Clinical trials

51

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Condition / disease
Location
Status: Recruiting

The Effect of Comorbid Alcohol/Substance Use

Study Design This study was designed as a comparative, cross-sectional case-control study examining the effect of comorbid alcohol and substance use disorder (ASUD) on clinical course and social inclusion among individuals with severe mental illness followed at a Community Mental Health Center (CMHC). The study did not involve any interventions. Aim The aim of this study is to examine the effect of comorbid alcohol and substance use on clinical course parameters-such as number of hospitalizations and medication dosages-and on social inclusion indicators-such as employment, social participation, and social adjustment-among individuals with severe mental illness followed at the CMHC, in comparison with a matched control group without substance use. Research Questions What are the rates of comorbid alcohol and substance use among patients with severe mental illness followed at the CMHC? What are the current addiction symptoms, number of hospitalizations, and employment rates among individuals with severe mental illness and comorbid ASUD? What is the level of continuity of CMHC engagement and social participation among individuals with severe mental illness and comorbid ASUD, and what factors influence it? How does the level of social inclusion among individuals with severe mental illness and comorbid ASUD compare with that of individuals without ASUD? Hypotheses H1: The average annual number of hospitalizations among individuals with a dual diagnosis (severe mental illness + ASUD) followed at the CMHC is significantly higher than among those without substance use. H2: Among individuals with a dual diagnosis, the daily medication doses (e.g., chlorpromazine equivalents) required to control psychotic or manic symptoms are higher than in the control group. H3: Social inclusion is lower among patients with substance use compared with the control group. H4: Employment rates among individuals with a dual diagnosis are significantly lower than among those with severe mental illness alone. H5: Substance use negatively affects patients' social participation, including involvement in activities and friendships. H6: Attendance rates at CMHC workshops and rehabilitation programs are lower among individuals with substance use compared with the control group.

Participants needed: 297
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Abant Izzet Baysal UniversityUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

Being 18 years of age or older, [+2]

Individuals diagnosed with organic brain damage or neurodevelopmental disorders... [+1]

Status: Recruiting

Bladder and Bowel Functions, Participation and Quality of Life in Children With Intellectual Disabilities

Many neurodevelopmental, psychiatric, and medical disorders are commonly associated with intellectual disability. The presence of neurodevelopmental and psychiatric (NDP) comorbidities has been reported to negatively impact the clinical outcomes of bowel or bladder dysfunction. Pediatric bladder and bowel dysfunction (BBD) is a common but underdiagnosed condition characterized by a spectrum of lower urinary tract symptoms and is often associated with constipation. Lower urinary tract symptoms include dysuria, urinary urgency, daytime incontinence, and enuresis, while bowel symptoms include constipation and encopresis. Most BBD cases are functional and not neurogenic in origin. In children with special needs, all types of urinary incontinence are reported to occur more frequently compared to children without developmental or behavioral disabilities. Intellectual disability (IQ \<70) is also identified as a significant risk factor for urinary incontinence, with prevalence increasing as IQ decreases. In these children, lower urinary tract symptoms such as overactive bladder, dysfunctional voiding, and low fluid intake are also observed. Furthermore, according to support plans and medical records, 94% of individuals with intellectual and multiple disabilities experience constipation. Interestingly, lower levels of intellectual disability (profound and severe ID) have been associated with a lower prevalence of constipation. Although there are studies in the literature examining bladder and bowel functions separately in specific diagnostic groups with intellectual disability, the number of studies that assess bladder and bowel functions together in children with any form of intellectual disability is limited. Moreover, to our knowledge, there is no study in the literature that evaluates bladder and bowel functions along with child participation and parental quality of life in children with intellectual disability. Based on this gap in the literature, the aim of our study is to examine bladder and bowel functions, participation, and quality of life in children with intellectual disability

Participants needed: 100
Trial details
Age: 5-12Biological sex: AllType: ObservationalSponsor: Abant Izzet Baysal UniversityUpdated: Jun 17, 2026Locations: 1
Eligibility criteria

Aged between 5 and 12 years [+4]

Having a diagnosis of physical disability [+9]

Status: Not yet recruiting

The Effect of the Model-Based Care Decision Support System in Pediatric Intensive Care on Nurses' Decision Making and Opinions

The Effect of the Model-Based Care Decision Support System in Pediatric Intensive Care on Nurses' Decision Making and Opinions

Participants needed: 35
Trial details
Age: Up to 18Biological sex: AllType: InterventionalSponsor: Abant Izzet Baysal UniversityUpdated: May 22, 2026Locations: 1
Eligibility criteria

Nurses with at least 6 months of experience in intensive care [+2]

Nurses who are temporarily on leave due to reasons such as maternity leave or un...

