[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Gaziantep Islam Science and Technology University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":240},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,45,79,106,133,165,193,216],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100643979","effects-of-hybrid-family-planning-counseling-on-postpartum-maternal-health-100643979",false,"NCT07667374","Effects of Hybrid Family Planning Counseling on Postpartum Maternal Health","THE EFFECTS OF HYBRID FAMILY PLANNING COUNSELING IN THE POSTPARTUM PERIOD ON MATERNAL HEALTH: A LONGITUDINAL STUDY","Inclusion Criteria:\n\n* Being over 18 years old Not having received family planning counseling before Being pregnant for the first time Being able to use technological\u002Fonline systems and having a communication device that can install these systems (smartphone, messaging, Google Forms, Zoom, WhatsApp) Not having vision or hearing problems Being able to read and write Being in the last trimester (34 weeks of pregnancy or more)\n\nExclusion Criteria:\n\n* The mother having a condition that prevents her from using family planning methods (reproductive organ conditions, hormonal disorders, etc.) Having been diagnosed with a chronic or psychological disorder (cardiovascular diseases, depression, epilepsy, asthma, etc.).","FEMALE","18 Years",{"count":19,"type":20},96,"ESTIMATED","INTERVENTIONAL",[23],"NA","This research aims to examine the effects of hybrid family planning counseling on maternal health in the postpartum period. The study is unique and innovative in that it evaluates the effectiveness of hybrid counseling models, which are gaining importance in the literature but have been the subject of a limited number of studies, particularly in Turkey. The World Health Organization recommends a minimum interval of 24 months between births, and it is known that early postpartum pregnancies have negative effects on maternal and neonatal health. In this context, the hybrid family planning counseling model to be developed will contribute to reducing maternal mortality and morbidity by supporting women in making informed and correct contraceptive choices. Furthermore, it is predicted that the findings of the study will be directly related to the United Nations Sustainable Development Goals, namely gender equality, healthy living, and quality education. The research is planned as a randomized controlled longitudinal study. Data collection is planned for August 2026 at the Adana City Training and Research Hospital antenatal clinic. The sample will consist of a total of 96 pregnant women, 48 in the experimental group and 48 in the control group, determined by power analysis. A counseling module will be created by gathering expert opinions. The module will consist of 3 sessions. Each session will last 45 minutes, including 30 minutes of interactive presentation and 15 minutes of question and answer. The module sessions will have a dynamic structure that takes into account the needs of the mother during pregnancy and the postpartum period. The first meeting will be held face-to-face in the hospital at 34-38 weeks of pregnancy, the second meeting will be online within the first 4 weeks postpartum, and the third meeting will be online at 6 weeks postpartum. During the implementation phase, quantitative measurements of the research will be carried out using the \"Antenatal Pregnancy Information Form\", \"Postnatal Mother Information Form\", \"Postpartum Family Planning Attitude Scale\", \"Edinburgh Postpartum Depression Scale\" and \"Sexual Life Quality Scale\".\n\nResearch hypotheses:\n\nH0: Longitudinal hybrid family planning counseling (antenatal-postpartum period) does not affect maternal health. H1: Longitudinal (antenatal-postpartum) hybrid family planning counseling affects maternal health.",[26],"Postpartum Family Planning Counseling",[28,29,30,31],"Family planning","Maternal health","Postpartum","Hybrid counseling","NOT_YET_RECRUITING","2026-06-18",{"date":35,"type":36},"2026-06-25","ACTUAL",{"date":38,"type":20},"2026-08",{"date":40,"type":20},"2028-04",{"name":42,"class":43},"Gaziantep Islam Science and Technology University","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":52,"sex":53,"minAge":54,"maxAge":17,"enrollmentInfo":55,"targetDuration":4,"studyType":21,"phases":57,"briefSummary":58,"conditions":59,"keywords":66,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":44},"100641968","the-effects-of-game-based-exercise-programs-100641968","NCT07660822","THE EFFECTS OF GAME-BASED EXERCISE PROGRAMS","THE EFFECTS OF VIRTUAL REALITY AND VIDEO GAME-BASED EXERCISE PROGRAMS ON PHYSICAL FITNESS AND ATTENTION LEVELS IN HEALTHY ADOLESCENTS","Inclusion Criteria:\n\n* Volunteering to participate in the study\n* Being an adolescent aged 10-18 years\n* Having a score below 4 on