Assessment of Effectiveness of Neuromuscular Training in Treatment of Lumbar Spine in Football Players
NCT ID: NCT04134741
Last Updated: 2019-10-22
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
18 participants
INTERVENTIONAL
2019-01-03
2019-06-16
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The study was designed as single-blind Randomized Controlled Trial (RCT) and conducted on a group of 18 female football players from University Club of the Academic Sports Association of Pope John Paul II State School of Higher Education in Biała Podlaska. Participants were randomly divided into two 9-person groups: A - used standard training and neuromuscular training (Kinetic Control) and B - used only standard training.
Main hypothesis:
The application of neuromuscular therapy (KC) reduces the risk of injuries and pain of the lumbar spine and the knee and improves the static and dynamic balance.
Research questions:
1. Will the application of the KC training reduce the risk and frequency of spine and knee injuries in females football players?
2. Will the KC training lead to reduction of the intensity of lumbar spine and knee pain?
3. Will the application of the KC training lead to increase in the torque strength of knee flexors and extensors and improved stability of the knee?
4. Will the application of the neuromuscular training (KC) lead to reduction of the disability level and improved functional level?
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Functional Exercises for Chronic Low Back Pain
NCT03376724
Effect of Knee Extensor Training on the Lumbar Spine
NCT07337213
The Effectiveness of Manual Therapy and PNF Compared With Kinesiotherapy in the Treatment of Non-specific Low Back Pain
NCT03733964
Evaluation of the Kinesiology Taping Effectiveness in the Treatment of Lumbar Spine Pain
NCT05104957
Feasibility of a One-day-and-a-half for Patients With Low Back Pain
NCT04133818
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The study was designed as single-blind Randomized Controlled Trial (RCT) and conducted on a group of 18 female football players from University Club of the Academic Sports Association of Pope John Paul II State School of Higher Education in Biała Podlaska. Participants were randomly divided into two 9-person groups: A - used standard training and neuromuscular training (Kinetic Control) and B - used only standard training.
None of the physiotherapists were personally involved in the preparation and the manner of performing the test. Before commencing the tests, each participant was familiarised with their course, expressed their informed written consent for the participation and random assignment to the specified tested group.
The random placement was performed with the use of computer software.
The players participate in two training cycles over a year: from July to December and from January to June. Therefore, the above mentioned training regime will be performed twice.
A medical interview takes place before the training cycle. Physical examination, back pain functional scale (BPFS) and tests on the dynamographic platform will be performed two times - before and after each season.
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
The random placement was performed with the use of computer software.
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Kinetic Control Group
The players participated in the classic training and for 4 weeks (3 times a week) underwent the Kinetic Control neuromuscular training with assistance of a physical therapist.
The duration of one training was 20-30 minutes.
Kinetic Control
The Kinetic Control training included a functional examination of motor disorders and individual training. The KC training included active exercises, active exercises with torso muscle resistance and exercises involving lower limbs.
The duration of one training was 20-30 minutes.
Traditional Training Group
Players participated in the classic training.
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.
Kinetic Control
The Kinetic Control training included a functional examination of motor disorders and individual training. The KC training included active exercises, active exercises with torso muscle resistance and exercises involving lower limbs.
The duration of one training was 20-30 minutes.
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* written consent for the participation in the study.
Exclusion Criteria
* female players who suffered from a lumbar spine and/or knee injury up to 6 months before the start of the study,
* female players with acute knee inflammation and after knee surgeries.
19 Years
25 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
John Paul II University in Biała Podlaska
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Kamil Zaworski, PhD
Role: STUDY_DIRECTOR
John Paul II University in Biała Podlaska
Anna Kręgiel, PhD
Role: PRINCIPAL_INVESTIGATOR
John Paul II University in Biała Podlaska
Krystyna Gawlik, PhD
Role: STUDY_CHAIR
John Paul II University in Biała Podlaska
Joanna Baj-Korpak, PhD
Role: PRINCIPAL_INVESTIGATOR
John Paul II University in Biała Podlaska
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Pope John Paul II State School Of Higher Education in Biała Podlaska
Biała Podlaska, , Poland
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.
PopeJohnPaulIIStateSchHigherEd
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.