Clinical Pilates in Hip Osteoarthritis: A Randomised Controlled Trial
Investigation of the Effectiveness of Clinical Pilates in Hip Osteoarthritis: A Randomised Controlled Trial
1 other identifier
interventional
52
1 country
1
Brief Summary
The aim of this study is to investigate the effect of a clinical Pilates exercise program on reducing symptoms in individuals with hip osteoarthritis. The main questions it aims to answer are:
- Does a clinical Pilates exercise program have an effect on pain, range of motion, physical function, performance, spinal mobility, postural control, disability, self-efficacy, and quality of life in individuals with hip osteoarthritis?
- Does a conventional therapeutic exercise program have an effect on pain, range of motion, physical function, performance, spinal mobility, postural control, disability, self-efficacy, and quality of life in individuals with hip osteoarthritis? Researchers will compare clinical pilates program to conventional therapeutic exercise program to see if exercise works to reducing hip osteoarthritis symptoms. Participants will:
- Take clinical pilates or Conventional Therapeutic Exercise twice a week for 12 weeks
- The patients will be assessed by a blind evaluator both before and after the treatment.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Nov 2024
Shorter than P25 for not_applicable
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
November 30, 2024
CompletedFirst Submitted
Initial submission to the registry
January 7, 2025
CompletedFirst Posted
Study publicly available on registry
January 20, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2025
CompletedMarch 25, 2026
March 1, 2026
6 months
January 7, 2025
March 24, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Pain Intensity
Pain intensity will be evaluated using the Visual Analog Scale (VAS). During the assessment, patients will be asked to mark the degree of pain they feel on a 100-mm horizontal line. The distance from the starting point to the marked point will be measured with a ruler, and the pain intensity will be recorded in millimeters. The VAS, developed by Vas Price et al. (1983), is a validated and reliable tool for determining the perceived intensity of pain. It is simple to administer and widely used in clinical practice.
From enrollment to the end of treatment at 12 weeks
Lumbopelvic Stabilization
Lumbopelvic stabilization will be assessed using the "Stabilizer Pressure Biofeedback Unit". Prior to the measurement, each participant will be instructed in the corset technique for contracting the Transversus Abdominis muscle while lying in a supine position. Participants will be asked to lie on their back with their knees bent (hook-lying position), maintaining a neutral and relaxed spinal alignment. A pressure cell, inflated with air and connected to a stabilizer, will be placed under the lumbar spine. The manometer's baseline pressure will be inflated to 40 mmHg. Participants will then be instructed to contract their Transversus Abdominis muscle using the abdominal corset technique without moving the spine or pelvis and without holding their breath. They will be required to maintain this contraction for 5 seconds. After three practice trials to ensure learning, participants will rest for 30 seconds. The actual measurement will consist of three repetitions of 10 seconds each.
From enrollment to the end of treatment at 12 weeks
Secondary Outcomes (10)
Postural Control:
From enrollment to the end of treatment at 12 weeks
The Active Normal Range of Motion
From enrollment to the end of treatment at 12 weeks
Physical Function
From enrollment to the end of treatment at 12 weeks
Disability
From enrollment to the end of treatment at 12 weeks
Self-Efficacy
From enrollment to the end of treatment at 12 weeks
- +5 more secondary outcomes
Study Arms (2)
Clinical Pilates Group
EXPERIMENTALThe patients participated in a Clinical Pilates program under the supervision of a physiotherapist twice a week for a duration of 12 weeks.
Conventional Therapeutic Exercise Program
EXPERIMENTALThe patients participated in a Conventional Therapeutic Exercise program under the supervision of a physiotherapist twice a week for a duration of 12 weeks.
Interventions
Clinical Pilates Session: Each clinical Pilates movement will have three difficulty levels: beginner, intermediate, and advanced. The progression criteria for increasing difficulty will be determined by the prevention of compensatory movements, the ability to activate target muscles, achieving more controlled movements during exercise, and maintaining a more stable posture. This program will include standard hip-focused as well as full-body clinical Pilates movements.
Eligibility Criteria
You may qualify if:
- Age above 18 years
- Diagnosis of hip osteoarthritis (OA) according to the American College of Rheumatology
- Not on the waiting list for hip replacement surgery
- Willingness to participate in the exercise program
You may not qualify if:
- Symptomatic OA in the knee or big toe
- Presence of other types of arthritis
- History of hip and/or knee prosthesis or fracture
- Use of walking aids
- Regular exercise habit of two or more sessions per week
- Corticosteroid injection into the hip within the past 12 months
- Participation in a physical therapy program for hip pain within the past 3 months
- Severe cardiovascular disorders or other comorbidities that significantly limit daily physical capacity or contraindicate physical exertion
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Atatürk Training and Research Hospital
Izmir, 35360, Turkey (Türkiye)
Related Publications (4)
Rego TAM, Ferreira APL, Villela DW, Shirahige L, Xavier AB, Braz RRS, Guerino MR, Araujo MDGR. Effects of mat Pilates on older adult women with knee osteoarthritis: A randomized controlled trial. J Bodyw Mov Ther. 2023 Jan;33:136-141. doi: 10.1016/j.jbmt.2022.02.007. Epub 2022 Apr 15.
PMID: 36775508RESULTPatti A, Zangla D, Sahin FN, Cataldi S, Lavanco G, Palma A, Fischietti F. Physical exercise and prevention of falls. Effects of a Pilates training method compared with a general physical activity program: A randomized controlled trial. Medicine (Baltimore). 2021 Apr 2;100(13):e25289. doi: 10.1097/MD.0000000000025289.
PMID: 33787615RESULTGebhart JJ, Weinberg DS, Bohl MS, Liu RW. Relationship between pelvic incidence and osteoarthritis of the hip. Bone Joint Res. 2016 Feb;5(2):66-72. doi: 10.1302/2046-3758.52.2000552.
PMID: 26912384RESULTBannuru RR, Osani MC, Vaysbrot EE, Arden NK, Bennell K, Bierma-Zeinstra SMA, Kraus VB, Lohmander LS, Abbott JH, Bhandari M, Blanco FJ, Espinosa R, Haugen IK, Lin J, Mandl LA, Moilanen E, Nakamura N, Snyder-Mackler L, Trojian T, Underwood M, McAlindon TE. OARSI guidelines for the non-surgical management of knee, hip, and polyarticular osteoarthritis. Osteoarthritis Cartilage. 2019 Nov;27(11):1578-1589. doi: 10.1016/j.joca.2019.06.011. Epub 2019 Jul 3.
PMID: 31278997RESULT
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- associate professor
Study Record Dates
First Submitted
January 7, 2025
First Posted
January 20, 2025
Study Start
November 30, 2024
Primary Completion
June 1, 2025
Study Completion
June 1, 2025
Last Updated
March 25, 2026
Record last verified: 2026-03