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Clinical Trials/NCT07124429
NCT07124429CompletedNot Applicable

A Comparative Evaluation of the Effects of Reformer Pilates and Standard Physiotherapy on Rehabilitation After Femoral Lengthening Surgery.

Istanbul Medipol University Hospital1 site in 1 country30 target enrollmentStarted: January 11, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
Muscle strength assessments

Study Overview

Brief Summary

The femur, which forms the foundation of the lower extremity's skeletal system, is one of the most critical bones in the human body due to both its structural integrity and its functional duties.

Detailed Description

Surgical interventions aimed at correcting femur length have held a very important place in the development of orthopedic surgery.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Investigator)

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Aged between 18 and 45 years
  • •Male gender
  • •Having undergone bilateral femoral lengthening surgery for cosmetic purposes only
  • •The lengthening operation having been performed solely with the LON technique

Exclusion Criteria

  • •Female patients
  • •Patients who have undergone unilateral femoral lengthening surgery
  • •Patients under 18 or over 45 years of age

Arms & Interventions

Reformer Pilates

Experimental

Reformer Pilates

Intervention: Reformer Pilates (Other)

conservative treatment

Active Comparator

conservative treatment

Intervention: conservative treatment (Other)

Outcomes

Primary Outcomes

Muscle strength assessments

Time Frame: 8 weeks

Muscle strength assessments were performed using a MicroFET brand handheld dynamometer.

Daily Living Activities

Time Frame: 8 weeks

Functional status was assessed using the Barthel Activities of Daily Living Index, which ranges from 0 (total dependence) to 100 (complete independence), with higher scores indicating a better outcome.

Muscle shortness

Time Frame: 8 weeks

Muscle shortness was measured using standard clinical evaluation methods. The quadriceps femoris and hamstring muscles are major opposing groups in the thigh, while the tensor fasciae latae (TFL) is a key muscle involved in hip movements.

Muscle Reaction Time

Time Frame: 8 weeks

The BlazePod TTM (Play Coyotta Ltd.) device was used for the assessment of muscle reaction time. This device is a wireless system consisting of LED lights and a central controller, and it's designed to measure a participant's response time to specific light signals.

Pain Assessment

Time Frame: 8 weeks

Participants' pain levels were evaluated using the Visual Analog Scale (VAS). All data was collected by a physiotherapist in a one-on-one session within a clinical setting and manually recorded on standard evaluation forms.

Joint Range of Motion

Time Frame: 8 weeks

Joint range of motion measurements were evaluated separately for the right and left sides using a standard goniometer

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Istanbul Medipol University Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

hazal genc

Principal Investigator

Istanbul Medipol University Hospital

Study Sites (1)

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