Clinical trials

20

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

Condition / disease
Location
Status: Not yet recruiting

Effects of Music Therapy in Chronic Neck Pain

This study aims to investigate the effects of music therapy on pain, cervical position sense, and balance in individuals with chronic neck pain. Chronic neck pain is a common musculoskeletal disorder that may impair proprioception and postural control, negatively affecting daily functioning and quality of life. Music therapy is a safe, low-cost, and non-pharmacological intervention with potential benefits for pain management and sensorimotor function; however, evidence regarding its effects in musculoskeletal rehabilitation is limited. In this study, nineteen individuals with chronic neck pain will listen to instrumental Turkish Classical Music in the Nihavend mode for 60 minutes. Pain intensity, cervical position sense, and static and dynamic balance will be assessed before and after the intervention. The findings are expected to provide evidence for the clinical use of music therapy as an adjunctive treatment in chronic neck pain rehabilitation.

Participants needed: 19
Trial details
Age: 20-50Biological sex: AllType: InterventionalSponsor: Karabuk UniversityUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

Being between 20-50 years old [+3]

Patients with surgical indications for and/or who have undergone surgery in the... [+5]

Status: Not yet recruiting

Symptom Severity, Posture, Pain, and Physical Activity in Gastroesophageal Reflux Disease

This study is a cross-sectional research designed to investigate symptom severity, posture, musculoskeletal pain, and physical activity levels in individuals with gastroesophageal reflux disease (GERD).

Participants needed: 51
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Karabuk UniversityUpdated: Jun 15, 2026
Eligibility criteria

Being diagnosed with gastroesophageal reflux disease (GERD) [+2]

Presence of a diagnosed psychiatric disorder [+1]

Status: Not yet recruiting

The Effect of Foot Reflexology in Women With Migraine

This prospective randomized controlled study aims to investigate the effects of foot massage on pain, anxiety, kinesiophobia, and postural control in women aged 18-45 years diagnosed with migraine who attend the Neurology Outpatient Clinic of Karabük University Karabük Training and Research Hospital. Participants who meet the inclusion and exclusion criteria will be randomly allocated into either a foot massage group or a control group using a simple randomization method. The foot massage group will receive a total of 10 sessions of foot massage over 5 weeks, with two sessions per week, while no massage intervention will be applied to the control group. All participants will be assessed at baseline, immediately after the intervention period, and two weeks following the completion of treatment. The findings of this study are expected to provide evidence regarding the effectiveness of foot massage in the management of symptoms in women with migraine.

Participants needed: 20
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Karabuk UniversityUpdated: Jun 16, 2026
Eligibility criteria

Being a woman between the ages of 18 and 45 [+4]

Having any neurological disease other than migraine [+9]

Status: Not yet recruiting

Balance, Fall Risk, and Gait in Women With Total Knee Arthroplasty

Total knee arthroplasty (TKA) is a commonly performed surgical procedure aimed at reducing pain, restoring joint function, and improving quality of life, particularly among older women. Despite improvements in pain and functional outcomes following TKA, findings regarding balance, fall risk, and gait performance remain inconsistent. Impairments in these parameters may adversely affect daily activities, independence, and overall quality of life. Unlike previous studies that have primarily focused on one or two outcomes, this study will comprehensively evaluate balance, fall risk, gait performance, and quality of life in postmenopausal women who have undergone TKA. The findings are expected to provide a more holistic understanding of long-term functional outcomes following TKA and contribute to the planning of rehabilitation programs. Therefore, the aim of this study is to compare balance, fall risk, gait performance, and quality of life between postmenopausal women who have undergone TKA and healthy postmenopausal women.

Participants needed: 30
Trial details
Age: 60-85Biological sex: FemaleType: ObservationalSponsor: Karabuk UniversityUpdated: Jun 16, 2026
Eligibility criteria

Volunteering to participate in the study. [+5]

Individuals whose vital signs are unstable after surgery, or who develop any maj... [+2]

Status: Recruiting

The Effect of Action Observation Therapy Including Unimanual and Bimanual Activities in Chronic Stroke

Functional impairments in the upper extremities following a stroke significantly restrict individuals' activities of daily living and overall quality of life; in this context, Action Observation Training (AOT) has emerged in recent years as an effective rehabilitation method that promotes motor learning processes and cortical activity by activating the mirror neuron system. Although the literature acknowledges the positive effects on neural mechanisms of both unimanuel approaches, which focus on the paretic hand alone, and bimanual approaches, which involve the simultaneous use of both hands, there remains a gap regarding which method yields superior outcomes. This study aims to compare the effectiveness of AOT interventions consisting of exclusively unimanual versus exclusively bimanual activities on upper extremity functions, activities of daily living, and quality of life in chronic stroke patients, while investigating the potential differences between the outcomes of these two distinct approaches.

