Dynamic Knee Valgus, Injury Prevention
Conditions
Brief summary
The primary aim of this randomized controlled trial is to investigate the effectiveness of 6 weeks of progressive resistance training (PRT) compared to neuromuscular training (NMT) on functional performance in healthy female participants as measured by the Single-Leg Landing (SLL) and Single-Leg Squat (SLS) tests. The secondary aims are to investigate the, * change in abduction hip muscle strength, which will be measured with a Biodex System 3 Isokinetic Dynamometer. Outcomes will be measured at baseline and after 6 weeks of intervention. * adherence to the 6-week initial intervention (High adherence is defined as ≥ 80% attendance to the supervised interventions.)
Detailed description
Participants will be randomized into two groups: PRT or NMT. Outcomes will be measured at baseline and after 6 weeks of intervention. All sessions will be conducted in group sessions, with one researcher supervising the exercises. Patients receive education as well as supervised exercise from trained physiotherapists. Each session will last approximately 25-30 minutes. The duration of the program will be 6 weeks, with 3 sessions every week (total: 18 training sessions). The NMT intervention sessions consist of a 5-minute submaximal warm-up followed by 25 minutes of NMT training with exercises focused on functional stability, proprioception, strength, stability, agility, postural function, and postural orientation. The training sessions will consist of two parts: warming up and the circuit program. The circuit program will consist of 8 exercises. Each exercise will be performed for 2 sets of 10 repetitions, with a rest of 30 sec corresponding to every set, between each set and exercises. The exercises will be focused on one knee, which will then be evaluated. Three levels of difficulty will be given for each exercise to allow for progression. Every 2 weeks, there will be a progression that will be achieved by changing the exercise and gradually making it harder, or/and changing the support surface. In the PRT intervention, the sessions will consist of a 5-minute submaximal warm-up followed by 20 minutes of PRT with exercises targeting the abductor muscles of the hip joint. The circuit program will consist of three exercises. Each exercise will be performed in sets of three, then increased to four sets of ten repetitions, with a 30-second rest between each set and exercise. The exercise intensity will be monitored by the researcher, as determined by the patient's ability to complete three sets of 8-12 repetitions for a given exercise and a Borg Rating of Perceived Exertion (RPE) of 6-10. The progression will be in line with guidelines provided by the American College of Sports Medicine. Adherence to the program for both groups will be assessed by the total number of training sessions performed in 6 weeks (total = 18 training sessions).
Interventions
The 6-week exercise intervention consists of 25-minute group sessions of Neuromuscular training supervised by a researcher.
OTHERHip abductors muscular strength exercises
The 6-week exercise intervention consists of of 20-minute group sessions of progressive resistance training, supervised by a researcher.
Sponsors
University of Thessaly
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
Yes
Inclusion criteria
* female gender * older than 18 and younger than 35 years of age * physically able to perform physical activities and exercise * participants should know the greek language in order to understand the instructions and be able to read the consent form
Exclusion criteria
* undergoing treatment for lower extremity injury * currently experiencing an average overall pain severity ≥3 out of 10 on an 11-point numerical rating scale in the past week * history of knee pain in the proceeding twelve months, history of lower limb surgery, known rheumatologic, neurological or cardiovascular disorders with raised blood pressure
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes in knee kinematics measured during a Single-Leg Squat functional test | Measured at baseline and Week 6. | Dynamic Knee Valgus (recorded in degrees) will be assessed during a Single-Leg Squat test. Changes during the test will be analyzed with the Kinovea program. |
| Changes in knee kinematics measured during a Single-Leg Landing functional test | Measured at baseline and Week 6. | Dynamic Knee Valgus (recorded in degrees) will be assessed during a Single-Leg Landing test. Changes during the test will be analyzed with the Kinovea program. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in abduction hip muscle power | Measured at baseline and Week 6. | Change in abduction hip muscle power (measured in Newtons) will be measured with a Biodex System 3 isokinetic dynamometer. |
| Adherence to the 6-week initial intervention | Measured at Week 6. | High adherence is defined as ≥ 80% attendance to the supervised interventions. |
Countries
Greece
Outcome results
None listed