Clinical trials

40

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

Condition / disease
Location
Status: Recruiting

The Effect of Internal- or External-Focused Exercise Training, Administered in Conjunction With a Cognitive Task, on Walking, Balance, and Cognitive Functions in Individuals With Multiple Sclerosis

This interventional clinical trial aims to investigate the effects of internal and external focus-based exercise training combined with cognitive dual-task training in individuals diagnosed with multiple sclerosis. The primary objective is to determine whether these exercise approaches improve gait, balance, and cognitive functions. The main research questions are: Does dual-task training combined with internal focus-based exercises improve gait, balance, and cognitive performance? Does dual-task training combined with external focus-based exercises lead to greater improvements compared to internal focus strategies? Participants will be divided into two groups, and the researchers will compare the effects of internal focus-based and external focus-based dual-task exercise training on functional outcomes. Participants will: Perform structured exercise sessions under the supervision of a physiotherapist Engage in dual-task activities by combining motor exercises with simple cognitive tasks (e.g., backward counting, word generation) Participate in an 8-week training program, with sessions held twice a week lasting approximately 45-60 minutes Undergo assessments of gait, balance, and cognitive function before and after the intervention This study does not involve invasive procedures or biological sample collection. The findings are expected to contribute to the development of more effective dual-task rehabilitation strategies for individuals with multiple sclerosis.

Participants needed: 40
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Kutahya Health Sciences UniversityUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

Diagnosis of Multiple Sclerosis according to the revised McDonald criteria [+6]

MS relapse within the last 30 days [+4]

Status: Not yet recruiting

Mobile Health Application for Family Caregivers in Home Palliative Care

Family caregivers play a central role in providing daily care for patients receiving home palliative care. However, caregiving responsibilities may lead to increased burden, stress, and difficulties in symptom management and care coordination. Mobile health (mHealth) interventions may provide accessible education, symptom monitoring, and decision-support resources to improve caregiver outcomes and patient care. The aim of this randomized controlled trial is to evaluate the effectiveness of a mobile health application developed for family caregivers of patients receiving home palliative care. The primary outcome is caregiver competence. Secondary outcomes include caregiver burden, self-efficacy, patient symptom burden, emergency department visits, and hospitalizations. A total of 120 family caregivers will be randomly assigned to either the intervention group, which will use the mobile health application for 6 weeks in addition to usual care, or the control group, which will receive usual care alone. Outcomes will be assessed at baseline, post-intervention (Week 6), and follow-up (Week 18).

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Kutahya Health Sciences UniversityUpdated: Jun 26, 2026Locations: 1
Eligibility criteria

Family caregiver of a patient receiving home palliative care services. [+5]

Professional or paid caregivers. [+4]

Status: Not yet recruiting

Nurse-Led Telehealth Frailty Management in Older Adults

Frailty is an important geriatric syndrome associated with reduced physiological reserve, functional decline, falls, hospitalization, and increased health care use among older adults. This randomized controlled trial aims to evaluate the effect of a nurse-led telehealth-supported multicomponent frailty management program on frailty level and functional status in older adults living at home. The study will be conducted as a single-center, two-arm, parallel-group randomized controlled trial. A total of 100 older adults aged 65 years and older who are living at home and are frail or at risk of frailty will be randomly assigned to either the intervention group or the control group in a 1:1 ratio. Participants in the intervention group will receive an 6-week nurse-led telehealth-supported frailty management program, including weekly telephone counseling and individualized follow-up. Participants in the control group will continue usual care. Data will be collected at baseline, at 6 weeks, and at 18 weeks. The primary outcome is frailty level measured using the FRAIL Scale. Secondary outcomes include functional status, depressive symptoms, number of falls, emergency department visits, and hospitalizations.

Participants needed: 100
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Kutahya Health Sciences UniversityUpdated: Jun 16, 2026Locations: 1
Eligibility criteria

Aged 65 years or older [+5]

Having advanced cognitive impairment such as dementia [+5]

Status: Recruiting

Early Prediction of ICU Hypotension Using Machine Learning

This prospective observational study aims to develop and internally validate a machine learning model for the early prediction of hypotension in adult intensive care unit patients. The model will use routinely collected non-invasive vital signs, heart rate, medication-dose records, and fluid-balance data recorded during standard ICU care. No intervention will be assigned by the study, and patient management will not be changed according to the model output. The primary aim is to predict hypotension 30 minutes before its occurrence; shorter 5- and 15-minute prediction horizons will also be evaluated.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Kutahya Health Sciences UniversityUpdated: Jun 8, 2026Locations: 1
Eligibility criteria