Participants needed: 45
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Karabuk UniversityUpdated: Jun 9, 2026Locations: 1
Eligibility criteria

Being over 18 years of age, [+5]

Unwillingness to participate in the study, [+7]

Status: Recruiting

Action Observation Therapy in Chronic Stroke Via Telerehabilitation

Stroke, a leading cause of disability worldwide, particularly affects upper extremity function, rendering individuals dependent on others for daily living activities and reducing their quality of life. To mitigate these effects, Action Observation Therapy (AOT), which has gained prominence in recent years, activates the mirror neuron system, triggering learning processes in the motor cortex and supporting functional recovery through the imitation of observed movements. Furthermore, telerehabilitation offers a significant advantage in facilitating access to rehabilitation services for these patients requiring long-term treatment, eliminating barriers such as transportation and cost. The absence of studies in the literature comparing the effectiveness of combining these two methods on hand skills and quality of life in individuals with chronic stroke with conventional physiotherapy makes investigating the clinical value of this approach academically unique and necessary.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Karabuk UniversityUpdated: Jun 9, 2026Locations: 2
Eligibility criteria

Being over 18 years of age, [+5]

Unwillingness to participate in the study, [+7]

Status: Recruiting

Core Training in Amateur Soccer Players

The core region is a part of the body composed of axes surrounding the torso and plays a crucial role in maintaining stability. Therefore, it is considered important for maintaining athletic performance in athletes. This study aims to investigate the effects of core strength training, in addition to routine training programs, on jumping, agility, speed, balance, and shooting speed performance in amateur football players.

Participants needed: 40
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: Karabuk UniversityUpdated: May 11, 2026Locations: 1
Eligibility criteria

Being between 18-35 years old [+3]

Body mass index of 30 kg/m² or higher [+2]

Status: Not yet recruiting

Video-Supported Flipped Learning for Episiotomy Training in Midwifery Students

This study aims to evaluate the effect of a video-supported flipped learning model on anxiety and skill levels of midwifery students in episiotomy education. Episiotomy is an important clinical skill in midwifery education, and the method used to teach this skill may influence students' anxiety and performance. This randomized controlled educational study will be conducted with midwifery students who are enrolled in the episiotomy course. Participants will be randomly assigned to either an intervention group or a control group. Students in the intervention group will receive episiotomy education using a video-supported flipped learning model, in which theoretical content is provided through instructional videos prior to in-class activities. The control group will receive traditional classroom-based education. Students' anxiety levels and episiotomy skill performance will be assessed using validated measurement tools before and after the educational intervention. The findings of this study are expected to contribute to evidence-based teaching strategies in midwifery education and support the use of innovative learning models to improve student outcomes.

Participants needed: 60
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Karabuk UniversityUpdated: Apr 15, 2026
Eligibility criteria

Midwifery 3rd-year student who is taking the Normal Birth course [+3]

Incomplete completion of data collection forms [+4]

Status: Not yet recruiting

Mobile App-Supported Exercise Program For Mechanical Low Back Pain

Mechanical low back pain is one of the most common musculoskeletal disorders affecting daily activities and quality of life. Home exercise programs are frequently recommended in the management of low back pain; however, adherence to these programs is often limited. Mobile health applications may enhance adherence by providing exercise demonstrations, reminders, and monitoring tools. The aim of this study is to investigate the effects of a mobile application-supported home exercise program on posture, balance, pain, and functional status in individuals with mechanical low back pain. Participants with chronic mechanical low back pain will be randomly assigned to two groups. Both groups will receive the same home exercise program. The control group will receive the exercises in printed format, while the experimental group will follow the program through the E-Exercise mobile application that includes exercise videos, reminders, and progress tracking. Participants will be evaluated before the intervention and after six weeks of exercise training. Outcome measures will include flexibility, posture, balance, pain intensity, and functional disability. The results of this study may contribute to improving adherence to home exercise programs and promoting the use of digital health technologies in physiotherapy practice.