the Physical Activity Scale for Adolescents\n\nExclusion Criteria:\n\n* Having any physical disability that would prevent participation in the exercise program\n* Having upper or lower extremity orthopedic disease\n* Having a score above 4 on the Physical Activity Scale for Adolescents",true,"ALL","10 Years",{"count":56,"type":20},48,[23],"Studies comparing aerobic exercise with virtual reality or video game technologies to traditional games and classical exercise have been conducted in healthy adolescents, but no studies comparing virtual reality and video game technologies have been found. Based on all this, we aimed to investigate the effect of virtual reality and video game-based exercise programs on physical fitness and attention levels in healthy adolescents. The study was planned as a quantitative experimental randomized controlled trial. Healthy individuals aged 10-18 years who meet the inclusion criteria will be evaluated during the dates of the study. Individuals will be divided into 3 groups: a classical physical activity group, a virtual reality group, and a video-based game group. Each program will be implemented for 20-30 minutes, three days a week for eight weeks. The Physical Activity Scale for Adolescents was used to evaluate the physical activity of the individuals, the Multidimensional Body-Self Relationship Scale was used to measure body image, and the Exercise Benefit\u002FBarrier Scale was used to measure exercise perception. To measure attention, balance, and reaction time, the D2 Attention Test, Y-Balance Test, and Nelson's Hand Reaction Test will be administered, respectively. In the virtual reality and video-based game group, the games played by participants will be similar to the physical activities performed in the classic exercise group. One or more games incorporating these physical activities will be selected.",[60,61,62,63,64,65],"Physical Activity","Body Image","Exercise Perception","Balance","Reaction Time","Attention",[67,68,69],"Healthy adolescent","virtual reality","attention level)","RECRUITING","2026-06-16",{"date":73,"type":36},"2026-06-22",{"date":75,"type":36},"2025-11-15",{"date":77,"type":20},"2026-08-30",{"name":42,"class":43},{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":4,"eligibilityCriteria":85,"healthyVolunteers":52,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":86,"targetDuration":4,"studyType":21,"phases":87,"briefSummary":88,"conditions":89,"keywords":93,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":44},"100641431","the-effect-of-skin-to-skin-contact-at-birth-100641431","NCT07656207","The Effect of Skin-to-skin Contact at Birth","The Effect of Skin-to-skin Contact at Birth on Birth Outcomes and Parenting Behavior","Inclusion Criteria:\n\n* Vaginal delivery\n* Primiparous pregnancy\n* Delivery at 37 weeks or later\n* Single, live fetus\n* Not a high-risk pregnancy\n* Not an individual with special needs\n* Able to communicate\n\nExclusion Criteria:\n\n* Women who Have a multiple pregnancy,\n* Develop complications requiring emergency intervention in the mother or baby after delivery,\n* Have their baby admitted to the neonatal intensive care unit after delivery,\n* Have a cesarean section,\n* Withdraw from the study will be excluded from the research.",{"count":19,"type":20},[23],"To determine the effects of skin-to-skin contact at birth on birth outcomes (placental delivery time, postpartum pain level, time of first breastfeeding, and breastfeeding motivation) and on postpartum parenting behavior.",[90,91,92],"Midwifery Support","Skin to Skin Contact","Parenthood Status",[94,95,96,97,98],"Skin to skin","pain","breastfeeding","parenthood","midwifery","2026-06-14",{"date":33,"type":36},{"date":102,"type":20},"2026-07",{"date":104,"type":20},"2027-06",{"name":42,"class":43},{"id":107,"slug":108,"hasResults":11,"nctId":109,"briefTitle":110,"officialTitle":111,"acronym":4,"eligibilityCriteria":112,"healthyVolunteers":11,"sex":53,"minAge":17,"maxAge":4,"enrollmentInfo":113,"targetDuration":4,"studyType":115,"phases":4,"briefSummary":116,"conditions":117,"keywords":122,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":125,"lastUpdatePostDateStruct":126,"startDateStruct":128,"completionDateStruct":130,"leadSponsor":132,"locationsCount":4},"100631949","turkish-version-of-the-neurogenic-bladder-symptom-score-short-form-100631949","NCT07507331","Turkish Version of the Neurogenic Bladder Symptom Score Short Form","Turkish Version of the Neurogenic Bladder Symptom Score Short Form: Cross-Cultural Adaptation and Validation-Reliability Study","Inclusion Criteria:\n\n* Being ≥18 years old\n\n  * Having a diagnosis of Spinal Cord Injury (SCI) or Multiple Sclerosis (MS) and neurogenic lower urinary tract dysfunction\n  * Being able to read and understand Turkish and have the cognitive ability to independently complete questionnaires\n  * Can be included with any bladder management method (spontaneous voiding, CIC, permanent catheter, condom catheter, reconstruction\u002Fdiversion etc.)