Hip manipulation to improve strength in patients with hip pain
Effects of Unrestrained Femoral Internal Rotation Manipulation on Hip External Rotation Strength in Individuals with Nonspecific Hip Pain: a One-Week Follow-Up Clinical Trial
This study is testing if a special hip manipulation can help people with hip pain get stronger and feel better compared to those who receive a fake treatment.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 24 (estimated) |
| Ages | 18 Years to 55 Years |
| Sex | All |
| Sponsor | Andrews University Academic / other |
| Locations | 1 site (Columbia, Maryland) |
| Trial ID | NCT06655987 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of an unrestrained femoral internal rotation (UFIR) manipulation technique on hip external rotation strength in individuals experiencing nonspecific hip pain. It aims to determine whether this joint manipulation can enhance hip function and reduce pain compared to a control group receiving sham manipulation. The study will involve 24 adults aged 18-55 with hip pain and weakness, assessing their strength through manual muscle testing and dynamometry at various intervals. The findings may provide insights for physical therapists regarding alternative treatment approaches for hip pain.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-55 with nonspecific hip pain and ipsilateral hip external rotation weakness.
Not a fit: Patients with severe hip conditions, cognitive impairments, or those requiring assistive devices for balance may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment options for patients suffering from hip pain and weakness.
How similar studies have performed: While there is limited research on UFIR manipulation specifically, similar joint manipulation techniques have shown promise in improving strength and function in other contexts.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * individuals who meet the following inclusion criteria will be eligible to participate in this study: 1) nonspecific hip pain, 2) ipsilateral hip external rotation weakness (at or below 3+) based on the MMT test Exclusion Criteria: * individuals who meet any of the following exclusion criteria will not be eligible to participate in this study: 1) do not speak English, 2) have an impaired cognition and are unable to follow multi-step commands, 3) require an assistive device for standing balance, 4) have complaints of intractable (intolerable) pain, 5) have a history of hip dislocation or total hip replacement, 6) have a history of hip fracture or arthroscopy in the past 6 months, 7) have a history of lumbar spine fracture or surgery (e.g., lumbar discectomy and fusion) in the past 6 months, 8) present with neurological condition (i.e., stroke, Parkinson's disease, or lumbar radiculopathy), 9) known congenital hip dysplasia/adolescent hip disease, and 10) known osteoporosis
Where this trial is running
Columbia, Maryland
- SKYE Physiotherapy — Columbia, Maryland, United States (Recruiting)
Study contacts
- Study coordinator: Chang Min Lee
- Email: info@skyephysiotherapy.com
- Phone: (410) 357-6500
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.