Adductor Strain
Conditions
Keywords
Hip adductor, Hip abductor, groin injuries, Copenhagen adductor
Brief summary
This research project will investigate the effects of two 6-week adductor (hip muscle) exercise programmes on adductor muscle function and performance. Measures of adductor muscle strength and performance (jump height, hopping and sprint) and self reported hip and groin function using a questionnaire will be recorded pre and post a 6-week period. A group of footballers will be recruited and randomly allocated to an intervention or control group. Two different intervention groups will complete two different, six-week adductor exercise programmes in addition to their regular training programme. The exercise programmes will last 15 minutes (approximately) per session, with 3 sessions per week. The control group will continue their regular training programme.
Detailed description
Participants will be recruited from the local university sports clubs. Club chairpersons will be asked to send an email to club players. Players interested in participating in the study will be asked to attend a meeting where the study will be explained to them. Those who were interested will then be assessed for inclusion and exclusion criteria. Group allocation: A four block randomization method will be used to allocate participants to the Copenhagen adductor exercise protocol or the adduction and abduction partner exercise protocol. Interventions: Copenhagen adductor exercise protocol or the adduction and abduction partner exercise. Testing procedure: The isometric strength of the participants' hip adductors and abductors will be recorded before and after the exercise intervention. A 10 point visual analogue scale will be used to record the level of muscle soreness experienced after each training session.
Interventions
Week 1 - 1 session per week consisting of 2 sets of 5 reps of the exercise Week 2 - 2 sessions per week consisting of 2 sets of 6 reps of the exercise Week 3 -3 sessions per week consisting of 3 sets of 6 reps of the exercise Week 4 - 3 sessions per week consisting of 3 sets of 8 reps of the exercise Weeks 5 and 6 - 3 sessions per week consisting of 3 sets of the exercise.
OTHERThe adduction and abduction partner exercise
Week 1 - 1 session per week consisting of 2 sets of 5 reps of the exercise Week 2 - 2 sessions per week consisting of 2 sets of 6 reps of the exercise Week 3 -3 sessions per week consisting of 3 sets of 6 reps of the exercise Week 4 - 3 sessions per week consisting of 3 sets of 8 reps of the exercise Weeks 5 and 6 - 3 sessions per week consisting of 3 sets of the exercise.
Sponsors
Dublin City University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)
Eligibility
Sex/Gender
MALE
Age
18 Years to 35 Years
Healthy volunteers
Yes
Inclusion criteria
* free from hip and groin injury in the 6 months prior to the study • currently competing in team sports at least three occasions per week
Exclusion criteria
* history of a hip or groin injury in the 3 months prior to the study * a history of involvement in an adductor strengthening, injury prevention programme in the 3 months prior to the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| isometric hip adductor and abductor strength | Change from baseline after 6 weeks | The maximum isometric hip abductor and adductor strength is assessed with the participant being tested was in supine position, with the test-leg placed at the end of the examination table, and the opposite leg slightly flexed. The dynamometer is placed 5 cm proximal to the proximal edge of the lateral mal¬leolus or 5 cm proximal to the proximal edge of the medial malleolus for hip abduction and adduction, respectively. The dynamometer is externally fix¬ated by the tester's hand/arm placed between the wall and the dynamometer. Participants are initially given two warm up trials of each test of the hip abductors and adductors at 50% and 100% of maximal voluntary isometric force (MVC), followed by three valid MVC trials at the rate of one trial every 60 s |
| Hop test function | Change from baseline after 6 weeks | Single leg hop - the participant will hop as far forwards as possible. Triple hop for distance. Participants will be asked to hop forward three times in a row as far as possible. Crossover hop test. A 3 metre strip of tape will be place on the ground in front of the participants. Participants will be asked to stand on one foot with the tape to the outside of their stance foot. They will then be asked to hop forward three times in a row as far as possible while alternately crossing over the tape and then landing on the same foot, and holding this position for two seconds. Side hop test. Participants will be asked to jump from side to side as many times as possible in 30 seconds without touching the tape. The number of successful jumps will be recorded. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Sprint performance | Change from baseline after 6 weeks | all participants will perform three maximal 30 metre sprint tests with 4 minutes of recovery in between. Time elapsed will be recorded by timing gates placed at 0m, 5m, 15m, and 30m. Participants will start from a standing split position. The first timing gate will be triggered at initial toe off of the back leg. To account for the start of the sprint, a high speed 240Hz iPhone 6 camera and my sprint app will be used to adjust sprint times by calculating the time difference between toe off and the onset of initial movement. The camera will only be focussed on the participant's heel and there will be no images recorded that will identify a participant. Times will be recorded and mechanical sprint variables (maximal horizontal force production, maximal horizontal power output and maximal theoretical velocity) will be calculated using an Excel spreadsheet.The participants best time of the three attempts will be recorded. |
Countries
Ireland
Contacts
Primary ContactEnda whyte, PhD
Backup ContactSiobhan O'Connor, PhD
Outcome results
None listed