Hip Injuries and DisordersNCT06851793
Investigating Postural Parameters in Different Hip Pathologies
An observational study of Hip Injuries and Disorders, run by Hacettepe University at 1 site in Turkey (Türkiye).
Trial summary
"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. Read more about this study
- Who is it for?
- Ages 18 to 65 yearsHealthy volunteers can take part
- Conditions the study is for
- Hip Injuries and Disorders
- How many people
- 110 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 2 Oct 2025to 11 Dec 2025
- How long will I take part?
- 1 Day
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Individuals with different hip pathologies (hip osteoarthritis, hip impingement syndrome, hip labrum tear, hip dysplasia, hip avascular necrosis) who volunteered the participate the study
Who may be able to join
- 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
Who cannot join
- 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 locations and contacts
1 site in 1 country.
About this study
Official title: Investigation of Postural Parameters, Physical Functions, Balance and Quality of Life in Different Hip Pathologies
"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."
Read the detailed 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.
- Conditions
- Hip Injuries and Disorders
- Keywords
- Hip Injuries and Disorders, Posture, Hip Functions, Physical Function, Pelvis
- Medical subject headings
- Hip Injuries, Disease
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Individuals with hip pathologies | 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 | 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. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Postural Parameter
The postures of the participants will be evaluated using the 4-DIERS. In this method, white light lines (raster lines) are projected onto the participants' backs, and the curvature of these lines is used to create a 3D shape of the back. The patterns formed by these curved lines are detected by the camera. With the help of the software, the detected convex and concave regions allow for the immediate determination of anatomical landmarks and fixed points. A mathematical algorithm is used to reconstruct a three-dimensional model of the spine.
Measured: Up to 4 weeks
Secondary outcomes (5)
Pain Threshold
The pain threshold evaluation with an algometer is a method used to assess an individual's sensitivity to pressure-induced pain. An algometer is a device that applies gradually increasing pressure to a specific point on the body until the subject perceives pain. This measurement is referred to as the pressure pain threshold (PPT) and is widely used in clinical and research settings to evaluate pain sensitivity in conditions such as musculoskeletal disorders, fibromyalgia, and chronic pain syndromes.
Pain threshold values are typically recorded in kilograms per square centimeter (kg/cm²) or Newtons (N). The minimum pain threshold represents the lowest pressure at which pain is first perceived, while the maximum pain threshold indicates the highest tolerated pressure before withdrawal. The mean PPT is calculated based on multiple measurements at different anatomical sites to provide a more reliable assessment of an individual's pain sensitivity. Lower pain threshold values suggest high
Measured: Baseline
Hip and Hip Related Pain
The Visual Analog Scale (VAS) is a widely used tool for assessing pain intensity and other subjective experiences, such as fatigue or discomfort. It consists of a 10-centimeter (100 mm) horizontal or vertical line, with endpoints representing "no pain" (0) on the left and "worst imaginable pain" (10 or 100) on the right. Patients mark a point on the line that best reflects their perceived pain intensity.
The minimum VAS score is 0, indicating no pain, while the maximum score is 10 (or 100, depending on scaling), representing severe or unbearable pain. The mean VAS score is often calculated in studies to determine the average pain level within a group of patients. The scale is simple, quick to administer, and highly effective in capturing pain variations over time, making it a valuable tool in clinical practice and research for monitoring pain management and treatment outcomes.
Measured: Baseline
Muscle Strength
The Lafayette Manual Muscle Dynamometer (Lafayette MMD) is a handheld device used to measure muscle strength in various muscle groups. It provides objective, quantifiable data on muscle force production, making it useful in rehabilitation, sports science, and clinical assessments of neuromuscular conditions. The device applies resistance to a specific muscle or muscle group while recording the maximum isometric force exerted by the patient.
