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Pes Planus clinical trials

View clinical trials related to Pes Planus.

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NCT ID: NCT05170698 Completed - Pes Planus Clinical Trials

Management of Pes Planovalgus With Talocalcaneal Coalition ,Osteotomy vs Arthroereisis

Start date: November 18, 2018
Phase: N/A
Study type: Interventional

the investigators compare the corrective osteotomies vs arthroereisis in management of talcalcaneal coalition in adolescents as regard the outcome to provide the best intervention for the patient

NCT ID: NCT05012488 Completed - Pes Planus Clinical Trials

Comparison of the Effects of Morton's Neuroma on Foot Pressure Distribution and Gait Parameters in Pes Planus and Pes Cavus Patients

Start date: July 1, 2021
Phase:
Study type: Observational

The aim of our study is to compare the effect of Morton's neuroma in feet with pes planus and pes cavus on foot pressure and temporal and spatial gait parameters.

NCT ID: NCT04810715 Completed - Clinical trials for Spondylitis, Ankylosing

Frequency of Pes Planus and Posterior Tibial Tendon Dysfunction in Patients With Ankylosing Spondylitis

Start date: March 1, 2021
Phase:
Study type: Observational

This investigation aims to investigate the frequency of pes planus and posterior tibial tendon dysfunction in patients with ankylosing spondylitis.

NCT ID: NCT04734899 Active, not recruiting - Pes Planus Clinical Trials

Foot Core Training in Individuals With Pes Planus

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

Foot core training is very important for the intrinsic muscles of the foot, but it is often neglected in exercise programs given to individuals with pes planus. The aim of our study is to reveal the effects of foot core training, which will be added to the exercise program routinely given to individuals with asymptomatic flexible pes planus, on walking, muscular activations, balance and lower extremity functional performance with objective, evidence based results.

NCT ID: NCT04179591 Completed - Pes Planus Clinical Trials

Effects of Exercise and Insole on Foot Posture, Plantar Force Distribution, and Balance in Individuals With Pes Planus

Start date: November 30, 2019
Phase: N/A
Study type: Interventional

The aim is to compare the effects of intrinsic foot muscles and tibialis posterior strengthening exercise, and customized arch support insoles on foot posture, plantar force distribution, and balance in individuals with flexible pes planus.

NCT ID: NCT04104555 Completed - Pes Planus Clinical Trials

Orthotics for Treatment of Symptomatic Flat Feet in Children

OSTRICH
Start date: April 21, 2022
Phase: N/A
Study type: Interventional

Update 13.12.2021 To mitigate the effects the COVID-19 pandemic, and due to difficulties in sites setting up the custom orthoses arm of the protocol an amendment was approved to change the design of the study from a 3 to a 2 arm trial. The amendment drops the custom orthoses arm and was implemented prior to the start of recruitment. As a child grows the shape of their foot changes and most develop an arch in their foot. For some, however, the arch does not fully form or it might be flat against the ground. This is known as having flat feet and it can cause pain in the feet, legs, or back. At the moment, we are not sure what the best treatment for flat feet is, so the purpose of this research is to conduct a trial to compare two of the most common treatments. The first is exercise and advice about things like which types of shoes might help. The second of the treatment is a type of insole, which is put inside the shoe. Participants will receive their treatment as part of their normal National Health System care. We would like 478 children and young people aged between 6 and 14 years old to take part in the study. Everyone will receive advice about the type of shoes to wear, ankle exercises and things to look out for when children have painful flat feet. In addition to this, half of the participants will receive a pre-made insole that is the right size. We will ask for their help for 12 months. During this time, we will track their progress by sending them 3 questionnaires in the post to fill in and weekly text messages to find out how painful their feet are during the first few months. We also want to learn more about the problems that flat feet cause, and children's experiences of the treatments delivered as part of this clinical trial. We will explore this through in-depth conversations with children and their parent(s) or the person who looks after them. Once we have finished the trial, we will work with the people who took part in the trial, and clinicians, to make sure that our results can be used by as many people as possible. We will run 3 additional studies. The first will find out if having information about the study in the form of a video in addition to information in a paper booklet will increase recruitment rates. The second will find out if sending participants a birthday card will increase the response rates to postal questionnaires. The third study will take a 3D impression of the participant's foot and see if it changes over the course of the study.

NCT ID: NCT03629938 Completed - Pes Planus Clinical Trials

Evaluation and Classification of Foot Medial Longitudinal Arch Height in Adults

Start date: March 3, 2019
Phase:
Study type: Observational [Patient Registry]

The aim of the study is, to evaluate and classificate the medial longitudinal arch height in adult individuals. Aged between 18-40 years,350 adults who are voluntarily participate is going to be evaluate with Feiss Line(FL), Navicular Drop(ND) and Longitudinal Arch Angle(LAA) in subtalar neutral and resting position. Maximum, minimum values are going to be calculated. The 95% and 68% prediction intervals will be used as cut off limits.

NCT ID: NCT03494374 Recruiting - Pes Planus Clinical Trials

The Effect of Orthosis and Exercise in Pes Planus

Start date: December 29, 2016
Phase: N/A
Study type: Interventional

There is no definite evidence for the conservative treatment of pes planus. We want to verify the combination efficacy of orthosis and toe walking exercise for the treatment of pes planus.

NCT ID: NCT03151538 Completed - Pes Planus Clinical Trials

Effects on Pes Planus Exercise Training Mixed With Play on Pre-school Children

Start date: April 19, 2017
Phase: N/A
Study type: Interventional

The study was planned to assess effects on pes planus and femoral anteversion angle of exercise training mixed with play on pre-school children.

NCT ID: NCT02075853 Completed - Cerebral Palsy Clinical Trials

Outcomes of the Evans Calcaneal Lengthening Based on Bone Grafting Material

Start date: September 2010
Phase:
Study type: Observational

The Evans calcaneal lengthening is a common surgical correction used for children with spastic cerebral palsy (CP) and painful flat feet. This procedure involves the insertion of a trapezoidal bone graft into the calcaneus bone. Both autograft and allografting materials have been used for this procedure, but both types of grafting materials have associated limitations. Autologous grafting materials, which are harvested from the iliac crest at the time of surgery, are associated with high rates of prolonged donor site pain. There is limited bone available from the iliac crest. For this reason autologous bone grafts are not commonly used for the Evan's procedure. Cadaver allografting materials are variable in their mechanical and geometric properties. Recently, xenografting materials have been developed that have consistent mechanical properties and are available in a larger size that is formed to fit the individual patient intraoperatively. The purpose of this study is to evaluate the long term outcomes of the procedure with the different graft options. Another purpose is to compare the difference in surgical correction obtained with the cadaver allograft and the xenografting materials. This study will also observe and evaluate a wide range of outcome variables that encompass multiple levels of patient care, from clinical observation to parent and patient satisfaction, and compare these with the observed changes in the radiographic and plantar pressure parameters of the foot. This data will be evaluated pre to post surgery and for two years of follow-up time. The aim is to uncover the characteristics of collapse observed with the two different grafting materials.