Participants needed: 50
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Karabuk UniversityUpdated: Apr 1, 2026
Eligibility criteria

Individuals aged between 18 and 65 years [+3]

Cauda equina syndrome [+4]

Status: Not yet recruiting

The Impact of a Infant Sleep Hygiene Training Program on Infant Sleep Habits and Parental Self-Efficacy

This randomized controlled trial aims to evaluate the effectiveness of a structured, Infant Sleep Hygiene Education Program initiated during pregnancy on infant sleep habits and parental self-efficacy related to infant sleep in the postpartum period. The program is grounded in developmental science and attachment-sensitive principles and focuses on promoting healthy sleep habits through responsive caregiving, consistent bedtime routines, and evidence-based sleep hygiene practices. Pregnant women will be randomly assigned to either an intervention group receiving a multi-session prenatal education program with postnatal follow-up support, or a control group receiving routine antenatal care. Primary outcomes include parental self-efficacy regarding infant sleep and infant sleep habits (e.g., night awakenings, sleep duration, sleep onset latency, and routine consistency), assessed at 1, 3, and 6 months postpartum. Secondary outcomes include adherence to recommended sleep-supportive parenting practices and infant sleep diary indicators. In addition, the mediating role of parental self-efficacy in the relationship between the intervention and infant sleep outcomes will be examined. Program evaluation outcomes will assess parental knowledge before and after the education, participation and adherence to the sessions, and parental satisfaction with the education program. This study aims to provide evidence for an ethical, developmentally appropriate, and preventive infant sleep education model integrated into routine prenatal care.

Participants needed: 48
Trial details
Biological sex: FemaleType: InterventionalSponsor: Karabuk UniversityUpdated: Mar 9, 2026Locations: 1
Eligibility criteria

Being a primiparous pregnant woman (first pregnancy) [+7]

The baby being born outside of the 38th to 42nd week of pregnancy [+5]

Status: Not yet recruiting

Grastion and Percussion Therapy

The study aims to investigate the effects of percussion therapy and instrument-assisted soft tissue mobilization (AISM), commonly used in clinical settings, on muscle fatigue, maximum muscle strength, pain threshold, and muscle oxygenation. The study will involve 20 volunteer participants. To achieve the study results, pre-exercise percussion therapy and instrument-assisted soft tissue mobilization (AISM) will be administered using a crossover design. Results will be measured using a digital dynamometer, a moxy oxygen monitor, and a fatigue questionnaire.

Participants needed: 20
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: Karabuk UniversityUpdated: Feb 5, 2026
Eligibility criteria

Aged 18-35 years [+3]

Upper extremity injury or surgery within the past 6 months [+7]

Status: Not yet recruiting

QR Code-Based Preoperative Education for Cesarean Birth: Anxiety, Pain, and Comfort

This study aims to evaluate the effect of QR code-based preoperative education on anxiety, postpartum pain, and comfort levels in women undergoing cesarean birth. Cesarean delivery is a common surgical procedure, and insufficient preoperative information may increase anxiety and negatively affect postoperative recovery and comfort. In this randomized controlled study, eligible pregnant women scheduled for elective cesarean birth will be assigned to either an intervention group or a control group. Women in the intervention group will receive preoperative education delivered through QR code-based digital materials, including information about the cesarean procedure, postoperative pain management, and comfort-enhancing strategies. The control group will receive routine care provided by the hospital. Anxiety levels will be assessed preoperatively, while postpartum pain and comfort levels will be evaluated after delivery using validated measurement tools. The findings of this study are expected to contribute to the development of accessible and effective educational interventions to improve maternal well-being and postoperative outcomes in cesarean birth.

Participants needed: 88
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Karabuk UniversityUpdated: Jan 26, 2026
Eligibility criteria

Pregnant women aged 18 years or older [+4]

Emergency cesarean birth or unplanned change to emergency surgery [+5]

Status: Not yet recruiting

BFR Rope Training in Male Volleyball Players

The study will be conducted during the preparatory period of the volleyball players and will span eight weeks. Throughout this period, athletes will continue their regular volleyball training four days per week, while the experimental group (n = 10) will perform rope training with blood flow restriction (BFR) twice per week, and the control group (n = 10) will perform the same rope training without BFR. Assessments will be carried out at the beginning of the 8-week period (pre-test) and at the end of the intervention (post-test). For both groups, all exercises will target the upper-extremity muscle groups. During the study, participants will be instructed to avoid consuming any medications, engaging in additional strenuous physical activities, and using any techniques or ergogenic aids that might influence the results. In both testing sessions, a standardized warm-up protocol will be implemented, consisting of a 5-minute treadmill run at 9 km/h on a Sprint Runner device (Hoggan Health Industries, Draper, UT), followed by 3 minutes of light full-body stretching. This warm-up procedure will be applied consistently across both groups to ensure standardization.