Muscle strength measurements with the Lafayette MMD are typically recorded in kilograms (kg) or Newtons (N). The minimum strength value represents the lowest recorded force, while the maximum strength value is the highest force exerted by the muscle during testing. The mean strength value is calculated to provide an overall assessment of muscle function. Higher values indicate greater muscle strength, whereas lower values may suggest muscle weakness or impairment, which is particularly relevant for patients undergoing rehabilitation or recovering
Measured: Baseline
Hip Functions
The Harris Hip Score (HHS) is a clinician-based outcome measure used to assess the function, pain, and range of motion in patients undergoing hip surgery or suffering from hip disorders. The total score ranges from 0 to 100, with higher scores indicating better hip function. The HHS includes four main components: pain (44 points), function (47 points), absence of deformity (4 points), and range of motion (5 points). A score of 90-100 is considered excellent, 80-89 good, 70-79 fair, and below 70 poor.
Measured: Baseline
Hip Functions
The Hip Outcome Score (HOS) is a patient-reported outcome measure designed primarily for younger, active individuals, especially those undergoing hip arthroscopy. It consists of two subscales: the Activities of Daily Living (ADL) subscale (17 items) and the Sports subscale (9 items). Each item is scored on a 0 to 4 scale, with 0 representing an inability to perform the activity and 4 indicating no difficulty. The total score is calculated as a percentage, with 100% representing the best possible function. The HOS is particularly useful for assessing hip function in active populations and tracking progress after surgical or non-surgical interventions.
Measured: Baseline
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Feb 2025
- Study start2 Oct 2025
- Primary completion10 Nov 2025
- Study completion11 Dec 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (11)Papers the sponsor has linked to this study.
- Other trials for Hip Injuries and DisordersStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case-control
- Time perspective
- Prospective
- Enrolment
- 110 participants (actual)
- Target duration
- 1 Day
Sponsor and investigators
- Lead sponsor
- Hacettepe University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Esra ATEŞ NUMANOĞLU, Hacettepe University
- Investigators
- Melike Naz GÜREL, MSc, Study chair, Hacettepe UniversityGürsoy COŞKUN, Prof, Study chair, Hacettepe UniversityEsra ATEŞ NUMANOĞLU, PhD, Principal investigator, Hacettepe UniversityAsude ARIK, PhD, Study chair, Hacettepe University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06851793
- Sponsor's protocol ID
- SBA 24/191
- Status last verified
- Dec 2025
- First submitted
- 28 Oct 2024
- Last updated
- 18 Dec 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Kechagias VA, Grivas TB, Papagelopoulos PJ, Kontogeorgakos VA, Vlasis K. Truncal Changes in Patients Suffering Severe Hip or Knee Osteoarthritis: A Surface Topography Study. Clin Orthop Surg. 2021 Jun;13(2):185-195. doi: 10.4055/cios20123. Epub 2021 Mar 16.
PubMed 34094009Jain M, Mohapatra A, Tripathy SK, Mohakud S, Das A, Sethy SS. Do Spinopelvic Parameters Relate with Secondary Hip Spine Syndrome in Secondary Hip Arthritis? Indian J Orthop. 2022 Sep 10;56(11):1937-1943. doi: 10.1007/s43465-022-00741-1. eCollection 2022 Nov.
PubMed 36310546Lanza MB, Arbuco B, Ryan AS, Shipper AG, Gray VL, Addison O. Systematic Review of the Importance of Hip Muscle Strength, Activation, and Structure in Balance and Mobility Tasks. Arch Phys Med Rehabil. 2022 Aug;103(8):1651-1662. doi: 10.1016/j.apmr.2021.12.008. Epub 2022 Jan 5.
PubMed 34998714Degenhardt BF, Starks Z, Bhatia S. Reliability of the DIERS Formetric 4D Spine Shape Parameters in Adults without Postural Deformities. Biomed Res Int. 2020 Feb 13;2020:1796247. doi: 10.1155/2020/1796247. eCollection 2020.
PubMed 32104678Mayne E, Memarzadeh A, Raut P, Arora A, Khanduja V. Measuring hip muscle strength in patients with femoroacetabular impingement and other hip pathologies: A systematic review. Bone Joint Res. 2017 Jan;6(1):66-72. doi: 10.1302/2046-3758.61.BJR-2016-0081.
