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The Relationship Between Thicknesses and Isokinetic Strength of Hip Flexor and Extensor Muscles

The Evaluation of the Relationship Between Thicknesses and Isokinetic Strength of Hip Flexor and Extensor Muscles in Patients With Unilateral Traumatic Transfemoral Amputation

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05827744
Enrollment
27
Registered
2023-04-25
Start date
2023-05-15
Completion date
2023-12-15
Last updated
2023-10-23

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

Conditions

Amputation, Traumatic

Keywords

amputation, hip flexors, hip extensors

Brief summary

The aim of this study is to investigate the relationship of hip muscle thicknesses measured by ultrasonography with hip flexion and extension strength and clinical parameters in prosthesis users with unilateral traumatic transfemoral amputation.

Detailed description

The aim of this study is to investigate the relationship of hip muscle thicknesses measured by ultrasonography with hip flexion and extension strength and clinical parameters in prosthesis users with unilateral traumatic transfemoral amputation. This study will be useful in understanding whether ultrasonography is an appropriate imaging method in the follow-up of changes in functional strength in the hip girdle in patients with unilateral traumatic transfemoral amputation.

Interventions

OTHERIsokinetic evaluations

Peak torque and total amount of work of hip flexors and extensors will be determined by the Cybex 6000 model computer-aided isokinetic system.

Ultrasonographic evaluations will be performed with a 5-12 MHz linear probe (Logic e portable; GE Healthcare, China). The thicknesses of the hip flexor (psoas major) and extensor (gluteus maximus) muscles will be measured while the patient is in the prone position, in accordance with the literature.

Sponsors

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
MALE
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Aged between 18-65 * The time elapsed after amputation \> 6 months * Using prosthesis for at least 3 months * Being able to walk without an assistive device

Exclusion criteria

* Bilateral lower extremity amputation * Presence of neurological, cardiovascular, and pulmonary disease that may affect walking performance

Design outcomes

Primary

MeasureTime frameDescription
6-minute walking test (6MWT)through study completion, an average of one monthFunctional performance will be assessed by 6MWT (in meter). Patients will be instructed to walk quickly, safely, and as much distance as possible over a rectangular path.
10-meter walking testthrough study completion, an average of one monthThe short-distance over-ground gait speed will be assessed using a 10-Meter Walk Test. Participants will be asked to walk at normal pace on a 10-meter walkway.
Timed up and go testthrough study completion, an average of one monthTimed up and go test will be used for quantifying functional mobility balance. Participants will be instructed to sit in a comfortable position on a 45-65 cm high steady chair with a backrest and armrest, with both arms resting on their thighs, and then quickly stand up and move towards and around a fixed cone 3 m away, return, and sit again.

Countries

Turkey (Türkiye)

Contacts

Primary ContactMerve Örücü Atar, MD
drmerveorucu@hotmail.com03122912443

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026