Participants needed: 26
Trial details
Age: 18-25Biological sex: MaleType: InterventionalSponsor: Karabuk UniversityUpdated: Jan 8, 2026Locations: 1
Eligibility criteria

Being healthy [+2]

Being under 18 years old [+2]

Status: Recruiting

Diaphragmatic Release for Low Back Pain

Low back pain is one of the most common musculoskeletal disorders, significantly affecting the quality of life of individuals. In non-specific low back pain, a lack of stabilization in the core region negatively impacts the performance of activities. The diaphragm forms the framework of the core region, and its dysfunction can contribute to both respiratory problems and low back pain. This study will investigate the effects of diaphragm relaxation, added to spinal stabilization exercises, on pain, disability, quality of life, central sensitization, and trunk muscle endurance.

Participants needed: 42
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Karabuk UniversityUpdated: Dec 23, 2025Locations: 1
Eligibility criteria

Being between 18-65 years of age [+2]

Psychological disorders, mental disorders, cancer, and severe depression [+4]

Status: Recruiting

Comparison of Patients With COPD and PRISM

COPD is a preventable and treatable lung disease characterized by persistent and progressive airflow limitation. PRISm, on the other hand, is a spirometry pattern that does not meet COPD diagnostic criteria despite symptoms and functional impairments, but requires maintenance. PRISm can predispose to the development of COPD and exacerbations, and can reduce exercise capacity by reducing respiratory function and oxygen consumption. There are no studies in the literature comparing respiratory muscle strength, peripheral muscle strength, and oxygenation in PRISm, COPD, and healthy individuals. Therefore, this study aimed to evaluate these parameters and compare them with healthy individuals.

Participants needed: 60
Trial details
Age: 40+Biological sex: AllType: ObservationalSponsor: Karabuk UniversityUpdated: Nov 25, 2025Locations: 1
Eligibility criteria

Being >40 years old, [+8]

Having severe orthopedic, neurological, or cardiac diseases, [+10]

Status: Recruiting

The Effects of Scapular Stabilization Exercises in Traditional Archery Athletes

This randomized controlled trial aims to investigate the effects of an 8-week scapular stabilization exercise program on shooting accuracy and upper extremity performance in athletes engaged in traditional archery. Thirty licensed archers aged between 15 and 35, with at least 2 years of experience, will be randomly assigned to an intervention group or a control group. The intervention group will receive scapular stabilization exercises in addition to their regular training, while the control group will continue their usual training routine. Pre- and post-intervention evaluations will assess upper extremity strength, stability, proprioception, and shooting performance.

Participants needed: 30
Trial details
Age: 15-35Biological sex: AllType: InterventionalSponsor: Karabuk UniversityUpdated: Jul 10, 2025Locations: 1
Eligibility criteria

Aged 15 to 35 years

History of upper extremity orthopedic surgery in the past year

Status: Recruiting

Myofascial Release Techniques in Football Players

Fascial tissue ensures optimal function and mobility by providing gliding and force transfer during movement. However, fascial order can be disrupted in cases such as overuse and trauma. Therefore, treatment of fascial tissue is important. Therefore, this study aimed to investigate the effects of different myofascial release techniques on jumping performance, flexibility, balance, and proprioception in amateur football players.

Participants needed: 48
Trial details
Age: 18-35Biological sex: MaleType: InterventionalSponsor: Karabuk UniversityUpdated: Jun 15, 2025Locations: 1
Eligibility criteria

Being between the ages of 18-35 [+3]

Those with a body mass index of 30 kg/m² or higher [+3]

Status: Recruiting

Acute Effects of Myofascial Release in Individuals With Text Neck Syndrome

This study aims to investigate the acute effects of myofascial release therapy on neck pain, functional status, and cervical range of motion in individuals diagnosed with Text Neck Syndrome (TNS). Text Neck Syndrome is increasingly prevalent due to excessive use of smartphones and other digital devices, particularly among young adults. The intervention will consist of a single session of standardized myofascial release techniques applied to the cervical and thoracic regions. The primary outcome will be neck pain intensity measured using the Numeric Rating Scale (NRS-11), while secondary outcomes will include cervical range of motion and the modified Neck Disability Index (NDI). Assessments will be performed immediately before and after the intervention. The study will be conducted with volunteer participants between the ages of 18 and 40, who use mobile devices for more than 3 hours per day and meet the diagnostic criteria for TNS

Participants needed: 20
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Karabuk UniversityUpdated: Jun 5, 2025Locations: 1
Eligibility criteria

Aged between 18 and 40 years (inclusive) [+1]

History of congenital, traumatic, or surgical pathology affecting the cervical -... [+3]

Status: Recruiting

Effectiveness of the Fascial Distortion Model in Temporomandibular Disorders: A Randomized Sham-controlled Trial

The aim of the study was to investigate the effectiveness of Manual Therapy Based on the Fascial Distortion Model in individuals with temporomandibular disorders compared to sham control. Individuals diagnosed with temporomandibular disorder will be randomly assigned to groups as Group 1 (Manual Therapy Based on Fascial Distortion Model) and Group 2 (Sham Control). Head posture, cervical and temporomandibular joint range of motion, cervical muscle performance, pain intensity, pressure pain thresholds, temporomandibular disorder severity, disability, dysfunction, health-related quality of life, kinesiophobia, and central sensitization will be assessed.