PubMed 28108483Philippi MT, Kahn TL, Adeyemi TF, Maak TG, Aoki SK. Leg dominance as a risk factor for femoroacetabular impingement syndrome. J Hip Preserv Surg. 2020 Feb 13;7(1):22-26. doi: 10.1093/jhps/hnaa007. eCollection 2020 Jan.
PubMed 32382425Euasobhon P, Atisook R, Bumrungchatudom K, Zinboonyahgoon N, Saisavoey N, Jensen MP. Reliability and responsivity of pain intensity scales in individuals with chronic pain. Pain. 2022 Dec 1;163(12):e1184-e1191. doi: 10.1097/j.pain.0000000000002692. Epub 2022 May 18.
PubMed 35584261Kinser AM, Sands WA, Stone MH. Reliability and validity of a pressure algometer. J Strength Cond Res. 2009 Jan;23(1):312-4. doi: 10.1519/jsc.0b013e31818f051c.
PubMed 19130648Romero-Franco N, Jimenez-Reyes P, Montano-Munuera JA. Validity and reliability of a low-cost digital dynamometer for measuring isometric strength of lower limb. J Sports Sci. 2017 Nov;35(22):2179-2184. doi: 10.1080/02640414.2016.1260152. Epub 2016 Nov 24.
PubMed 27882825Polat G, Celik D, Cil H, Erdil M, Asik M. Evidence for reliability, validity and responsiveness of Turkish version of Hip Outcome Score. Acta Orthop Traumatol Turc. 2017 Jul;51(4):319-324. doi: 10.1016/j.aott.2017.05.001. Epub 2017 Jun 9.
PubMed 28602527Celik D, Can C, Aslan Y, Ceylan HH, Bilsel K, Ozdincler AR. Translation, cross-cultural adaptation, and validation of the Turkish version of the Harris Hip Score. Hip Int. 2014 Sep-Oct;24(5):473-9. doi: 10.5301/hipint.5000146. Epub 2014 Sep 10.
PubMed 25264204
Study at a glance
From the registry record, last updated by the sponsor on 18 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Investigation of Postural Parameters, Physical Functions, Balance and Quality of Life in Different Hip Pathologies
- ClinicalTrials.gov ID
- NCT06851793
- Acronym / sponsor ID
- SBA 24/191
- Conditions
- Hip Injuries and Disorders
- Keywords
- Hip Injuries and Disorders, Posture, Hip Functions, Physical Function, Pelvis
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 110 participants (actual)
- Lead sponsor
- Hacettepe UniversityUniversity, hospital or other
- Study start
- 2 Oct 2025 (actual)
- Primary completion
- 10 Nov 2025 (actual)
- Study completion
- 11 Dec 2025 (actual)
- First posted
- 28 Feb 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
"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."
Detailed 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.
Study design
- Observational model
- Case-control
- Time perspective
- Prospective
- Target follow-up
- 1 Day
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Individuals with hip pathologies | – | –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 | – | –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. |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Individuals with different hip pathologies (hip osteoarthritis, hip impingement syndrome, hip labrum tear, hip dysplasia, hip avascular necrosis) who volunteered the participate the study
Key inclusion criteria (4 listed)
- 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
Key exclusion criteria (7 listed)
- 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,
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Postural Parameter
Time frame: Up to 4 weeks
The postures of the participants will be evaluated using the 4-DIERS. In this method, white light lines (raster lines) are projected onto the participants' backs, and the curvature of these lines is used to create a 3D shape of the back. The patterns formed by these curved lines are detected by the camera. With the help of the software, the detected convex and concave regions allow for the immediate determination of anatomical landmarks and fixed points. A mathematical algorithm is used to reconstruct a three-dimensional model of the spine.
5 secondary outcomes
Pain Threshold
Time frame: Baseline
Hip and Hip Related Pain
Time frame: Baseline
Muscle Strength
Time frame: Baseline
Hip Functions
Time frame: Baseline
Hip Functions
Time frame: Baseline
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Dec 2025.
- Background: PubMed 34094009Kechagias VA, Grivas TB, Papagelopoulos PJ, Kontogeorgakos VA, Vlasis K. Truncal Changes in Patients Suffering Severe Hip or Knee Osteoarthritis: A Surface Topography Study. Clin Orthop Surg. 2021 Jun;13(2):185-195. doi: 10.4055/cios20123. Epub 2021 Mar 16.
