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Investigating Postural Parameters in Different Hip Pathologies

H

Hacettepe University

Status

Completed

Conditions

Hip Injuries and Disorders

Study type

Observational

Funder types

Other

Identifiers

NCT06851793
SBA 24/191

Details and patient eligibility

About

"It is known that pelvic parameters affect physical hip functions in hip pathologies. Depending on the type and severity of hip pathologies, posture, muscle strength, balance, and pain parameters may change, thereby impacting an individual's quality of life. This study aimed to examine the postural parameters, muscle strength, balance, quality of life, pain intensity, and pain localization of individuals with different hip pathologies, including hip osteoarthritis, hip impingement syndrome, hip labrum tear, hip dysplasia, and hip avascular necrosis."

Full description

Volunteers with hip pathologies, such as hip osteoarthritis, hip impingement syndrome, hip labrum tear, hip dysplasia, and hip avascular necrosis, will be included in the study. Prior to the study, the responsible researcher will provide detailed face-to-face information regarding the study's content, the scales to be applied, the importance of these scales, and the evaluation processes. Individuals who agree to participate will sign an informed consent form before the evaluations begin. Demographic information will be recorded, and the dominant extremity for both the upper and lower extremities will be determined.

The measurements and evaluations will be conducted by the same researcher using a consistent evaluation method for all participants included in the study.

Volunteers with hip joint pathologies who apply to the Orthopedic Unit of Hacettepe University Faculty of Physical Therapy will be included in the study. During the initial interview, participants will be informed about the surveys and the parameters to be evaluated. The sample size was calculated using the G*Power 3.1 program, with an effect size of 0.74, an alpha error rate of 0.05, and a test power of 0.80. This included individuals with various hip pathologies (hip osteoarthritis, hip impingement syndrome, hip labrum tear, hip dysplasia, and hip avascular necrosis). The sample size for the study was determined to be 30 individuals with hip pathologies and 30 healthy individuals. To account for potential incomplete evaluations, a total of 66 participants, with an additional 10%, will be included.

Inclusion Criteria:

Diagnosed with one of the following: hip osteoarthritis, hip impingement syndrome, hip labrum tear, hip dysplasia, or hip avascular necrosis, experiencing mechanical impact on the hip joint, symptoms ongoing for at least 6 months, aged between 18 and 65 years

Exclusion Criteria:

Diagnosed with scoliosis by a physician, diagnosed with any developmental disorder (e.g., Scheuermann's/Calve disorder), diagnosed with a neurological and/or cognitive disease that may affect cognitive functions, diagnosed with inflammatory arthritis, underwent surgery on the spine or extremities, diagnosed with an infection (e.g., spinal tuberculosis) or tumor (e.g., multiple myeloma), epilepsy or use of antidepressants/attention-enhancing drugs.

Enrollment

110 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Being diagnosed with any of the following: hip osteoarthritis, hip impingement syndrome, hip labrum tear, hip dysplasia, hip avascular necrosis.
  • Having mechanical impact on the hip joint
  • Symptoms have been ongoing for at least 6 months
  • Being between the ages of 18-65

Exclusion criteria

  • Being diagnosed with scoliosis by a physician
  • Being diagnosed with any developmental disorder (Scheuermann's/Calve Disorder etc.),
  • Being diagnosed with a neurological and/or cognitive disease that may affect cognitive functions
  • Being diagnosed with Inflammatory Arthritis
  • Having undergone surgery on the spine and extremities,
  • Getting diagnosed with Infection (Spinal Tuberculosis etc.), Tumor (Multiple Myeloma)
  • Epilepsy, Antidepressant / Attention enhancing drug use

Trial design

110 participants in 2 patient groups

Individuals with hip pathologies
Description:
Volunteers with hip pathology (hip osteoarthritis, hip impingement syndrome, hip labrum tear, hip dysplasia, hip avascular necrosis) who apply to the Orthopedic Rehabilitation Unit of the Faculty of Physical Therapy will be included in this group
Healthy individuals
Description:
Healthy individuals between the ages of 18-65 who have been diagnosed with any of the following diagnoses: hip osteoarthritis, hip impingement syndrome, hip labrum tear, hip dysplasia, or hip avascular necrosis will be included in this group.

Trial contacts and locations

1

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Central trial contact

Esra ATEŞ NUMANOĞLU, PhD; Asude ARIK, PhD

Data sourced from clinicaltrials.gov

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