Clinical trials

11

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Condition / disease
Location
Status: Not yet recruiting

The Effect of Kinesio Taping Applied to the Gastrocnemius Muscle on Muscle Oxygenation, Pain Pressure Threshold, and Muscle Mechanical Properties

The aim of this study is to investigate the effects of kinesio taping applied to the gastrocnemius muscle on muscle oxygenation, pain pressure threshold, and mechanical properties of the muscle in healthy young individuals.

Participants needed: 50
Trial details
Age: 18-30Biological sex: MaleType: InterventionalSponsor: Okan UniversityUpdated: May 7, 2026
Eligibility criteria

Right lower extremity being dominant, [+1]

Having any orthopedic, neurological, circulatory, or psychiatric diagnosis, [+4]

Status: Not yet recruiting

Comparison of the Effects of Different Massage Techniques in Individuals With Bruxism

The aim of this study is to compare the effects of occlusal splint therapy and different massage techniques on pain intensity and orofacial muscle tone and stiffness in individuals with possible sleep bruxism. A secondary aim is to evaluate the effects of these interventions on oral parafunctional behaviors, disability, and sleep quality.

Participants needed: 42
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Okan UniversityUpdated: May 5, 2026
Eligibility criteria

Possible diagnosis of sleep bruxism, [+1]

Having any orthopedic, neurological, or psychiatric diagnosis, [+9]

Status: Recruiting

The Effect of the Cesarean ERAS Protocol on Mother-Infant and Father-Infant Bonding: a Multicenter, Randomized Controlled Clinical Trial.

This is a multicenter, 1:1 parallel-group, randomized controlled trial designed to compare the effect of the Enhanced Recovery After Cesarean (ERAS) protocol versus standard perioperative care on mother-infant and father-infant bonding in women undergoing cesarean delivery. The study will initially be conducted as a single-center trial at Istanbul Okan University Hospital. Once adequate site preparation is completed, additional centers will be added to expand the study to a multicenter setting. Primary Outcome: The primary outcome is the total score on the Postpartum Bonding Questionnaire (PBQ) assessed on postpartum day 7, reflecting mother-infant bonding. Secondary Outcomes: Secondary outcomes include: Maternal/Parental Postnatal Attachment Scale (MIBS) score at 2 hours postpartum (mother) PBQ score at 24 hours postpartum (mother) PBQ score at day 4 postpartum (mother) PBQ score at day 7 postpartum (father-infant bonding) Edinburgh Postnatal Depression Scale (EPDS) scores for mothers at 2 hours and 7 days postpartum Time to initiation of breastfeeding Requirement for neonatal intensive care unit (NICU) admission Sample Size: The total multicenter target sample size is n=300, with 150 participants in the ERAS group and 150 in the standard care group. The initial single-center phase at Okan University Hospital will enroll a target of n=100 participants (50 per group). Randomization: Participants will be randomized using a block and stratified randomization approach based on parity (primiparous vs multiparous) and planned type of anesthesia. Blinding (Masking): Due to the nature of the intervention, care providers cannot be blinded to group assignment. However, outcome assessors and data analysts will remain blinded to treatment allocation to minimize bias. Study Timeline and Visits: Participants will be evaluated at multiple time points following cesarean delivery: 2 hours postpartum, 24 hours postpartum, day 4 postpartum, and day 7 postpartum. All primary and secondary outcomes will be collected at the specified time points. Significance and Rationale: The ERAS protocol for cesarean delivery is designed to optimize perioperative care, enhance recovery, and potentially improve early parent-infant bonding. While previous studies have focused on maternal recovery and clinical outcomes, evidence regarding the impact of ERAS on both mother-infant and father-infant bonding remains limited. This trial aims to provide high-quality evidence on whether ERAS implementation can improve early bonding experiences, maternal mental health, breastfeeding initiation, and neonatal outcomes compared with standard perioperative care. The findings may guide future clinical practice and contribute to optimizing family-centered care in cesarean deliveries. Key Features: Multicenter, randomized controlled design Parallel 1:1 allocation Stratified randomization by parity and anesthesia type Blinded outcome assessment and data analysis Multiple postpartum evaluation points Focus on psychosocial and clinical outcomes Expected Contributions: This study will provide comprehensive data on the feasibility and effectiveness of ERAS protocols in cesarean deliveries and their potential benefits for both maternal and paternal bonding with the newborn. The inclusion of both mother-infant and father-infant outcomes, as well as maternal mental health and breastfeeding indicators, ensures a holistic assessment of early family-centered outcomes.