Status: Not yet recruiting

The Effect of Self-Acupressure on Blood Pressure, Stress, and Well-Being Levels in Individuals With Hypertension

This randomized controlled trial examines the effects of nurse-led self-acupressure at HT7, LI4, PC6, and EX3 points on blood pressure, stress, and well-being in adults with primary hypertension. Participants are randomized to real acupressure, sham acupressure, or usual care groups for 2 weeks.

Participants needed: 72
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Abant Izzet Baysal UniversityUpdated: May 14, 2026Locations: 1
Eligibility criteria

Aged 18-65 years [+5]

Secondary hypertension [+7]

Status: Recruiting

Turkish Adaptation of the CSQ-VR

The Cybersickness in Virtual Reality Questionnaire (CSQ-VR) is a tool designed to measure the presence and intensity of cybersickness symptoms experienced in VR. The CSQ-VR is an adapted and improved version of the Cybersickness section of the Virtual Reality Neuroscience Questionnaire (VRNQ). The aim of this study is to examine the validity and reliability of the Turkish version of the CSQ-VR.

Participants needed: 42
Trial details
Age: 18-30Biological sex: AllType: ObservationalSponsor: Abant Izzet Baysal UniversityUpdated: May 11, 2026Locations: 1Duration: 1 Day
Eligibility criteria

Voluntary agreement to participate in the study [+1]

Presence of amblyopia, strabismus, or pathologies impairing focus, depth percept... [+1]

Status: Recruiting

Patient-Specific 3D Action Observation Training in Parkinson's Disease

Although studies exist demonstrating the effects of single-session action observation training on bradykinesia in patients with Parkinson's disease, research investigating the long-term application of such training remains limited. Furthermore, the broader literature indicates that action observation training has typically been conducted in simulated environments or by using recordings obtained from healthy individuals. The aim of the present study is to examine the effects of action observation training, delivered in a fully immersive virtual reality environment using each patient's own 3D motion recordings, on bradykinesia and other disease-related parameters.

Participants needed: 24
Trial details
Age: 50-85Biological sex: AllType: InterventionalSponsor: Abant Izzet Baysal UniversityUpdated: May 11, 2026Locations: 1
Eligibility criteria

Voluntary agreement to participate in the study [+4]

Presence of additional neurological disorders other than Parkinson's disease [+4]

Status: Recruiting

Association Between Periodontal Status and the Prevalence of Entamoeba Gingivalis and Trichomonas Tenax

This prospective observational study aims to investigate the prevalence and clinical significance of two oral protozoa, Entamoeba gingivalis and Trichomonas tenax, among patients attending the Bolu Abant İzzet Baysal University Faculty of Dentistry, Department of Periodontology. While the oral microbiome typically maintains a delicate balance, disruptions in this ecosystem are thought to trigger periodontal diseases. Recent evidence suggests that these parasites may contribute to increased inflammation and tissue destruction, potentially playing a role in the etiology of gingivitis and periodontitis. The study will include 120 participants aged 18 and older who meet the inclusion criteria. Following the collection of demographic data and oral hygiene habits via a questionnaire, a single calibrated examiner will perform comprehensive clinical periodontal examinations. Measurements will include plaque index (PI), gingival index (GI), bleeding on probing (BOP), probing pocket depth (PPD), clinical attachment loss (CAL), and gingival recession (GR) based on the 2017 World Workshop Classification of Periodontal and Peri-Implant Diseases and Conditions. To detect the presence of parasites, unstimulated whole saliva samples and subgingival plaque samples from the deepest periodontal pockets will be collected from each participant. These samples will be analyzed immediately at the Parasitology Laboratory using light microscopy (10X and 40X magnification) to identify live trophozoites. By evaluating the relationship between parasite prevalence and periodontal status, this research aims to contribute to the limited literature on oral protozoa in Turkey and increase clinical awareness regarding their impact on oral health.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Abant Izzet Baysal UniversityUpdated: May 8, 2026Locations: 1Duration: 1 Day
Eligibility criteria

