Clinical trials

19

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Radiographic Cortical Thickness of the Humerus in Detecting Post-Stroke Regional Bone Loss

Post-stroke immobilization and reduced weight-bearing frequently lead to significant regional bone mineral density loss and asymmetry, particularly in the paretic upper extremity, which increases fracture risks. While Dual-Energy X-ray Absorptiometry (DXA) is the gold standard for evaluating systemic bone loss, it primarily focuses on axial or lower extremity sites and lacks universal accessibility. Since routine shoulder radiographs offer an opportunistic screening tool to evaluate regional bone quality without additional radiation , this study aims to compare proximal humerus cortical bone thickness between the paretic and non-paretic sides in stroke patients and assess its correlation with systemic DXA values to determine its clinical utility. This cross-sectional, observational study involves a retrospective data analysis of patients aged 18 and older who experienced a single unilateral stroke at least 6 months prior and present with clinical hemiparesis. Eligible participants must have concurrent standard anteroposterior shoulder radiographs and DXA measurements available from their routine clinical follow-ups. Patient demographic data, stroke characteristics, Brunnstrom stages, and systemic DXA measurements (femoral neck and lumbar spine T-scores and bone mineral density values) are systematically recorded for analysis. Cortical bone thickness measurements are performed using ImageJ software on standard radiographs at points 10 cm and 12 cm distal to the highest point of the humerus. To ensure reliability, measurements for both the paretic and non-paretic sides are conducted independently by two researchers who are completely blinded to the DXA results. Statistical analyses, including paired t-tests or Wilcoxon tests and Pearson or Spearman correlations, will be used to compare the sides and evaluate the relationship between radiographic cortical thickness and systemic bone density.

Participants needed: 65
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: Jun 16, 2026Locations: 1
Eligibility criteria

Patients aged 18 years and older. [+3]

History of surgical intervention in either shoulder. History of a proximal humer... [+5]

Status: Recruiting

Bone Myoregulation Reflex and Postural Control in Vitamin D Deficiency

This observational study aims to investigate the relationship between vitamin D deficiency, postural stability, and neuromuscular control mechanisms in adults. The study will compare individuals with vitamin D deficiency and healthy controls. Participants will undergo a single-session evaluation including surface electromyography and postural stability assessments during standing tasks under different loading and vibration conditions. No invasive procedures, medications, or blood sampling will be performed. Previously obtained routine laboratory results will be used for vitamin D status. The study is designed to improve understanding of neuromuscular responses associated with vitamin D deficiency and to contribute to future rehabilitation strategies.

Participants needed: 24
Trial details
Age: 20-40Biological sex: AllType: ObservationalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: May 27, 2026Locations: 1
Eligibility criteria

Age 20 to 40 years. [+4]

Known metabolic bone disease other than vitamin D deficiency. [+7]

Status: Recruiting

Caregiver Burden in Caregivers of Patients With Multiple Sclerosis

Individuals aged 18-80 years who have been clinically diagnosed with multiple sclerosis and their caregivers will be included in the study. Demographic data of the patients, including age, height, weight, and comorbidities, will be recorded. Disease-specific characteristics such as disease duration, presence of incontinence, ambulation status, and presence and severity of pain will be assessed. Functional status of the patients will be evaluated using the Expanded Disability Status Scale (EDSS) and the Multiple Sclerosis Impact Scale (MSIS). Symptoms related to depression and anxiety in patients will be assessed using the Hospital Anxiety and Depression Scale (HADS). Subsequently, caregivers of the patients will be evaluated. The severity of insomnia will be assessed using the Insomnia Severity Index (ISI). Symptoms related to anxiety and depression will be evaluated using the Hospital Anxiety and Depression Scale (HADS). Caregiver burden will be assessed using the Zarit Caregiver Burden Scale.