Age 18 years or older [+5]

Age younger than 18 years [+4]

Status: Not yet recruiting

Nurse-Led Caregiver Support Program in Home Palliative Care

This randomized controlled trial aims to evaluate the effect of a nurse-led caregiver support program on caregiver competency and healthcare utilization among family caregivers of patients receiving home palliative care. Family caregivers in the intervention group will receive a structured 6-week nurse-led support program including face-to-face education, weekly telephone coaching, caregiver guidance materials, and decision support for symptom management and healthcare utilization. The control group will continue to receive routine home palliative care services. Primary outcome is caregiver competency. Secondary outcomes include caregiver burden, self-efficacy, patient symptom burden, emergency department visits, and hospitalizations.

Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Kutahya Health Sciences UniversityUpdated: Jun 8, 2026Locations: 1
Eligibility criteria

Adult family caregivers of patients receiving home palliative care services [+4]

Professional or paid caregivers [+2]

Status: Recruiting

ESPB vs SPSIP for Postoperative Analgesia After CABG

This prospective, randomized, active-controlled, double-blind, parallel-group study compares the postoperative analgesic efficacy and safety of ultrasound-guided bilateral Erector Spinae Plane Block (ESPB) versus bilateral Serratus Posterior Superior Intercostal Plane Block (SPSIPB) in adult patients (45-85 years, ASA I-III) undergoing elective coronary artery bypass graft surgery. The primary outcome is postoperative pain intensity assessed by Numeric Rating Scale (NRS) at 2, 4, 8, 16, 24, and 48 hours after surgery. Secondary outcomes include intraoperative fentanyl/remifentanil consumption, postoperative morphine consumption, patient-controlled analgesia (PCA) demand/delivery parameters (if PCA is used), need for rescue analgesics, extubation and mobilization times, peak inspiratory flow measured by incentive spirometry at predefined time points, ICU and hospital length of stay, recovery quality (QoR-15 at 0, 24, and 48 hours), mortality, and block-related adverse events.

Participants needed: 64
Trial details
Age: 45-85Biological sex: AllType: InterventionalSponsor: Kutahya Health Sciences UniversityUpdated: May 13, 2026Locations: 1
Eligibility criteria

Age 45-85 years [+3]

Emergency cases [+6]

Status: Recruiting

Effects of Hemiplegic Shoulder Pain on Upper Extremity Motor Function, Trunk Control, Fear of Falling, Mobility and Indepence in Activities of Daily Living in Patients With Stroke

This study aimed to examine the effects of hemiplegic shoulder pain on upper extremity motor assessment, trunk control, fear of falling, mobility, and functional indepedence patients with stroke.

Participants needed: 62
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Kutahya Health Sciences UniversityUpdated: Apr 30, 2026Locations: 1Duration: 1 Day
Eligibility criteria

Having a diagnosis of stroke [+3]

Having another neurological disease (except for stroke [+2]

Status: Recruiting

Predictors of Functional Status in Chronic Neck Pain

Although it has been reported that these problems seen together with neck pain are related to functional limitations and disability, there is still insufficient evidence regarding the relationship between factors affecting functional status and chronic neck pain symptoms in individuals with chronic neck pain. Furthermore, a mixed methodology approach has not been used to comprehensively investigate this relationship. Identifying factors affecting functional status in CNP will help guide the prevention, treatment, and management of neck pain. Therefore, the aim of this study is to investigate the relationships between functional status and psychosocial and bodily functions in CNP.

Participants needed: 80
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Kutahya Health Sciences UniversityUpdated: Apr 27, 2026Locations: 1
Eligibility criteria

patients aged 18-65 [+1]

patients with serious and secondary musculoskeletal diseases (inflammatory, neur... [+5]

Status: Not yet recruiting

The Effect of Body Percussion Training on Neuromotor Performance, Attention, and Functionality in Adolescents With Mild Intellectual Disability

The aim of this randomized controlled trial is to investigate the effects of group-based rhythm-based body percussion training on neuromotor performance, attention, and functionality in adolescents with mild intellectual disability. The study will be conducted in individuals aged 14-18 years with mild intellectual disability using a two-arm, parallel-group, evaluator-blind design. Participants will be assigned to experimental and control groups using a simple randomization method. The experimental group will receive structured body percussion training twice a week for 45 minutes over 8 weeks. This training consists of rhythmic patterns including clapping, knee tapping, chest tapping, finger snapping, and foot tapping, and will be presented as a progressively advancing program with metronome accompaniment. The control group will receive passive music listening without intervention for the same duration and frequency. Participants will be evaluated at two time points: before and after the intervention. Evaluation tools include: The tests cover neuromotor performance with the Minnesota Hand Skills Test and the Four Square Step Test, rhythm coordination with the Metronome Synchronization Test, attention with the Stroop Test, and functionality with the World Health Organization Disability Assessment Chart 2.0.