Participants aged 18 years or older. [+3]

Use of systemic antibiotics within the last 3 months. [+4]

Status: Recruiting

Virtual Reality Based Mirror Therapy

The aim of this study is to examine the effectiveness of 3D virtual reality assisted mirror therapy based rehabilitation applications compared to classical methods used in stroke rehabilitation.

Participants needed: 56
Trial details
Age: 40-80Biological sex: AllType: InterventionalSponsor: Abant Izzet Baysal UniversityUpdated: May 7, 2026Locations: 1
Eligibility criteria

Have a ischemic stroke [+6]

Additional neurologic diseases [+7]

Status: Recruiting

ORAL HYGIENE, PERIODONTAL STATUS AND QUALITY OF LIFE

This cross-sectional study aims to evaluate the relationship between oral hygiene habits, periodontal status, and oral health-related quality of life in adult individuals. A total of approximately 160 participants attending the Department of Periodontology will be included. Periodontal status will be assessed using standard clinical parameters, including probing depth, clinical attachment loss, bleeding on probing, and plaque index. In addition, the Periodontal Inflamed Surface Area (PISA) will be calculated to quantify inflammatory burden. Oral health-related quality of life will be evaluated using the OSHIP-Perio questionnaire, a validated patient-reported outcome measure specific to periodontal conditions. The study will investigate the association between clinical periodontal findings, oral hygiene practices, and quality of life outcomes. The findings are expected to provide a comprehensive understanding of both clinical and patient-centered aspects of periodontal disease and contribute to improved individualized treatment approaches.

Participants needed: 160
Trial details
Biological sex: AllType: ObservationalSponsor: Abant Izzet Baysal UniversityUpdated: Apr 30, 2026Locations: 1
Eligibility criteria

Individuals aged 18 years and older [+1]

Use of antibiotics or anti-inflammatory drugs within the last 3 months [+3]

Status: Not yet recruiting

The Effect of Pink Noise and the Quiet Night Intervention on Sleep Parameters in Intensive Care Unit Patients: A Single-Center Randomized Controlled Trial

Sleep disruption is common in adult intensive care unit (ICU) patients and is often worsened by environmental noise and nighttime care activities. Poor sleep may negatively affect recovery and well-being. This single-center, three-arm randomized controlled trial will evaluate the short-term effects of two non-pharmacological interventions-(1) pink-brown noise masking and (2) a quiet time intervention-on objective sleep parameters in adult ICU patients, compared with standard care. Sleep outcomes will be measured using actigraphy-based wearable monitoring, including total sleep time, sleep efficiency, sleep onset latency, wake after sleep onset, and number of awakenings. Results are expected to support evidence-based nursing approaches to improve sleep in ICU patients.

Participants needed: 18
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Abant Izzet Baysal UniversityUpdated: Apr 22, 2026Locations: 1
Eligibility criteria

Adults aged 18 years and older [+4]

Severe hearing impairment preventing use of acoustic interventions [+4]

Status: Recruiting

The Effect of Emotional Freedom Technique on Parents' Anxiety Level: Newborn Hearing Screening

Newborn hearing screening (NHS) is a standard procedure that often triggers acute anxiety in parents. While Emotional Freedom Technique (EFT) has demonstrated efficacy in reducing psychological distress across various clinical settings, its specific application to parental anxiety during the neonatal screening period remains under-researched. This study addresses this gap by investigating the impact of a targeted EFT intervention on anxiety levels in mothers awaiting their newborns' first hearing tests. The primary objective is to determine if a brief, 15-minute EFT session reduces maternal anxiety more effectively than a standard waiting period. Participants are randomly assigned to either an intervention group, where they perform a structured acupoint tapping sequence, or a control group that receives no active intervention. Anxiety is assessed using validated scales immediately before and after the 15-minute period to capture acute changes in distress. The researchers hypothesize that applying EFT regarding the procedure will significantly reduce parental anxiety levels compared to the non-intervention group.

