Functional Effects of Postoperative Physiotherapy After Cosmetic Femoral Lengthening (LON-PT)
LON-PT
1 other identifier
interventional
54
1 country
1
Brief Summary
This study aims to understand how an early postoperative conventional physiotherapy program affects daily movement and physical function in adults who undergo cosmetic femoral lengthening surgery using the Lengthening Over Nail (LON) technique. Participants aged between 18 and 45 years who have this surgery will take part in a structured physiotherapy program. The study will examine changes in physical function, pain, walking ability, and independence before surgery, during recovery, and after removal of the external fixator. The results of this study may help improve rehabilitation planning after cosmetic femoral lengthening surgery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable healthy
Started Feb 2026
Shorter than P25 for not_applicable healthy
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2026
CompletedFirst Submitted
Initial submission to the registry
February 4, 2026
CompletedFirst Posted
Study publicly available on registry
February 25, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2026
CompletedFebruary 25, 2026
February 1, 2026
2 months
February 4, 2026
February 19, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Functional Capacity Assessed by the 30-Second Chair Stand Test
The 30-Second Chair Stand Test is used to assess lower extremity functional strength and overall functional capacity. Participants are instructed to stand up and sit down from a standard chair as many times as possible within 30 seconds. A higher number of repetitions indicates better functional capacity.
Preoperative baseline, postoperative 8th week, and 1 week after removal of the external fixator
Secondary Outcomes (1)
Functional Mobility Assessed by the Timed Up and Go Test
Preoperative baseline, postoperative 8th week, and 1 week after removal of the external fixator
Study Arms (1)
Conventional Physiotherapy Group
EXPERIMENTALParticipants assigned to this arm will receive a structured conventional physiotherapy program following cosmetic femoral lengthening surgery performed using the Lengthening Over Nail (LON) technique. The rehabilitation program will be initiated in the early postoperative period and will include active and passive joint mobilization exercises, quadriceps and hamstring stretching, isometric muscle strengthening, neuromuscular electrical stimulation (NMES), cryotherapy, and functional mobilization with assistive devices. Physiotherapy sessions will be conducted five days per week under the supervision of an experienced physiotherapist.
Interventions
Conventional physiotherapy will be administered following cosmetic femoral lengthening surgery performed using the Lengthening Over Nail (LON) technique. The rehabilitation program will begin in the early postoperative period and will be conducted five days per week for a total duration of thirteen weeks. The intervention will include active and passive joint mobilization exercises, quadriceps and hamstring stretching exercises, isometric muscle strengthening, neuromuscular electrical stimulation (NMES), cryotherapy, functional ambulation training with assistive devices such as walkers or crutches, elastic band resistance exercises, and modified apparatus-based Pilates exercises. All sessions will be supervised by an experienced physiotherapist.
Eligibility Criteria
You may qualify if:
- Adults aged between 18 and 45 years.
- Individuals who have undergone cosmetic femoral lengthening surgery using the Lengthening Over Nail (LON) technique.
- Participants who are able to attend and comply with the planned postoperative conventional physiotherapy program.
- Individuals who have provided written informed consent.
You may not qualify if:
- Presence of neuromuscular diseases (e.g., cerebral palsy, muscular dystrophy).
- History of lower extremity surgery other than the femoral lengthening procedure.
- Advanced contractures, deformities, or osteoarthritis of the hip or knee joint.
- Severe psychiatric disorders or cognitive impairment preventing cooperation with the study procedures.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- FATMA ÇAVDARCIlead
Study Sites (1)
Istanbul Aydin University
Istanbul, Kucukcekmece, 34295, Turkey (Türkiye)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- PhD Candidate, Department of Physiotherapy and Rehabilitation
Study Record Dates
First Submitted
February 4, 2026
First Posted
February 25, 2026
Study Start
February 1, 2026
Primary Completion
April 1, 2026
Study Completion
May 1, 2026
Last Updated
February 25, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share
Individual participant data (IPD) will not be shared. The study is a single-center academic research project, and data sharing was not included in the original study protocol or informed consent documents. All collected data will be used solely for the purposes of this research and will be reported only in aggregate form.