Participants needed: 25
Trial details
Age: 14-19Biological sex: AllType: InterventionalSponsor: Kutahya Health Sciences UniversityUpdated: Apr 28, 2026
Eligibility criteria

Being an adolescent aged 14-19 attending high school (e.g., special education hi... [+4]

Painful musculoskeletal/orthopedic (rheumatic, etc.) problems that may prevent p... [+8]

Status: Recruiting

Effect of Motor Imagery Training on Pain, Functionality, Proprioception and Kinesiophobia in Partial Rotator Cuff Tear

The aim of this study is to investigate the effects of motor imagery training on pain, functionality, proprioception and kinesiophobia in patients with partial rotator cuff tears. Participants will be randomly assigned to traditional physiotherapy and motor imagery groups. Interventions will be performed with a physiotherapist for a total of 20 sessions for 4 weeks, 5 days a week. The intervention program will be determined by the Specialist Physical Therapy Physician. Data will be collected before the study, at the end of the training in the 4th week and at the 8th week (follow-up evaluation). Motor imagery ability will be assessed with the Movement Imagery Questionnaire (MIQ-R), pain will be assessed with the Numerical Assessment Scale for functionality with the DASH, proprioception will be assessed with the inclinometer and kinesiophobia will be assessed with the Tampa Kinesiophobia Scale.

Participants needed: 80
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Kutahya Health Sciences UniversityUpdated: Apr 23, 2026Locations: 1
Eligibility criteria

Partial rotator cuff tear diagnosis. [+5]

Complete rotator cuff tear or conditions requiring surgical intervention, [+2]

Status: Not yet recruiting

Validity and Reliability of the Turkish Version of the 'Breathing Vigilance Questionnaire'

In the literature, assessment questionnaires related to dyspnea measure beliefs about breathing-related symptoms but do not directly measure breath awareness. For this purpose, the Breath Vigilance Questionnaire (BVQ) is a subjective questionnaire developed from the Pain Awareness Questionnaire that directly measures breath-specific awareness and includes questions evaluating the interaction between conscious monitoring and control of breathing and anxiety. The questionnaire, consisting of 6 questions, was developed on healthy individuals and its validity and reliability were established. It uses a 5-point Likert scale from 1 (never) to 5 (always), with scores ranging from 6 to 30, and higher scores indicate higher breath awareness . The reliability and validity of the Turkish version of the Breath Vigilance Questionnaire will assist researchers in assessing dysfunctional breathing and developing treatment strategies by evaluating breath awareness. Therefore, the study aimed to investigate the validity and reliability of the Turkish version.

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Kutahya Health Sciences UniversityUpdated: Apr 22, 2026Locations: 1Duration: 1 Day
Eligibility criteria

individuals without a self-reported diagnosis of respiratory and/or cardiac prob... [+2]

Individuals with symptomatic heart disease, a history of lung surgery, neurologi...

Status: Recruiting

HbA1c Levels and Gastric Emptying Assessed by Gastric Ultrasound

Delayed gastric emptying increases the risk of pulmonary aspiration during general anesthesia. Diabetes mellitus and poor long-term glycemic control have been associated with impaired gastric motility. Hemoglobin A1c (HbA1c) is a marker of long-term glycemic control; however, its relationship with gastric emptying in surgical patients is not fully understood. This prospective observational study aims to evaluate the association between HbA1c levels and gastric emptying using preoperative bedside gastric ultrasonography. Adult patients scheduled for elective surgery under general anesthesia will undergo gastric ultrasound examination after standard fasting. Gastric antral cross-sectional area and estimated gastric volume will be assessed and compared according to HbA1c levels. The findings of this study may help improve preoperative risk stratification for aspiration and support individualized anesthetic management in patients with impaired glycemic control.