Participants needed: 70
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Abant Izzet Baysal UniversityUpdated: Apr 15, 2026Locations: 2
Eligibility criteria

Parents of neonates who are undergoing the newborn hearing screening (NHS) for t... [+3]

Known history of diagnosed psychiatric disorders or epilepsy. [+3]

Status: Recruiting

Gas6 and Soluble MerTK in Periodontal Diseases

This study aimed to investigate gingival crevicular fluid (GCF) and serum soluble MerTK (sMerTK) and Gas6 levels in periodontal health and disease. A total of 90 individuals, 30 patients with stage III grade B periodontitis, 30 with gingivitis and 30 periodontally healthy individuals were included. Whole-mouth and site-specific clinical periodontal parameters including probing depth, clinical attachment level, bleeding on probing, gingival index, plaque index were recorded. GCF and serum sMerTK and Gas6 levels were measured by enzyme-linked immunosorbent assay. Statistical analysis was performed by using non-parametric tests.

Participants needed: 90
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Abant Izzet Baysal UniversityUpdated: Apr 16, 2026Locations: 1
Eligibility criteria

Individuals without systemic diseases that may affect periodontal tissues (such... [+5]

Pregnant or lactating individuals [+2]

Status: Not yet recruiting

The Effect of Proprioceptive Neuromuscular Facilitation on Haemodynamic Responses in a Neurological Intensive Care

Although there are studies examining the effect of actively performed PNF exercises on haemodynamic responses in intensive care patients and healthy individuals, there are no studies investigating their effect on circulation and haemodynamic responses in unconscious patients. Therefore, this study was designed to investigate the acute effects of proprioceptive neuromuscular facilitation (PNF) exercises on peripheral circulation and haemodynamic responses in patients admitted to a neurological intensive care unit. Hypotheses: H1-1: Passively administered PNF exercises have beneficial effects on peripheral circulation. H2-1: Passively administered PNF exercises have beneficial effects on haemodynamic responses.

Participants needed: 24
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Abant Izzet Baysal UniversityUpdated: Apr 13, 2026
Eligibility criteria

Patients being monitored in the neurology intensive care unit [+4]

Presence of haemodynamic instability [+4]

Status: Recruiting

Neuropathic Pain, Catastrophizing, and Adherence in SAIS

Subacromial impingement syndrome is one of the most common causes of shoulder pain and may negatively affect daily activities and quality of life. While shoulder pain is usually considered nociceptive, some patients may also have a neuropathic pain component, which can influence symptom severity and treatment outcomes. In addition, psychological factors such as pain catastrophizing and adherence-related behavior may play an important role in recovery. This prospective observational study aims to evaluate the presence of neuropathic pain in patients with subacromial impingement syndrome and to investigate its relationship with pain catastrophizing and adherence-related behavior. Patients undergoing a standard physical therapy program will be assessed at the beginning and after completion of treatment using validated clinical scales. The findings of this study may help to better understand the interaction between pain characteristics, psychological factors, and adherence-related behavior, and contribute to the development of more individualized rehabilitation strategies

Participants needed: 75
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Abant Izzet Baysal UniversityUpdated: Apr 8, 2026Locations: 1
Eligibility criteria

Unilateral subacromial impingement syndrome lasting at least 3 months [+2]

Upper extremity entrapment neuropathy or polyneuropathy [+10]

