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The Investigation of the Effects of Physical Therapy and Rehabilitation Applications on the Hip and Defined Functional Parameters in Children With Developmental Hip Dysplasia

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What is being tested

Physical Therapy and Rehabilitation Modalities

+ Conventional Group

Behavioral
Who is being recruted

Congenital Abnormalities+8

+ Developmental Dysplasia of the Hip

+ Behavior

From 2 to 5 Years
+12 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
Study Start: September 2023
See protocol details

Summary

Principal SponsorInonu University
Study ContactElisa Çalışgan, PhDMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: September 1, 2023

Actual date on which the first participant was enrolled.

Developmental dysplasia of the hip (DDH) is a condition that can lead to disability in children and often results in the need for hip replacement surgery at a younger age. In infants older than one year, treatment becomes challenging due to issues like tight soft tissues around the joint and bone structure problems. This study focuses on children aged 2 to 5 years with DDH and examines how physical therapy and rehabilitation can improve hip function and strength. By understanding the impact of these therapies, the study aims to enhance treatment strategies and improve the quality of life for affected children. Participants in the study will undergo physical therapy designed to strengthen the muscles around the hip and improve joint function. Researchers will measure changes in muscle strength and hip stability by looking at specific angles and tension in the hip region. Although there are no specific risks mentioned, the study aims to provide insights that could lead to better management of DDH through non-surgical means, potentially reducing the need for more invasive procedures like surgery.

Official TitleThe Investigation of the Effects of Physical Therapy and Rehabilitation Applications on the Hip and Defined Functional Parameters in Children With Developmental Hip Dysplasia
NCT06007833
Principal SponsorInonu University
Study ContactElisa Çalışgan, PhDMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

30 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 2 to 5 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Congenital AbnormalitiesDevelopmental Dysplasia of the HipBehaviorJoint DislocationsHip DislocationJoint DiseasesMotor ActivityMusculoskeletal AbnormalitiesMusculoskeletal DiseasesCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesWounds and Injuries

Criteria

6 inclusion criteria required to participate
2-5 years old,

Diagnosed with developmental hip dysplasia,

Have not undergone any foot surgery,

Not having any neurological or rheumatological disease,

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6 exclusion criteria prevent from participating
Having neurological problems,

Meningomyelocele (diagnosed with Spina Bifida),

Mental retardation and uncooperative,

Children with inflammation, spasticity, spina bifida, arthrocentesis,

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Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Orthoses and positioning will be applied to the experimental group as a conservative treatment, following post-surgical plastering. In addition, they will receive a physical therapy and rehabilitation program

Group II

Active Comparator
As a conservative treatment in the control group, post-surgical plastering followed by orthoses and positioning will be applied

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Inonu University

Malatya, Turkey (Türkiye)Open Inonu University in Google Maps
SuspendedOne Study Center