Participants needed: 1
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Okan UniversityUpdated: Apr 28, 2026Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

Effects of Clinical Pilates on Pain and Quality of Life in Women With Dyspareunia

The aim of this study is to investigate the effects of clinical Pilates exercises on pain, self-esteem, body image, depression, and quality of life in women with dyspareunia. The study addresses dyspareunia as a multifaceted health problem with psychological, social as well as physical implications. it evaluates the effects of pelvic floor-focused clinical Pilates interventions on physiological symptoms and psychosocial well-being. it also demonstrates this approach as effective, safe, and evidence-based method in the treatment of dyspareunia among women in Turkish society.

Participants needed: 20
Trial details
Age: 18-55Biological sex: FemaleType: InterventionalSponsor: Okan UniversityUpdated: Apr 30, 2026Locations: 1
Eligibility criteria

Female participants aged 18-55 years [+4]

Having respiratory or neurological problems [+2]

Status: Not yet recruiting

Effect of Connective Tissue Massage in Low Back Pain

Connective tissue massage (CTM) is a manual therapy method that aims to modulate the autonomic response using special stroking techniques performed on connective tissue, and its analgesic effects are described in the literature. However, studies examining the effects of CTM on multidimensional parameters such as mobility, flexibility, endurance, balance, proprioception, emotional state, and quality of life, in addition to pain and disability in chronic low back pain, are limited. This study is designed as a randomized controlled trial to evaluate the multifaceted effects of KDM applied in addition to exercise and sham massage in individuals with chronic low back pain. The study will include a total of 40 participants aged 18-65 years who have experienced low back pain for at least six months. The eight-week interventions will be conducted twice weekly; all assessments will be performed before and after treatment. The study will assess pain (VAS), functional status (RMDQ), quality of life (NHP), fatigue (FSS), sleep quality (PUKİ), lumbar mobility, flexibility, balance, core endurance, and autonomic functions.

Participants needed: 40
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Okan UniversityUpdated: Mar 10, 2026
Eligibility criteria

pregnant women, [+5]

Status: Not yet recruiting

Digital Follow-Up and Nursing Education in Bariatric Surgery Patients

This randomized controlled experimental study aims to evaluate the effect of a PHP-MySQL database-based digital follow-up system combined with structured nursing education on quality of life, body mass index (BMI), and exercise habits in patients undergoing bariatric surgery. Although bariatric surgery is an effective treatment for morbid obesity, long-term success depends largely on adherence to lifestyle modifications, including regular physical activity and sustained behavioral change. Participants will be randomly assigned to either an intervention group or a control group. The intervention group will receive structured nursing education along with an 8-week digitally monitored exercise program starting at postoperative month four. The control group will receive standard postoperative care. Outcomes will be assessed using the Moorehead-Ardelt Quality of Life Questionnaire II (MA-II), BMI measurements, and the International Physical Activity Questionnaire (IPAQ). The study aims to provide evidence for integrating digital health technologies and structured nursing interventions into postoperative bariatric care.

Participants needed: 52
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Okan UniversityUpdated: Mar 9, 2026
Eligibility criteria

Adults aged 18-65 years Undergoing bariatric surgery Eligible for physical activ...

Severe cardiopulmonary disease or any medical condition that contraindicates exe...

Status: Not yet recruiting

THE RELATIONSHIP BETWEEN PAIN ANXIETY AND POST-OPERATIVE PAIN IN PATIENTS UNDERGOING CHOLECYSTECTOMY SURGERY

This descriptive observational study aims to examine the relationship between preoperative fear of postoperative pain and postoperative pain intensity in patients undergoing cholecystectomy. Postoperative pain is one of the most common and significant clinical problems following surgical procedures. Psychological factors such as anxiety and fear of pain are known to influence pain perception and recovery outcomes. Preoperative fear related to postoperative pain may increase perceived pain intensity and negatively affect the postoperative recovery process. The study will be conducted in the general surgery clinics of a tertiary care hospital. A total of 106 adult patients scheduled for cholecystectomy will be included. Preoperative fear of postoperative pain will be assessed one day before surgery using the Postoperative Pain Fear Scale. Postoperative pain intensity will be evaluated using the Numeric Rating Scale at the 4th, 12th, and 24th hours after surgery. The findings of this study are expected to contribute to a better understanding of the relationship between preoperative pain-related fear and postoperative pain severity, and to provide evidence to improve perioperative nursing care and pain management strategies.