Participants needed: 134
Trial details
Age: 18-70Biological sex: AllType: ObservationalSponsor: Kutahya Health Sciences UniversityUpdated: Apr 8, 2026Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

Effects of Aerobic Exercise in Rheumatoid Arthritis

This study aims to evaluate the effects of aerobic exercise therapy on quality of life, functional capacity, mood, and fatigue in patients with rheumatoid arthritis. Additionally, the study investigates the impact of aerobic exercise on inflammatory markers, pain, and disease activity.

Participants needed: 64
Trial details
Age: 30-70Biological sex: AllType: InterventionalSponsor: Kutahya Health Sciences UniversityUpdated: Apr 1, 2026Locations: 1
Eligibility criteria

Diagnosed with RA according to ACR/EULAR 2010 criteria [+3]

Cardiovascular diseases (CAD, heart failure, etc.) [+7]

Status: Not yet recruiting

High-Intensity Laser Therapy in Hemiplegic Shoulder Pain

This randomized, sham-controlled clinical trial aims to evaluate the effectiveness of high-intensity laser therapy (HILT) combined with exercise on pain, functional status, disability, and ultrasonographic findings in patients with hemiplegic shoulder pain following stroke.

Participants needed: 60
Trial details
Age: 30-75Biological sex: AllType: InterventionalSponsor: Kutahya Health Sciences UniversityUpdated: Mar 30, 2026Locations: 1
Eligibility criteria

Age 30-75 years [+4]

Neurological disorders (MS, Parkinson, etc.) [+6]

Status: Recruiting

Executive Function in Obese

This study was planned to examine the effect of executive function problems on physical performance and general well-being in obese individuals.

Participants needed: 100
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Kutahya Health Sciences UniversityUpdated: Mar 10, 2026Locations: 1
Eligibility criteria

Individuals volunteering for the study with BMI ≥30 kg/m2 [+5]

Being at a mental level that cannot understand and answer the questions posed [+5]

Status: Recruiting

Investigation of Motor Imagery Ability, Body Awareness and Cognitive Functions in Type 2 Diabetes Mellitus

The aim of this study is to examine the relationship between motor imagery skills, body awareness and cognitive functions in individuals with Type 2 Diabetes mellitus.

Participants needed: 100
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Kutahya Health Sciences UniversityUpdated: Mar 10, 2026Locations: 1
Eligibility criteria

Being a type 2 DM patient between the ages of 18-65 for at least 5 years, [+2]

Having previous experience with Motor Imagery techniques or training, [+3]

Status: Not yet recruiting

CBCT and Audiological Analysis of the TMJ-Tinnitus Relationship

The aim of this study is to investigate the relationship between Temporomandibular Disorders (TMD) and subjective tinnitus at both morphological and functional levels. Current literature suggests that somatosensory inputs from the temporomandibular joint (TMJ) and masticatory muscles can modulate auditory pathways, a phenomenon known as Somatosensory Tinnitus. However, the specific role of TMJ bone morphology and critical neighboring structures, such as the Petrotympanic Fissure (PTF), in this interaction remains unclear. In this clinical study, patients with tinnitus will undergo a comprehensive evaluation including Cone Beam Computed Tomography (CBCT) to quantitatively analyze condylar morphology and osteoarthritic changes. Additionally, audiological tests will be performed to assess the functional state of the auditory system. This multidisciplinary approach aims to clarify the biological link between TMD and tinnitus, potentially improving diagnostic protocols and highlighting the importance of TMJ stabilization in tinnitus management.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Kutahya Health Sciences UniversityUpdated: Mar 10, 2026Locations: 1
Eligibility criteria

Patients aged 18 years and older. [+4]

Presence of objective tinnitus (e.g., vascular or muscular origin). [+6]

Status: Not yet recruiting

Morphometric and Morphological Analysis of Cervical Vertebrae in Disc Displacement

Temporomandibular disorders (TMDs) are multifactorial clinical conditions affecting the masticatory muscles, the temporomandibular joint (TMJ), and the surrounding structures. The most common subtype is disc displacement, which is characterized by an abnormal position of the articular disc. Magnetic resonance imaging (MRI) is considered the gold standard for the diagnosis of disc displacement because it provides excellent soft tissue contrast, allows direct visualization of the disc, and enables dynamic evaluation. The parallel nature of mandibular and head-neck movements reflects the functional relationship between the temporomandibular and cervical neuromuscular systems. In addition, various craniofacial skeletal anomalies have been reported to be associated with disorders of the cervical vertebrae. TMD restricts mandibular movements and causes pain in the surrounding muscles, which may lead to referred pain in the neck, shoulder, and cervical muscles, thereby affecting head posture. Head and neck postural abnormalities are closely associated with cervical pain and dysfunction related to TMD. This relationship is thought to be bidirectional and can be explained through biomechanical, neurological, and pathophysiological mechanisms. In particular, upper cervical vertebral dysfunctions and changes in head position may influence the severity of TMD symptoms. For this purpose, lateral cephalometric radiography is frequently used to evaluate the hyoid position and the cervical spine in relation to the TMJ. Upper cervical vertebral anomalies and craniofacial morphological characteristics can be analyzed using these images.