Participants needed: 50
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: Apr 23, 2026Locations: 1Duration: 1 Day
Eligibility criteria

Age 18-80 years [+5]

Severe cognitive impairment or communication problems preventing questionnaire c... [+6]

Status: Not yet recruiting

Motor Imagery Reaction Time in Individuals With Paraplegic Spinal Cord Injury

Individuals aged 18-65 years who have been clinically diagnosed with spinal cord injury and have developed paraplegia will be included in the study. Demographic and clinical data of the participants, including age, sex, height, weight, etiology of injury, level of injury, duration of injury, and comorbidities, will be recorded. In addition, disease-specific characteristics such as ambulation status, wheelchair use, presence of incontinence, and presence and severity of pain will be assessed. For the healthy control group, demographic data including age, sex, height, weight, and comorbidities will be recorded. Motor imagery performance of the participants will be evaluated using a computer-based left/right judgment task. In this context, both upper extremity (hand) and lower extremity (foot) images will be used to record reaction time (motor imagery reaction time) and accuracy rate. All tests will be performed under standardized conditions, in a seated position, and using the same device.

Participants needed: 128
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: Apr 23, 2026Locations: 1Duration: 1 Day
Eligibility criteria

Aged between 18 and 65 years [+8]

Tetraplegia [+7]

Status: Not yet recruiting

Kinesiophobia, Fear of Falling, Functional Independence, and Psychological Status in Spinal Cord Injury

Individuals aged 18-65 years who have been clinically diagnosed with spinal cord injury and have developed paraplegia will be included in the study. Demographic and clinical data of the participants, including age, sex, height, weight, etiology of injury, level of injury, duration of injury, and comorbidities, will be recorded. In addition, disease-specific characteristics such as ambulation status, wheelchair use, presence of incontinence, and presence and severity of pain will be assessed. Kinesiophobia levels of the patients will be evaluated using the Tampa Scale for Kinesiophobia (TSK). Functional independence will be assessed using the Spinal Cord Independence Measure-III Self-Report (SCIM-III SR). Fall-related concerns will be evaluated using the Spinal Cord Injury-Falls Concern Scale (SCI-FCS). Pain severity will be assessed using the Visual Analog Scale (VAS), and the presence of neuropathic pain will be evaluated using the DN4 Neuropathic Pain Questionnaire. Symptoms related to anxiety and depression will be assessed using the Hospital Anxiety and Depression Scale (HADS). All assessments will be conducted through face-to-face interviews. The collected data will be analyzed to investigate the relationship between kinesiophobia and functional independence, fear of falling, pain, and psychological status in individuals with paraplegic spinal cord injury. Validated Turkish versions of all scales used in the study will be employed.

Participants needed: 70
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: Apr 24, 2026Duration: 1 Day
Eligibility criteria

Aged between 18 and 65 years [+6]

Tetraplegia or other neurological conditions affecting motor function [+6]

Status: Not yet recruiting

Muscle Strength Asymmetry In Sarkopenic And Non-sarcopenic Older Adults

The purpose of this observational study is to examine whether differences in muscle strength between the dominant and non-dominant sides of the body are associated with sarcopenia in older adults. The study will include adults aged 65 years and older with and without sarcopenia. Muscle strength will be measured on both sides of the body using handgrip strength as well as strength measurements of the biceps (upper arm muscle) and quadriceps (thigh muscle). The difference in strength between the dominant and non-dominant sides will be calculated and compared between participants with sarcopenia and those without sarcopenia. The main question it aims to answers are: * Do older adults with sarcopenia have larger differences in muscle strength between the two sides of the body compared with those without sarcopenia? * Can differences in arm and leg muscle strength help identify older adults who may be at higher risk of sarcopenia?

Participants needed: 140
Trial details
Age: 65+Biological sex: AllType: ObservationalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: Mar 5, 2026Locations: 1
Eligibility criteria

Age 65 years or older [+4]

Lack of cooperation, moderate to severe dementia (e.g., MMSE <24) or conditions... [+5]

Status: Recruiting

The Effect of Virtual Reality Therapy on Upper Extremity Functions in Subacute Stroke Patients Receiving Rehabilitation

Stroke ranks second among the leading causes of death worldwide and third among the causes of disability. In stroke patients, motor impairment typically affects facial movements and the upper and lower extremities unilaterally. Upper extremity involvement, in particular, negatively impacts patients' activities of daily living, such as eating and dressing. Various rehabilitation methods are used to improve the function of the paretic upper extremity in stroke patients. Action Observation Therapy and Virtual Reality are among the rehabilitation approaches currently used to support upper extremity rehabilitation. In our study, patients will be randomly divided into two groups: one group will receive conventional rehabilitation and Action Observation Therapy, while the other group will additionally receive Virtual Reality therapy. This study aims to investigate the contribution of Virtual Reality therapy, when added to conventional rehabilitation and Action Observation Therapy, to the recovery of the paretic upper extremity in patients with subacute stroke.

