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The purpose of this study is to determined if a lower back treatment would change the hip and knee muscle activities in people with and without anterior knee pain. The investigators hypothesized that the lower back treatment may change the hip and knee muscle activities in people with anterior knee pain but not in people without anterior knee pain.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patellofemoral Pain Syndrome | Experimental | Participants with Patellofemoral Pain Syndrome |
|
| Healthy control | Active Comparator | Age- and gender-matched participants without Patellofemoral Pain Syndrome |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Lumbopelvic manipulation | Other | High-velocity-low-amplitude thrust manipulation of the lumbopelvic region |
|
| Measure | Description | Time Frame |
|---|---|---|
| Electromyography (EMG) | Electromyography (EMG) onset time of the gluteus maximus, gluteus medius, vastus medialis oblique, and vastus lateralis muscles. | The EMG data will be collected within 48 hours for all participants in both groups. On Day 1, data will be collected twice at baseline. On Day 2, data will be collected before and immediately after as well as 15, 30, and 45 min after the intervention. |
| Measure | Description | Time Frame |
|---|---|---|
| Pain Visual Analog Scale (VAS) | Pain Visual Analog Scale (VAS) is a 100 mm continuous line between two end-points. The left end-point represents "no pain" and the right end-point represents the "worst pain imaginable". | The Pain Visual Analog Scale (VAS) will be assessed before and 45 min after the lower back treatment (lumbopelvic manipulation) for participants in the patellofemoral pain syndrome group on Day 2 only. |
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Inclusion Criteria for participants in the patellofemoral pain syndrome group:
insidious onset of symptoms of non-traumatic origin
pain with patellar facet palpation or compression
subjective knee pain rating of at least 3/10 on the pain visual analog scale during at least one of the following activities:
Exclusion criteria for all participants:
Age- and gender- matched control participants will be recruited if they have no signs or symptoms of patellofemoral pain syndrome and have none of the exclusion criteria
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| Name | Affiliation | Role |
|---|---|---|
| Ammar M Al Abbad, Master | Texas Woman's University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Texas Woman's University, School of Physical Therapy - Dallas Campus | Dallas | Texas | 75235 | United States |
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| ID | Term |
|---|---|
| D046788 | Patellofemoral Pain Syndrome |
| ID | Term |
|---|---|
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
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