Participants needed: 115
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Kutahya Health Sciences UniversityUpdated: Feb 24, 2026Duration: 1 Week
Eligibility criteria

Presence of TMJ symptoms on at least one side, including pain, abnormal mandibul... [+2]

Presence of malformations affecting the craniofacial region. [+7]

Status: Recruiting

Mobbing Exposure and Job Satisfaction Among Physiotherapists

Physiotherapists, who hold a significant place in the healthcare sector, are at risk for mobbing and low levels of job satisfaction due to both demanding physical working conditions and emotional stress. This study was designed to investigate the mobbing exposure and job satisfaction levels of physiotherapists.

Participants needed: 200
Trial details
Biological sex: AllType: ObservationalSponsor: Kutahya Health Sciences UniversityUpdated: Feb 11, 2026Locations: 1
Eligibility criteria

Currently working or having previously worked as a physiotherapist in Turkey. [+2]

Forms with incorrect answers to dummy questions (trap questions). [+1]

Status: Recruiting

Clay Therapy in Schizophrenia Patients

In recent years, art therapies have been discussed for their positive effects on mental disorders. One such therapy, clay therapy, is being studied to examine its effect on the functional recovery and individual and social performance of schizophrenia patients undergoing pharmacological treatment.

Participants needed: 17
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Kutahya Health Sciences UniversityUpdated: Jan 30, 2026Locations: 1
Eligibility criteria

Having been diagnosed with schizophrenia, [+8]

Being under 18 years of age, [+6]

Status: Recruiting

Effects of Swaddling and Nesting on Pain and Stress in Newborns

This study aims to investigate the effects of swaddling and cradling methods on pain and stress levels in newborn infants receiving respiratory support. Infants receiving respiratory support in the neonatal intensive care unit may experience stress and discomfort during treatment. In this study, two different care methods that help infants feel more comfortable and secure will be scientifically compared. Only one of the Swaddling or Nesting methods will be applied to the newborns participating in the study. These methods are comfort-enhancing care practices routinely used in neonatal intensive care that do not harm the baby. The newborn's heart rate, respiratory rate, oxygen level, pain and stress symptoms will be closely and safely monitored by the healthcare team. A pain-free saliva sample will be collected to assess the newborn's stress level. It does not involve needles, does not hurt, and takes approximately 2 minutes. Pain and stress levels will be assessed in a multifaceted manner using clinical observation, physiological parameters, and saliva cortisol levels. The study aims to contribute to the strengthening of evidence-based non-pharmacological care practices in neonatal intensive care.

Participants needed: 100
Trial details
Age: 0-28Biological sex: AllType: InterventionalSponsor: Kutahya Health Sciences UniversityUpdated: Jan 26, 2026Locations: 1
Eligibility criteria

Birth week greater than 35 weeks and birth weight greater than 2000 grams [+3]

Taking cortisol-containing medication during the antenatal period [+15]

Status: Not yet recruiting

Effects of Neurodynamic and Carpal Bone Mobilization in Mild-to-Moderate Carpal Tunnel Syndrome

Carpal tunnel syndrome (CTS) is the most common entrapment neuropathy caused by compression of the median nerve at the wrist. Conservative interventions such as splinting and manual therapy are frequently used in individuals with mild-to-moderate CTS. Neurodynamic mobilization and carpal bone mobilization aim to improve neural and soft tissue mobility; however, their comparative effects on clinical outcomes and median nerve morphology are not fully understood. This interventional, non-randomized clinical study aims to compare the clinical and ultrasonographic effects of neurodynamic mobilization plus splinting, carpal bone mobilization plus splinting, and splinting alone in patients with mild-to-moderate CTS. Ninety-three participants diagnosed with mild-to-moderate carpal tunnel syndrome based on electrodiagnostic criteria will be included. Participants will be allocated into three parallel groups without randomization. All participants will receive a neutral-position wrist splint as standard conservative care. Two intervention groups will additionally receive either neurodynamic mobilization exercises or carpal bone mobilization techniques administered by a physiotherapist for four weeks. Clinical outcomes and median nerve morphology will be evaluated at baseline and immediately after the intervention period. The primary outcome is the change in the Boston Carpal Tunnel Questionnaire score. Secondary outcomes include pain intensity, neuropathic pain, functional disability, muscle strength, pressure pain threshold, and ultrasonographic measurements of the median nerve.

