Understanding Greater Trochanteric Pain Syndrome
Clinical Characteristics and Subgroups in Greater Trochanteric Pain Syndrome
This study is trying to learn more about Greater Trochanteric Pain Syndrome by collecting information from people who have it to see what factors might affect how well treatments work.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 150 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | NHS Greater Glasgow and Clyde Academic / other |
| Locations | 1 site (Glasgow) |
| Trial ID | NCT06026579 on ClinicalTrials.gov |
What this trial studies
This observational study aims to collect data from individuals diagnosed with Greater Trochanteric Pain Syndrome (GTPS) through clinical assessments and questionnaires. GTPS is characterized by pain around the greater trochanter, often due to gluteal tendinopathy, which can severely impact daily activities and quality of life. The study seeks to identify clinical characteristics that may influence treatment outcomes, as current exercise programs are not effective for a significant portion of patients. By analyzing these factors, the research hopes to improve understanding and management of GTPS.
Who should consider this trial
Good fit: Ideal candidates for this study are adults over 18 years old with lateral hip pain and a clinical diagnosis of Greater Trochanteric Pain Syndrome.
Not a fit: Patients with lateral hip pain due to other sources, such as hip joint pathology or inflammatory conditions, may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to more personalized treatment strategies for patients suffering from Greater Trochanteric Pain Syndrome.
How similar studies have performed: While there have been studies on GTPS, this approach focusing on individual clinical characteristics is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults aged \> 18 years who currently reside within Greater Glasgow and Clyde * Lateral hip pain of any duration * Able to give written informed consent * Pain on direct palpation of the gluteal tendon insertion on the greater trochanter and additionally at least one of the following pain provocation tests must also be positive: 1. FABER (Flexion, Abduction, External Rotation of the hip) 2. FADER (Flexion, Adduction, External Rotation of the hip) 3. FADER and resisted Internal Rotation (IR) (FADER position plus resisted IR of the hip) 4. Single leg stand for 30 seconds 5. Resisted hip abduction at end-range adduction Exclusion Criteria: * Lateral hip pain secondary to another source e.g. hip joint pathology or lumbar referred pain * Inflammatory joint conditions * Neurological conditions * Pregnancy * Unable or unwilling to give informed consent * Unable to write, read or comprehend English
Where this trial is running
Glasgow
- NHS Greater Glasgow and Clyde — Glasgow, United Kingdom (Recruiting)
Study contacts
- Principal investigator: Chris Clifford, PhD — NHS Greater Glasgow and Clyde
- Study coordinator: Chris Clifford, PhD
- Email: chris.clifford@ggc.scot.nhs.uk
- Phone: 0141 347 8685
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.