Status: Not yet recruiting

Tele-Nursing-Supported Mindfetalness: Anxiety and Prenatal Attachment

The goal of this clinical trial is to compare the effects of tele-nursing-supported Mindfetalness method versus Mindfetalness alone method on maternal anxiety and prenatal attachment in pregnant women. The main questions it aims to answer are: * H1: Tele-nursing-supported Mindfetalness method will significantly reduce state anxiety (STAI-S) levels in pregnant women over time compared to Mindfetalness alone method. * H2: Tele-nursing-supported Mindfetalness method will significantly reduce trait anxiety (STAI-T) levels in pregnant women over time compared to Mindfetalness alone method. * H3: Tele-nursing-supported Mindfetalness method will significantly increase prenatal attachment (PAI) levels in pregnant women over time compared to Mindfetalness alone method. Researches will compare tele-nursing-supported Mindfetalness to Mindfetalness alone to see if tele-nursing support significiantly reduces state and trait anxiety levels and significiantly increases prenatal attachment levels in pregnant women over time. Participants will; * Attend a single, face-to-face Mindfetalness training session at the beginning of the study to learn technique and application procedures correctly. * Practice Mindfetalness method daily for 15 minutes throughout the 8-week study period. * Complete a daily compliance tracking chart to record their adherence to the Mindfetalness method of their practice. * Complete the State-Trait Anxiety Inventory (STAI) and the Prenatal Attachment Inventory (PAI) at baseline and during 4th and 8th-week follow-up measurements to track changes over time.

Participants needed: 68
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Abant Izzet Baysal UniversityUpdated: Apr 7, 2026Locations: 1
Eligibility criteria

Aged 18 years or older [+6]

Having a high-risk pregnancy (e.g., preterm labor threat, preeclampsia, gestatio... [+5]

Status: Recruiting

Musculoskeletal Disorders of Postgraduate Dentistry Students and Specialist Dentists

This study aimed to assess the prevalence of MSDs and the level of ergonomics knowledge among dentists who are specializing in different branches or have completed specialist training.

Participants needed: 90
Trial details
Age: 25-60Biological sex: AllType: ObservationalSponsor: Abant Izzet Baysal UniversityUpdated: Apr 1, 2026Locations: 1
Eligibility criteria

Being between 25 and 60 years of age [+1]

Having physical conditions such as rheumatoid arthritis or fibromyalgia [+3]

Status: Recruiting

Investigation of the Effects of Complex Decongestive Physiotherapy on Sleep Quality and Quality of Life in Women With Breast Cancer Related Lymphedema

Breast cancer is the most common type of cancer among women globally and has the highest mortality rate. Surgical interventions are typically required in the treatment of breast cancer, but these procedures can lead to complications such as infection, seroma, hematoma, cellulitis, and particularly lymphedema due to disruptions in the physiology of axillary lymphatic vessels. Breast Cancer-Related Lymphedema (BCRL) commonly develops within the first two years following surgical intervention and its incidence varies depending on the surgical method used. The incidence of lymphedema after Sentinel Lymph Node Biopsy (SLNB) is around 5%, whereas it increases to 30-50% after Axillary Lymph Node Dissection (ALND). BCRL significantly impacts the quality of life (QoL) through physical symptoms such as swelling, pain, tightness, and limited range of motion, as well as psychosocial issues including depression, social isolation, and sleep disturbances. Sleep disorders, in particular, are associated with depression and contribute to a further decline in QoL. In the treatment of BCRL, both conservative (non-surgical) and surgical methods are traditionally employed. Complex Decongestive Physiotherapy (CDP) is considered the gold standard for the conservative management of lymphedema. CDP comprises a two-phase treatment process. The first phase, known as the "Decongestion Phase," generally lasts 2-4 weeks and includes manual lymphatic drainage (MLD), skin care, compression therapy with multi-layered short-stretch bandages, and muscle-pumping exercises. The second phase, the "Maintenance Phase," is more prolonged and aims to sustain the results achieved in Phase 1. It includes compression with low-stretch elastic garments, skin care, exercises, and patient-administered MLD as needed. The primary objectives of CDP are to improve lymphatic circulation, reduce swelling, pain, and tightness, increase the range of motion, and ultimately improve the QoL. Studies have shown that CDP significantly enhances sleep quality and QoL in women with BCRL. However, most existing studies examine all stages of BCRL without comparing the effects of CDP across different stages. The impact of CDP on sleep and QoL may vary depending on the stage of BCRL, highlighting the need for specific research on its effects in particular populations. Furthermore, many studies lack follow-up data, leaving the Maintenance Phase of CDP largely unexplored. This study aims to investigate the effects of CDP, including both the Decongestion and Maintenance phases, on sleep quality and QoL specifically in women with Stage II BCRL.