- Background: PubMed 36310546Jain M, Mohapatra A, Tripathy SK, Mohakud S, Das A, Sethy SS. Do Spinopelvic Parameters Relate with Secondary Hip Spine Syndrome in Secondary Hip Arthritis? Indian J Orthop. 2022 Sep 10;56(11):1937-1943. doi: 10.1007/s43465-022-00741-1. eCollection 2022 Nov.
- Background: PubMed 34998714Lanza MB, Arbuco B, Ryan AS, Shipper AG, Gray VL, Addison O. Systematic Review of the Importance of Hip Muscle Strength, Activation, and Structure in Balance and Mobility Tasks. Arch Phys Med Rehabil. 2022 Aug;103(8):1651-1662. doi: 10.1016/j.apmr.2021.12.008. Epub 2022 Jan 5.
- Background: PubMed 32104678Degenhardt BF, Starks Z, Bhatia S. Reliability of the DIERS Formetric 4D Spine Shape Parameters in Adults without Postural Deformities. Biomed Res Int. 2020 Feb 13;2020:1796247. doi: 10.1155/2020/1796247. eCollection 2020.
- Background: PubMed 28108483Mayne E, Memarzadeh A, Raut P, Arora A, Khanduja V. Measuring hip muscle strength in patients with femoroacetabular impingement and other hip pathologies: A systematic review. Bone Joint Res. 2017 Jan;6(1):66-72. doi: 10.1302/2046-3758.61.BJR-2016-0081.
- Background: PubMed 32382425Philippi MT, Kahn TL, Adeyemi TF, Maak TG, Aoki SK. Leg dominance as a risk factor for femoroacetabular impingement syndrome. J Hip Preserv Surg. 2020 Feb 13;7(1):22-26. doi: 10.1093/jhps/hnaa007. eCollection 2020 Jan.
- Background: PubMed 35584261Euasobhon P, Atisook R, Bumrungchatudom K, Zinboonyahgoon N, Saisavoey N, Jensen MP. Reliability and responsivity of pain intensity scales in individuals with chronic pain. Pain. 2022 Dec 1;163(12):e1184-e1191. doi: 10.1097/j.pain.0000000000002692. Epub 2022 May 18.
- Background: PubMed 19130648Kinser AM, Sands WA, Stone MH. Reliability and validity of a pressure algometer. J Strength Cond Res. 2009 Jan;23(1):312-4. doi: 10.1519/jsc.0b013e31818f051c.
- Background: PubMed 27882825Romero-Franco N, Jimenez-Reyes P, Montano-Munuera JA. Validity and reliability of a low-cost digital dynamometer for measuring isometric strength of lower limb. J Sports Sci. 2017 Nov;35(22):2179-2184. doi: 10.1080/02640414.2016.1260152. Epub 2016 Nov 24.
- Background: PubMed 28602527Polat G, Celik D, Cil H, Erdil M, Asik M. Evidence for reliability, validity and responsiveness of Turkish version of Hip Outcome Score. Acta Orthop Traumatol Turc. 2017 Jul;51(4):319-324. doi: 10.1016/j.aott.2017.05.001. Epub 2017 Jun 9.
- Background: PubMed 25264204Celik D, Can C, Aslan Y, Ceylan HH, Bilsel K, Ozdincler AR. Translation, cross-cultural adaptation, and validation of the Turkish version of the Harris Hip Score. Hip Int. 2014 Sep-Oct;24(5):473-9. doi: 10.5301/hipint.5000146. Epub 2014 Sep 10.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Melike Naz GÜREL, MSc study chair
Hacettepe University
Gürsoy COŞKUN, Prof study chair
Hacettepe University
Esra ATEŞ NUMANOĞLU, PhD principal investigator
Hacettepe University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Hip Injuries and Disorders, run by Hacettepe University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 18 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Postural Parameter (time frame: Up to 4 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06851793, which also lists 11 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Dec 2025.