Participants needed: 38
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: Jan 28, 2026Locations: 1
Eligibility criteria

Patients over the age of 18 [+4]

Presence of pain in the paretic shoulder severe enough to prevent exercise [+6]

Status: Recruiting

Neuropathic Pain in Knee Osteoarthritis: Pain Severity and Functional Status

Osteoarthritis (OA) is a degenerative joint disease characterized by structural changes such as cartilage loss and osteophyte formation, leading to functional limitations and disability. Pain in knee OA involves a complex pathophysiological structure including both nociceptive and neuropathic mechanisms. Identifying the neuropathic pain component is clinically significant for improving quality of life and functional recovery. This cross-sectional controlled clinical study aims to determine the prevalence of neuropathic pain in patients with knee OA and evaluate its impact on pain severity and functional status. Patients will be categorized based on the Douleur Neuropathique 4 (DN4) questionnaire and assessed using various pain and functional scales.

Participants needed: 102
Trial details
Age: 40-70Biological sex: AllType: ObservationalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: Jan 26, 2026Locations: 1
Eligibility criteria

Diagnosed with Knee OA according to ACR criteria. [+2]

History of surgical intervention in the affected knee. [+8]

Status: Recruiting

The Ultrasonographic Evaluation of Abdominal Accessory Respiratory Muscle Thickness in Patients With Parkinson's Disease: Correlation With Disease Severity and Expiratory Respiratory Muscle Strength

Parkinson's disease is a neurodegenerative disorder characterized by both motor and non-motor symptoms. The involvement of respiratory muscles can lead to impairments in respiratory function in these patients. In this study is to evaluate the thickness of abdominal accessory respiratory muscles using ultrasonography in patients with Parkinson's disease. Additionally, the relationship between disease severity and expiratory respiratory muscle strength will be examined. The study will include Parkinson's patients at different stages of the disease, with respiratory muscle thickness measured via ultrasonography. The collected data will then be compared with disease severity and expiratory muscle strength.

Participants needed: 36
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: Jan 2, 2026Locations: 1
Eligibility criteria

Age > 18 years [+3]

Active smokers [+5]

Status: Recruiting

Kinesiophobia and Balance in Stroke Patients

This is a cross-sectional clinical study planned to include 138 stroke patients receiving inpatient treatment at the Istanbul Physical Therapy and Rehabilitation Training and Research Hospital.Data on kinesiophobia (Tampa Kinesiophobia Scale-17) , balance performance (Berg Balance Scale) , balance confidence (Activities-specific Balance Confidence Scale-6) , fear of falling (Falls Efficacy Scale) , pain (VAS) , and mood (HADS) will be collected. Clinical and demographic data, including Brunnstrom stages and Barthel Index, will also be recorded. The relationships between these variables will be analyzed statistically.

Participants needed: 138
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: Nov 28, 2025Locations: 1Duration: 1 Day
Eligibility criteria

Voluntary participation in the study [+5]

History of musculoskeletal surgery within the last year [+5]

Status: Not yet recruiting

Turkish Adaptation, Validity, and Reliability Study of the Patient Experience With Treatment and Self-Management Scale in Stroke

This study will include individuals aged 18-80 years who have been clinically diagnosed with stroke and have spent at least one month at home after discharge. Sociodemographic and clinical characteristics will be recorded. Functional status will be assessed using the Modified Rankin Scale, Brunnstrom Stages, and the Modified Barthel Index. Ambulation status will be documented with the Holden Scale. The scale will first be translated into Turkish and then back-translated into English by a bilingual expert whose native language is English. The Turkish version of the scale will be administered to patients. Two independent evaluators will apply the scale twice, one week apart. Validity will be examined by analyzing the relationship between the scale and the Stroke Impact Scale and the Treatment Burden Questionnaire