Participants needed: 30
Trial details
Age: 18-64Biological sex: AllType: InterventionalSponsor: Karabuk UniversityUpdated: Mar 12, 2025Locations: 1
Eligibility criteria

Having temporomandibular joint complaints and being diagnosed with temporomandib... [+3]

Has a systemic disease (neurological, rheumatologic, oncologic, etc.) that may a... [+6]

Status: Not yet recruiting

Model Supported Breast Examination Training for Midwifery Students

Breast cancer is the most common cancer among women worldwide and early detection significantly improves treatment success. Screening methods used for early detection include breast self-examination (BSE), clinical breast examination (CBE) and mammography. It is critical for midwifery students to learn CCM and teach this method to women. CPM allows women to recognise early signs through breast self-examination. This method is simple and inexpensive and can be applied without requiring much time and labour. Practical training of midwifery students helps them to ensure the effectiveness and correct application of this method. The use of breast examination models during the training process gives students practical experience in detecting signs of breast cancer, such as nipple depression, discharge, asymmetry of the breasts and the appearance of orange peel. In addition, midwifery students can develop their clinical skills by having the opportunity to make mistakes and gain hands-on experience in a safe environment. This process can contribute to increasing early diagnosis rates and improving treatment processes.The sample of this pre-test, post-test, follow-up randomised controlled study consisted of 64 midwifery students (experimental=32, and control=32). Data will be collected with Personal Information Form (PIF), Breast Examination Skills Assessment Form (BESAF), Self-Confidence Scale (SC) and Student Satisfaction and Confidence in Learning Scale (SCSLS). After obtaining the consent of the students in the experimental group, pre-test data will be obtained by filling out the 'Personal Information Form', 'Self-Confidence Scale' and 'Student Satisfaction and Confidence in Learning Scale'. Then, theoretical information will be given and the examination stages such as determining the area to be examined, manual examination of the area, examination method, nipple examination and detection of malignant formations in the breast will be explained practically in the breast examination model in the laboratory environment. Students will be taken in groups of 10, and after the application is explained, each student will perform the breast examination and evaluation individually. Approximately 15 minutes will be allocated for each student. Two weeks after the breast model application, the same students will be taken to the laboratory and asked to perform all the examination steps again. While the students are performing the examination steps, the researcher will mark the complete and incomplete applications on the 'Breast Examination Skill Evaluation Form' and the missing steps will be explained to the students and they will be asked to complete them. At the same time, 'Self-confidence Scale' and 'Student Satisfaction and Confidence in Learning Scale' will be filled out for the post-test. Then, two weeks later, the 'Self-Confidence Scale' and 'Student Satisfaction and Confidence in Learning Scale' will be filled out again for the final post-test. After obtaining the consent of the students in the control group, pre-test data will be collected by applying 'Personal Information Form', 'Self-Confidence Scale' and 'Student Satisfaction and Confidence in Learning Scale' to the students. Then, the students will be given theoretical information and a video will be shown to them, which includes examination stages such as determining the area to be examined, manual examination of the area, examination method, nipple examination and detection of malignant formations in the breast. Two weeks later, the students will be taken to the laboratory environment and will be asked to perform the application steps in line with the theoretical course they have taken. While the students are performing the examination steps, the researcher will mark the complete and incomplete applications on the 'Breast Examination Skill Evaluation Form', then the missing steps will be explained to the students and they will be asked to complete them. In the post-test phase, the 'Self-Confidence Scale' and the 'Student Satisfaction and Confidence in Learning Scale' will be administered to the students again. Two weeks after this process, the same scales will be filled in again for the final post-test.

Participants needed: 64
Trial details
Age: 18-25Biological sex: FemaleType: InterventionalSponsor: Karabuk UniversityUpdated: Jan 16, 2025Locations: 1
Eligibility criteria

Being a 2nd, 3rd or 4th year midwifery student at Karabük University Faculty of... [+3]

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