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Degenerative changes in the hamstrings and extracorporeal shock wave therapy in patients with hip fractures

Degenerative Hamstring Changes as Correlates of Falls and Hip Fracture Prevalence

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0011289
Enrollment
90
Registered
2025-12-10
Start date
2025-12-10
Completion date
Unknown
Last updated
2026-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : Extracorporeal Shock Wave Therapy (ESWT): Standard rehabilitation plus extracorporeal shock wave therapy (ESWT) applied to the proximal hamstring origin (sciatic tuberosity area). • I

Sponsors

Hallym University Medical Center-Kangnam
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The selection criteria are as follows: Patients aged 65 years or older with a unilateral hip fracture who were treated at this institution during the study period and underwent surgical treatment were eligible for the study. Participants must have been able to walk independently before surgery, understood the purpose and procedures of the study, voluntarily provided written consent, and were able to understand and follow simple instructions.

Exclusion criteria

Exclusion criteria: The exclusion criteria are as follows: bilateral hip fractures or multiple fractures, inability to walk independently without a walking aid before surgery, inability to carry out the study instructions due to severe cognitive decline, medical instability after surgery that results in a contraindication to rehabilitation treatment (e.g., deep vein thrombosis, pulmonary embolism, uncontrolled cardiovascular disease, etc.), prescription of non-weight bearing at the surgical site, history of neurological disease such as stroke or Parkinson's disease that affects gait, participation in another rehabilitation program during the study period, or participation in the study deemed inappropriate by the researcher's medical judgment.

Design outcomes

Secondary

MeasureTime frame
Cumulated Ambulation Score, CAS;Modified Gait Efficacy Scale(mGES);Timed Up and Go Test (TUG);Pain(NRS);Number of days hospitalized;Dependence on assistive devices

Primary

MeasureTime frame
Days to First Ambulation

Countries

Korea, Republic of

Contacts

Public ContactJaeyoung Lee

Hallym University Medical Center-Kangnam

2wo02wo0@naver.com+82-2-829-5165

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026