Participants needed: 31
Trial details
Age: 18-85Biological sex: FemaleType: InterventionalSponsor: Abant Izzet Baysal UniversityUpdated: Apr 1, 2026Locations: 2
Eligibility criteria

Participants must be aged between 18 or 85 years, [+3]

refusal to participate in the study [+6]

Status: Recruiting

Robot-Assisted Gait Training vs Visual Feedback Balance Training in Stroke

Stroke frequently leads to balance impairment and gait dysfunction, increasing fall risk and limiting functional independence. Technology-assisted rehabilitation approaches such as robot-assisted gait training and visual feedback balance training have been shown to improve balance and mobility in stroke patients. This randomized, assessor-blinded clinical trial aims to compare the effects of robot-assisted gait training and visual feedback balance training on balance and gait outcomes in patients with subacute and chronic stroke. Both interventions are part of routine clinical rehabilitation practice. Participants will be evaluated at baseline and after 4 weeks of intervention using clinical balance, gait, and functional assessments.

Participants needed: 60
Trial details
Age: 21-85Biological sex: AllType: InterventionalSponsor: Abant Izzet Baysal UniversityUpdated: Mar 18, 2026Locations: 1
Eligibility criteria

Age 21-85 years [+5]

Unstable cardiopulmonary conditions [+3]

Status: Recruiting

Effect of Dehydration on Sleep Quality, Cognitive Skills, and Electromyographic Responses in Combat Athletes

This study examines the effects of rapid dehydration-induced weight loss on combat athletes' sleep quality, cognitive skills, and isokinetic strength performance. The research documents both benefits and risks of weight-cutting practices for athletes, coaches, and medical staff in weight-class sports. Findings will guide safer weight management approaches and inform potential revisions to international weigh-in protocols, while contributing valuable insights to sports science.

Participants needed: 12
Trial details
Age: 17-28Biological sex: MaleType: InterventionalSponsor: Abant Izzet Baysal UniversityUpdated: Mar 16, 2026Locations: 1
Eligibility criteria

Voluntary participation [+3]

Using of sleep-related medications [+1]

Status: Not yet recruiting

Effectiveness of a Sleep Hygiene Education in Female Para Athletes

It is imperative to recognise elite female sitting volleyball players as a high-risk group with regard to sleep deprivation. However, there is a paucity of research investigating the efficacy of sleep hygiene education for this demographic. The objective of this study is to The present study aims to examine the effect of sleep hygiene education on sleep quality and behaviour in elite female sitting volleyball players using mixed methods.

Participants needed: 12
Trial details
Biological sex: FemaleType: InterventionalSponsor: Abant Izzet Baysal UniversityUpdated: Feb 27, 2026Locations: 1
Eligibility criteria

Being an elite athlete who is a member of the Turkey Women's National Sitting Vo... [+5]

Inability to participate regularly in training sessions during the study period... [+2]

Status: Not yet recruiting

Effects Of Spiral Strapping Systems On Upper Limb Function In Unilateral Spastic Cerebral Palsy

The purpose of this clinical study is to learn whether two different spiral strapping systems can improve arm and hand use in children with unilateral spastic cerebral palsy. These strapping systems are used to support the arm in a more functional position and to help children control their movements during daily activities. This study aims to answer the following main questions: Does spiral strapping help children use their arm and hand more effectively in daily activities? Does spiral strapping improve hand skills and grip strength? Is there a difference in effect between the two spiral strapping systems? To answer these questions, researchers will divide participants into three groups. One group will receive a standard rehabilitation program plus TheraTogs® spiral strapping. A second group will receive the same rehabilitation program plus TogRite™ spiral strapping. The third group will receive the rehabilitation program only. Participants will: Take part in rehabilitation sessions twice a week for eight weeks. Use spiral strapping during some sessions, depending on their group. Complete arm and hand assessments at the beginning and at the end of the study. The results of this study may help develop simple and practical rehabilitation approaches that support children with cerebral palsy in becoming more independent in daily life.