Participants needed: 170
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: Nov 28, 2025Locations: 1Duration: 1 Week
Eligibility criteria

Clinical diagnosis of stroke (ischemic or hemorrhagic). [+5]

History of subarachnoid hemorrhage. [+4]

Status: Recruiting

Effect of Mechanical Loading and Bone Loss on Motor Neuron Activity-H-Reflex Relationship

Weight-bearing exercises (e.g., running, jumping, whole-body vibration) are widely practiced due to their beneficial effects on bone development and their role in the prevention and treatment of osteoporosis. However, the underlying neuroregulatory mechanisms responsible for these positive effects have not yet been fully understood. Two main neuromodulatory mechanisms have been proposed in the literature: (i) spinal reflexes originating from muscle spindles (stretch reflex, tonic vibration reflex), and (ii) the bone myoregulation reflex (BMR) based on load-sensitive osteocytes. It is well established that increased voluntary contraction and the associated rise in background EMG activity, that is, motor neuron pool activity, enhance muscle spindle-based reflex responses (such as the H-reflex and tendon reflex). In contrast, it has been demonstrated that the H-reflex is suppressed during bone-loading activities such as single-leg stance, jumping, or whole-body vibration. This study is based on two hypotheses: * As mechanical loading increases, Ia inhibitory effects intensify, leading to greater H-reflex suppression. * During whole-body vibration, the H-reflex is suppressed due to Ia inhibition. If this inhibition originates from load-sensitive receptors-osteocytes-and thus from the BMR, then in osteoporosis, where osteocyte number and function are reduced, H-reflex suppression will be diminished. The aim of this research is to test these hypotheses. Confirmation of these assumptions would suggest that reflex control during weight-bearing exercise occurs predominantly through osteocyte-mediated BMR mechanisms rather than muscle spindle-based mechanisms such as the stretch or tonic vibration reflex.

Participants needed: 24
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: Nov 28, 2025Locations: 1
Eligibility criteria

Being in the postmenopausal period [+3]

Receiving osteoporosis treatment [+7]

Status: Not yet recruiting

The Relationship Between Mood and Insomnia Severity and Caregiver Burden in Caregivers of Stroke

This study will include stroke patients aged 18-80 years and their caregivers. Demographic data such as age, height, weight, and comorbidities will be recorded, along with stroke-specific characteristics including duration of stroke, affected side, lesion location, and etiology. Patients' functional status will be assessed using the Modified Rankin Scale, Brunnstrom Stages, and the Modified Barthel Index, while ambulation status will be documented with the Holden Scale. Caregivers will complete the Insomnia Severity Index to assess the severity of sleep disturbances and the Hospital Anxiety and Depression Scale to evaluate anxiety and depressive symptoms. Caregiver burden will be measured using the Zarit Caregiver Burden Scale. The study aims to investigate the relationship between caregivers' mood, insomnia severity, and caregiver burden.

Participants needed: 100
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: Nov 28, 2025Locations: 1Duration: 1 Day
Eligibility criteria

Age 18-80 years. [+4]

History of subarachnoid hemorrhage. [+3]

Status: Recruiting

Botulinum Toxin Applications in Hemiplegic Patients

This retrospective study will be conducted by reviewing the medical records of hemiplegic patients who received botulinum toxin treatment between 2017 and 2020 at the Physical Medicine and Rehabilitation outpatient clinic of Istanbul Physical Medicine and Rehabilitation Training and Research Hospital. A total of 35 hemiplegic patients who underwent botulinum toxin injection and had at least two follow-up records (with a 6-month interval) will be included. Sociodemographic and clinical data, stroke-related characteristics, botulinum toxin dosage, injected muscle groups, medications, and comorbidities will be recorded. Functional assessments, including the Functional Independence Measure (FIM) and Brunnstrom stage, as well as spasticity evaluations using the Modified Ashworth Scale and the Global Spasticity Index, will be obtained from patient files.