Participants needed: 106
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Okan UniversityUpdated: Mar 9, 2026Locations: 1Duration: 106 Years
Eligibility criteria

Adults aged 18 years and older Scheduled for elective cholecystectomy Able to sp...

Use of anxiolytic medication Diagnosed psychiatric disorder that may affect pain...

Status: Not yet recruiting

Exercise Program Combined With Ergonomic Training in Textile Workers

Most studies in the literature focus on musculoskeletal disorders and pain levels in occupational groups with repetitive workloads, such as textile workers. However, due to the nature of the work environment, decreased respiratory function and postural disorders are also frequently observed in these individuals. There is no comprehensive study in the literature that combines respiratory exercises, posture training, and ergonomics training for textile workers. Therefore, this study will examine the effects of a regular exercise program implemented alongside ergonomics training provided to textile workers on respiratory parameters, musculoskeletal disorders, posture, functionality, pain levels, and fatigue intensity.

Participants needed: 60
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Okan UniversityUpdated: Feb 13, 2026
Eligibility criteria

Individuals with orthopedic or neurological conditions that prevent exercise, [+2]

Status: Not yet recruiting

Blood Flow Technique Effect on the Muscle Mechanics

This study will be a study in which we take measurements with the myotonPRO device to determine whether the resistant exercises performed without the blood flow restrictive technique and with the blood flow restrictive technique affect the biceps muscle of the participants, who were divided into groups by randomization method after determining the 1 max repetition you can lift.

Participants needed: 57
Trial details
Age: 18-25Biological sex: AllType: ObservationalSponsor: Okan UniversityUpdated: Mar 6, 2025
Eligibility criteria

Being a healthy male or female volunteer between 18 and 35 (who has not particip... [+1]

Having a history of biceps musculoskeletal injury. [+3]

Status: Not yet recruiting

Comparison of the Effects of Intermittent Pneumatic Compression, Graston Technique and Percussive Therapy

The aim of this study was to compare the effects of intermittent pneumatic pressure, percussive therapy and graston after a fatigue protocol applied to the leg muscles.

Participants needed: 60
Trial details
Age: 25-45Biological sex: AllType: InterventionalSponsor: Okan UniversityUpdated: Oct 15, 2024Locations: 1
Eligibility criteria

To be between 25-45 years old. [+6]

Having a chronic disease. [+6]

Status: Not yet recruiting

The Effect of Kamishibai Diabetes Education on Knowledge, HbA1c, and Quality of Life in Children

Children diagnosed with Type 1 Diabetes Mellitus (T1DM) initially receive intensive education with their families. Studies indicate that over time, this initial education becomes routine, reducing its effectiveness and failing to adequately address developmental stages, thus requiring repetition. Current methods involve long and intensive educational sessions in hospitals using the Childhood Diabetes Education Guide. These extended, non-interactive sessions often lead to a loss of motivation, decreased learning efficiency, and negative attitudes among patients and their families. This study aims to develop an educational tool utilizing the Kamishibai method specifically for children with T1DM aged 8-12. The Kamishibai method is designed to align with their cognitive and sensory development, promoting effective and engaging learning experiences for diabetic patients. By incorporating interactive and visually stimulating elements, Kamishibai seeks to enhance motivation and retention of diabetes education. Hypothesis 1: Children diagnosed with Type 1 DM have higher knowledge levels in the group educated with the Kamishibai method compared to those receiving routine education. Hypothesis 2: The Hemoglobin A1c parameter is lower in the Kamishibai-educated group. Hypothesis 3: The quality of life is higher in the Kamishibai-educated group. This study will assess the effectiveness of the Kamishibai method by comparing it to routine educational approaches. The detailed protocol includes technical aspects of the intervention, measurement tools, data collection methods, and statistical analysis plans to ensure a comprehensive evaluation of the method's impact on knowledge levels, HbA1c parameters, and quality of life.

Participants needed: 60
Trial details
Age: 8-12Biological sex: AllType: InterventionalSponsor: Okan UniversityUpdated: Aug 2, 2024Locations: 1
Eligibility criteria

The child is 8-12 years old. [+4]

Presence of another chronic disease other than T1DM that may affect glycemic con... [+4]