Participants needed: 27
Trial details
Age: 4-15Biological sex: AllType: InterventionalSponsor: Abant Izzet Baysal UniversityUpdated: Feb 18, 2026
Eligibility criteria

Not listed

Status: Not yet recruiting

Emotional Eating, Sleep Quality, Mental State and Metabolic Syndrome

In predominantly medication-naïve schizophrenic patients, those exhibiting partial metabolic disorders have significantly worse sleep quality and sleep onset time; poor sleep predicted metabolic dysregulation even after controlling for confounding factors. Mental health, sleep, and eating behavior interact in ways that strongly influence the risk of obesity and MetS. Emotional eating (eating in response to emotions rather than hunger) is central to this network and appears to be closely associated with psychiatric illnesses, particularly depression, anxiety, and sleep disorders. There is a continuing need to elucidate the frequency, level, and relationship of emotional eating with other factors in individuals with SMI. Therefore, this study aims to elucidate this complex relationship, thereby shedding light on new ways to reduce metabolic risks in psychiatric patients.

Participants needed: 78
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Abant Izzet Baysal UniversityUpdated: Feb 13, 2026
Eligibility criteria

Being registered with the Bolu İzzet Baysal Mental Health and Diseases Hospital... [+6]

Having a diagnosis of mental retardation, [+2]

Status: Recruiting

Short-Term Effects of Antihypertensive Drugs on Postural Balance and Fall Risk

The goal of this clinical trial is to compare the short-term effects of three commonly prescribed antihypertensive drug classes (beta-blockers, ACE inhibitors, and calcium channel blockers) on postural balance and fall risk in adults with newly diagnosed primary hypertension. The main questions it aims to answer are: * Do different antihypertensive drugs affect objective balance performance and fall risk? * What are the effects of these medications on dizziness and fear of falling? Researchers will use a balance analysis system (Biodex Balance System) and self-reported scales (Dizziness Handicap Inventory and Falls Efficacy Scale) to assess outcomes. Participants will: * Be randomly assigned to one of three drug groups (metoprolol, ramipril, or amlodipine) * Be evaluated at baseline (prior to treatment), at 2 weeks, and at 4 weeks after starting treatment * Complete balance tests and questionnaires at each time point This study aims to provide clinical insight into how commonly used blood pressure medications may impact balance and fall risk in real-world settings.

Participants needed: 186
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Abant Izzet Baysal UniversityUpdated: Feb 12, 2026Locations: 1
Eligibility criteria

Aged between 18 and 75 years [+5]

Secondary hypertension [+5]

Status: Recruiting

Multisensory and Cognitive Interventions in the ICU: Effects on Health and Recovery

The goal of this clinical trial is to examine the effects of sensory and cognitive stimulation on physiological, psychological, and functional recovery in adult patients after cardiac surgery who are treated in the intensive care unit (ICU). The main questions it aims to answer are: * Does sensory and/or cognitive stimulation reduce anxiety and improve hemodynamic stability in ICU patients? * Does it enhance physical function and independence during early rehabilitation in the ICU? Researchers will compare four groups: 1. Standard care (control), 2. Cognitive stimulation, 3. Auditory stimulation (music), 4. Multisensory stimulation (touch + smell) to assess which intervention is most effective in improving recovery parameters. Participants will: * Be randomly assigned to one of four groups during early mobilization in the ICU * Receive a 30-minute intervention session depending on group assignment * Be evaluated for heart rate, blood pressure, oxygen saturation, anxiety (VAS), physical function (PFIT, FIM), and satisfaction before and after the session

Participants needed: 125
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Abant Izzet Baysal UniversityUpdated: Feb 12, 2026Locations: 1
Eligibility criteria

Age between 18 and 80 years [+4]

Diagnosis of ICU delirium or altered mental status [+4]

Status: Recruiting

Virtual Reality Mirrors Therapy Usability

Mirror therapy has been shown to support motor recovery by stimulating neural mechanisms through visual feedback. Recent technological advancements, particularly in virtual reality (VR), have enabled the development of more immersive and interactive rehabilitation tools. This study focuses on evaluating the usability of a novel, Leap Motion-based Virtual Reality Mirror Therapy (VRMT) system designed to enhance upper limb rehabilitation in stroke patients by combining traditional mirror therapy principles with engaging, gamified digital environments.

Participants needed: 172
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Abant Izzet Baysal UniversityUpdated: Feb 5, 2026Locations: 2
Eligibility criteria

Stereo acuity score of 3552 arc/sec in the Titmus Fly Test [+1]

Severe sensory impairments (vision or hearing) [+1]