- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06168240
The Effect of Manual Lymphatic Drainage on Acute and Post-acute Ankle Sprain in Athletes
THE EFFECT OF MANUAL LYMPHATIC DRAINAGE ON ACUTE AND POST-ACUTE ANKLE SPRAIN IN ATHLETES
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study will examine the effect of manual lymphatic drainage on pain intensity, ankle swelling, range of motion, static and dynamic functional stability in acute and post-acute ankle sprain in athletes.
Edema treatment includes a variety of techniques; elevation, compression, electrical stimulation, ultrasound, and massage are a few of them. Profound clinical check is required to determine the kind of edema management. However, the effect of these techniques on the lymphatic system and the edema itself is questionable. Manual Lymphatic Drainage mechanism, although still under investigation, is also a valid treatment management that does not cause inflammation, reduces the absorption of waste products and excess fluid and still urges the lymphatic system to work better.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- . Basketball Athletes patients diagnosed as acute and post-acute ankle sprain. 2. Patients within 18 and 30 years old. 3. Patients with grade I, II ankle inversion sprain. 4. All participants complains of pain and moderate swelling in the ankle.
Exclusion Criteria:
- Previous ankle surgery.
- Serious pathology.
- History of fractures in the ankle joint.
- Vascular disorders.
- Grade III ankle sprain.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: group A
will receive Manual lymphatic drainage plus Traditional physical therapy program that will include LASER, cold packs, manual mobilization, and exercise program.
Training will applied 3 days a week, for a total of 4 weeks.
|
Training will applied 3 days a week, for a total of 4 weeks.
Other Names:
|
|
Active Comparator: group B
will receive Traditional physical therapy program only that will include LASER, cold packs, manual mobilization, and exercise program.
Training will applied 3 days a week, for a total of 4 weeks.
|
Training will applied 3 days a week, for a total of 4 weeks.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
static balance
Time Frame: starting and after 4 weeks
|
Flamingo Balance Test to assess static balance
|
starting and after 4 weeks
|
|
dynamic postural balance
Time Frame: starting and after 4 weeks
|
Star Excursion Balance Test to assess dynamic postural balance
|
starting and after 4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
swelling
Time Frame: starting and after 4 weeks
|
Figure of Eight with tape measurement by tape measurement to assess swelling in centimeter
|
starting and after 4 weeks
|
|
range of motion
Time Frame: starting and after 4 weeks
|
Goniometer to assess range of motion
|
starting and after 4 weeks
|
|
Pain intensity
Time Frame: starting and after 4 weeks
|
Numeric Pain Rating Scale to assess pain intensity with zero score represents no pain (the better) and ten score represents maximum pain (the worest).
|
starting and after 4 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 012/003909
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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