Anterior Cruciate Ligament Injuries Clinical Trial
Official title:
Combined Effect Of Blood Flow Restriction Technique And Conventional Physical Therapy Program After Anterior Cruciate Ligament Reconstruction
The purpose of this study will be to evaluate the effect of adding BFR (using 80% of LOP) to the conventional physical therapy program on knee function, functional test, balance, quadriceps and hamstrings muscles strength, thigh muscle girth and knee effusion in rehabilitation after ACLR.
| Status | Not yet recruiting |
| Enrollment | 30 |
| Est. completion date | July 1, 2025 |
| Est. primary completion date | June 1, 2025 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 35 Years |
| Eligibility | Inclusion Criteria: 1. Aged from 18-35 years. 2. Underwent an ACLR semitendinosus autograft one-week post-operative 3. Willingness to participate in the intervention and subsequent assessment. 4. BMI from 18.5 to 29.9 kg/m2. Exclusion Criteria: 1. Insecure graft fixation (due to bone quality, suspension). 2. Active infection. 3. Postsurgical excess knee swelling that may limit exercise performance. 4. ACLR using bone tendon bone (BTB) graft. 5. Any cardiovascular disease such as hypertension. 6. Any lower limb trauma. 7. Hip and ankle pathology. 8. BMI more than 30 kg/m2 |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Cairo University |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | knee function | will be assessed by the Arabic version of the knee outcome survey-activities for daily living scale.
It encompasses six questions addressing restrictions in daily activities caused by symptoms like pain, swelling, and instability, and eight questions evaluating difficulties in functional tasks such as walking, stair climbing, and sitting or standing up from a chair. Each question is rated on a 6-point Likert scale. Scores range from 0 to 70, with higher scores indicating better functional capacity. |
after 3 months of intervention | |
| Primary | knee functional test | will be assessed by the single leg hop test | after 3 months of intervention | |
| Primary | balance | will be assessed by the Y balance test for the lower quarter | after 3 months of intervention | |
| Primary | quadriceps and hamstring muscles strength | will be assessed by the hand held dynamometer | after 3 months of intervention | |
| Secondary | Thigh muscle girth | will be assessed by a non-elastic measuring tape | baseline then 3 months after intervention | |
| Secondary | Knee effusion | will be assessed by a non-elastic measuring tape | baseline then 3 months after intervention |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
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