Participants needed: 34
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: Nov 20, 2025Locations: 1
Eligibility criteria

Aged between 18 and 75 years, clinically diagnosed with hemiplegia [+3]

Missing essential data (e.g., absence of FIM, MAS, GSI, or GAS at either visit) [+2]

Status: Not yet recruiting

Pain and Fascia Thickness After Steroid Injection in Plantar Fasciitis

The aim of this study is to evaluate the effects of local corticosteroid injection on pain, foot function index, and plantar fascia thickness in patients clinically diagnosed with plantar fasciitis, and to determine whether local corticosteroid injection is an appropriate treatment option for plantar fasciitis. For this purpose, the study plans to assess plantar fascia thickness using ultrasonography, evaluate pain using the Visual Analog Scale (VAS), and investigate the impact on daily living activities in patients who have been clinically diagnosed with plantar fasciitis and treated with local corticosteroid injections.

Participants needed: 33
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: Jul 18, 2025Locations: 1
Eligibility criteria

Patients who were clinically diagnosed with plantar fasciitis and received corti...

Pregnancy [+4]

Status: Recruiting

Effect of Kinesiology Taping and Swallowing Exercises on Suprahyoid Muscle Thickness and Swallowing Function in Stroke Patients With Dysphagia

This randomized controlled single-blind study aims to investigate the effect of kinesiology taping combined with resistance exercises on suprahyoid muscle thickness and swallowing function in patients with stroke-related dysphagia. A total of 36 participants will be randomly assigned to an intervention group receiving real kinesiology taping and a control group receiving placebo taping, both combined with standardized swallowing exercises for 6 weeks. Outcome measures include ultrasonographic evaluation of oropharyngeal muscles (geniohyoid, mylohyoid, anterior digastric, and tongue muscles), swallowing function assessed by the Volume-Viscosity Swallow Test, EAT-10, T-SWAL-QOL, Dysphagia Handicap Index, FOIS, and Functional Ambulation Level. This study will contribute to determining effective rehabilitation methods for improving safe swallowing in post-stroke patients.

Participants needed: 36
Trial details
Age: 50-80Biological sex: AllType: InterventionalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: May 30, 2025Locations: 1
Eligibility criteria

Patients aged between 50 and 80 years [+3]

Open wounds or unresolved skin problems in the neck area [+3]

Status: Recruiting

Ultrasound Assessment of Neck Muscles and Balance in Male Patients With Ankylosing Spondylitis

The aim of this study is to evaluate the relationship between ultrasonographic measurements of the cervical muscles and balance parameters in patients diagnosed with ankylosing spondylitis (AS)

Participants needed: 76
Trial details
Age: 18-65Biological sex: MaleType: ObservationalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: May 13, 2025Locations: 1
Eligibility criteria

Age between 18 and 65 years. [+2]

Orthopedic disorders affecting the spine or lower limbs. [+7]

Status: Recruiting

Turkish Validity and Reliability of the Expanded Rehabilitation Complexity Scale

The RCS is a tool that can assess the need for complex rehabilitation and objectively indicate that a patient may have difficulty functioning well at home or in the community if their medical needs are still high. Among rehabilitation patients, there are still patients with complex needs, even though they have maximized rehabilitation potential. Moreover, RCS can also be useful in highlighting cases of patients becoming seriously ill during the rehabilitation process due to an acute illness such as sepsis, which significantly limits treatment time. This information can be emphasized using RCS data when requesting extended or increased rehabilitation support.

Participants needed: 110
Trial details
Age: 2-6Biological sex: AllType: ObservationalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: Nov 8, 2024Locations: 1Duration: 2 Months
Eligibility criteria

Not listed

Status: Not yet recruiting

Mimic Muscle Volume, Central Facial Palsy Severity and Dysphagia

70 stroke patients with central facial paralysis will be included and their demographic data will be questioned and facial nerve thickness, depressor labi inferior, depressor anguli oris, buccinator and risorius muscles will be evaluated.

Participants needed: 70
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: Sep 26, 2024
Eligibility criteria

Diagnosis of stroke and presence of unilateral central facial paralysis, [+3]

Presence of previous facial paralysis or a neurological disease other than strok... [+5]