- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06644989
Impact of Osteopathic Manipulative Therapy on Hip Range of Motion
Impact of Spencer's Technique of the Hip on Hip Range of Motion in Recreational Runners
One way for runners to improve their performance and remain injury free is to preserve and improve joint mobility, especially at the hips. The femoroacetabular joints are a pivotal part of the running gait allowing the athlete to fully extend their leg to generate sufficient force in each stride. Improving hip range of motion can help reduce or prevent groin pain, make the runner more comfortable while running, improve running longevity, and prevent injuries. Thus, it is clear that a runner's commitment to improving the range of motion of their hips is crucial for both the enhancement of their performance and prevention of injury. Researchers assessed how the hip, and its biomechanics, can be impacted by Osteopathic medical treatment.
The primary research question investigated is how Spencer Technique for the hip impacts femoral acetabular active range of motion (AROM) in flexion, extension, abduction, adduction, internal rotation, and external rotation in those training 4 weeks for a 5K race. This study investigated the effect that 4 weeks of twice weekly, bilateral, Spencer Technique treatment had on femoroacetabular range of motion. During this 4-week period participant exercise and stretching habits in preparation for the 5k race were recorded.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Florida
-
Bradenton, Florida, United States, 34211
- LECOM
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- All LECOM-Bradenton students will be included in recruitment.
Exclusion Criteria:
Subjects will be excluded from this research study if they cannot sign an informed consent. Additionally, subjects will be excluded if they are:
- Pregnant or plan to become pregnant
Have a past medical history including:
- Skin disorders or open wounds precluding skin contact
- Neurological symptoms (i.e. numbness, tingling, weakness)
- Recent bone fracture
- Recent lower extremity ligamentous sprain
- Recent lower extremity muscle strain
- Adhesive capsulitis of the hip joint
- Osteoarthritis of the lower extremity
- Rheumatoid arthritis
- History of hip or knee arthroplasty
- 1 year history of any lower extremity surgery
- Gout
- Iliotibial band syndrome
- Legg-Calve-Perthes disease
- Slipped capital femoral epiphysis
- Hip dysplasia
- Avascular necrosis of the hip
- Chronic hip bursitis
- Hip dislocation
- Osteoporosis/osteopenia
- Severe Femoroacetabular impingement
- Use of heel lift due to leg length discrepancy
- Immunosuppressive syndromes
- Radiation or chemotherapy within the past 3 years
- Congestive heart failure
- Unable to complete a 5 kilometer race after the 4 weeks of training
- Down syndrome
- Have been told by a physician or other medical professional that you should not participate in aerobic training activities.
- Have medication changes in the last month
- Run 30+ miles per week regularly
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Sham Comparator: Sham Comparator
Half of Participants receive Spencer technique and half of participants received a sham treatment.
|
Spencer technique position but no pressure
|
|
Experimental: Experimental
Half of Participants receive Spencer technique and half of participants received a sham treatment.
|
Spencer technique on the hip
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Range of Motion
Time Frame: 4 weeks
|
Hip range of motion (flexibility) is measured to monitor changes in flexibility
|
4 weeks
|
Collaborators and Investigators
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Protocol 31-085
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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