling exercise.
Foam Rolling Exercise
Foam rolling exercise will be performed actively. Participants will use a foam roller for exercise. They will position the foam roller on the chair. Afterwards, they will use their body weights to rub the elbow area (biceps brachii muscle) with this foam. There will be 2 sets and each set will be 1 minute. Single set contains 10 repetitions in 1 minute with 30 seconds resting period between sets
Control Group
The participants in this group will receive no foam rolling. They will only be evaluated.
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Foam Rolling Exercise
Foam rolling exercise will be performed actively. Participants will use a foam roller for exercise. They will position the foam roller on the chair. Afterwards, they will use their body weights to rub the elbow area (biceps brachii muscle) with this foam. There will be 2 sets and each set will be 1 minute. Single set contains 10 repetitions in 1 minute with 30 seconds resting period between sets
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* No pain in elbow area within 6 months and at the time of measurement
* To be able to complete all evaluations and applications to be carried out
Exclusion Criteria
* Having acne and similar skin problems, open wounds
* Having upper extremity injury, history of fracture or surgery
* Having any systemic musculoskeletal disease
* Having diagnosis of diabetic mellitus or peripheral neuropathy
* Having osteoporosis diagnosis
* Having any cardiovascular disease
* Having vertigo
* Being pregnant
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Dokuz Eylul University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Fatma Özden, PT
Physical Therapist
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Sevgi Sevi Yeşilyaprak, Phd
Role: STUDY_DIRECTOR
Dokuz Eylul University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Fatma Özden
Izmir, Bornova, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
3470-GOA
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.