Participants needed: 93
Trial details
Age: 20-55Biological sex: AllType: InterventionalSponsor: Kutahya Health Sciences UniversityUpdated: Jan 22, 2026Locations: 1
Eligibility criteria

Diagnosis of mild-to-moderate carpal tunnel syndrome confirmed by electrodiagnos... [+2]

Previous carpal tunnel surgery [+4]

Status: Recruiting

Test-Retest Reliability of Grip Force Sense for Proprioception Assessment

The aim of this study is to investigate the test-retest reliability of the grip force sense, a component of proprioception, using a dynamometer that is easily accessible and usable in a clinical setting. This provides an accessible assessment method for research in the field of proprioception.

Participants needed: 55
Trial details
Age: 18-24Biological sex: AllType: ObservationalSponsor: Kutahya Health Sciences UniversityUpdated: Jan 15, 2026Locations: 1
Eligibility criteria

Age 18-24 years [+1]

Having a history of hand surgery [+1]

Status: Recruiting

Investigation of the Effects of Early Skin-to-Skin Contact on Mother and Baby in Cesarean Births

The rate of cesarean birth continues to increase in the world and in our country. As with all surgeries, the risks of cesarean birth include the possibility of bleeding and infection, prolonged recovery time after birth, delays in initiating breastfeeding and skin-to-skin contact (SSC), and increased likelihood of complications in future pregnancies. While many hospitals apply SSC after normal births, it is known that the number of hospitals that apply SSC in the operating room after cesarean birth is very few. Factors that prevent the initiation of SSC after cesarean birth include the effect of the current operating room culture, the physiological evaluation process of the baby after birth, the presence of procedures such as measuring body weight, aspiration, and Apgar score evaluation. Since the mother and baby are separated after cesarean birth, the mother's initiation of breastfeeding in the first hour of life may be delayed, and the duration of exclusive breastfeeding may be shortened. The 90-minute uninterrupted skin-to-skin contact during which the baby is dried and placed directly on the mother's bare chest after birth maximizes the chance that babies are physically ready to breastfeed. Although there are studies showing the benefits of SSC application in the operating room such as breastfeeding rates, maintaining the body temperature of the newborn, reducing maternal stress levels, and increasing oxytocin levels, a limited number of studies have been reached in the literature using SSC application guidelines developed to ensure the sustainability of SSC application in the operating room, post-op care unit, and obstetrics clinic. The first contribution of this planned study to the literature will be to standardize SSC application with SSC checklists prepared for use in the cesarean operation room, post-op care unit, and obstetrics ward based on SSC application guidelines. As a second contribution, considering the conditions of the health institution where the study will be conducted, the effects of starting SSC as early as possible and applying it in the cesarean operation room, post-op care unit, and obstetrics ward on the stress level of newborns, sucking success, and pain and salivary cortisol (stress) levels of mothers will be evaluated.

Participants needed: 120
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Kutahya Health Sciences UniversityUpdated: Jan 14, 2026Locations: 1
Eligibility criteria

Planning a cesarean section with spinal anesthesia [+12]

Caesarean births performed with general anesthesia [+1]

Status: Recruiting

Drug-Coated Coronary Balloons in Different Clinical Scenarios

Coronary stents are the best treatment method ever accepted in the treatment of coronary artery stenoses. Due to some limitations and complications of stent use, the operators tried to find new solutions. Drug Coated Balloons (DCBs) have been accepted as a new method in the treatment of in-stent restenosis and small vessel disease. Furthermore, they have been used in the treatment of de novo coronary lesions, chronic total occlusions and bifucation lesions. But data is limited in the short and long term success of DCBs in all these clinical scenarios. In our study we aimed to investigate the procedural success and short and long term outcomes of DCB use in different clinical scenarios.

Participants needed: 1,500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Kutahya Health Sciences UniversityUpdated: Jan 13, 2026Locations: 5Duration: 1 Year
Eligibility criteria

Not listed