\n  * Volunteering and signing informed consent\n\nExclusion Criteria:\n\n* Having an active urinary tract infection (UTI)\n* Having undergone urological surgery in the last month\n* Reporting changes in bladder\u002Furinary function between the first and second applications (surgery, UTI, change in bladder medication)\n* Having a significant recent change in general health status\n* Having a spinal cord injury (SCI) in the spinal shock phase\n* Having experienced a relapse of Multiple Sclerosis (MS) within the last 3 months.",{"count":114,"type":20},120,"OBSERVATIONAL","This observational study aims to evaluate the cross-cultural adaptation and psychometric properties of the Turkish version of the Neurogenic Bladder Symptom Score Short Form (NBSS-SF) in adults with spinal cord injury or multiple sclerosis who have neurogenic lower urinary tract dysfunction. Neurogenic bladder symptoms, such as urinary incontinence, urgency, and difficulties with urine storage or emptying, may negatively affect daily functioning and quality of life. In this study, the validity and reliability of the Turkish NBSS-SF will be examined, and convergent validity will be assessed through its relationship with the King's Health Questionnaire (KHQ) and the Short Form-12 (SF-12). In eligible participants, the scale will be administered again after 7 to 14 days. The aim of the study is to provide a valid and reliable Turkish patient-reported outcome measure for use in clinical practice and research.",[118,119,120,121],"Neurogenic Bladder Disorder","Spinal Cord Injury","Multiple Sclerosis","Lower Urinary Track Symptoms",[123,124,119,120],"Neurogenic Bladder","Neurogenic Bladder Symptom Score- Short Form Validation","2026-04-07",{"date":127,"type":36},"2026-04-13",{"date":129,"type":20},"2026-03-27",{"date":131,"type":20},"2026-05",{"name":42,"class":43},{"id":134,"slug":135,"hasResults":11,"nctId":136,"briefTitle":137,"officialTitle":137,"acronym":4,"eligibilityCriteria":138,"healthyVolunteers":52,"sex":139,"minAge":140,"maxAge":141,"enrollmentInfo":142,"targetDuration":4,"studyType":21,"phases":144,"briefSummary":145,"conditions":146,"keywords":152,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":157,"lastUpdatePostDateStruct":158,"startDateStruct":160,"completionDateStruct":162,"leadSponsor":164,"locationsCount":44},"100615671","mobile-prenatal-education-for-expectant-fathers-and-its-effects-on-bonding-stress-breastfeeding-and-marital-satisfaction-100615671","NCT07295639","Mobile Prenatal Education for Expectant Fathers and Its Effects on Bonding, Stress, Breastfeeding and Marital Satisfaction","Inclusion Criteria:\n\n* Age between 19 and 65 years\n* First-time father\n* Has become a father within the last month\n* Has a healthy newborn without congenital anomalies or chronic illnesses\n* Does not have a premature or low-birth-weight baby\n* Has not become a father through adoption\n* Owns a mobile phone capable of accessing the mobile-based application\n* Has an Android or iOS operating system\n* Has not received any infant care training within the last 6 months\n* Has no physical or mental disability that would prevent viewing, hearing, or understanding the research questions or educational content\n* Voluntarily agrees to participate in the research\n\nExclusion Criteria:\n\n* Declines to participate in the research\n* Does not own a smartphone\n* Cannot use mobile applications\n* Has a physical or mental condition that prevents completing the questionnaires\n* Has a baby with congenital anomalies or chronic medical conditions\n* Has a premature or low-birth-weight baby\n* Has received infant care training within the last 6 months\n* Has adopted a child\n* Is outside the 19-65 age range","MALE","19 Years","65 Years",{"count":143,"type":20},80,[23],"The aim of this interventional clinical trial is to assess whether a mobile-based antenatal education programme for expectant fathers has a positive effect on father-infant bonding, stress levels, and breastfeeding attitudes.\n\nThe study aims to answer the following main questions:\n\nDoes participation in a mobile-based prenatal education programme strengthen fathers' emotional bonds with their babies? Does the education reduce fathers' stress levels during the prenatal and postnatal periods? Does it increase the father's knowledge and supportive attitude towards breastfeeding? Researchers will compare whether there are measurable differences in attachment, stress, and breastfeeding attitudes between the intervention group (fathers receiving mobile-based education) and the control group (fathers receiving standard routine information).\n\nParticipants: Will complete pre- and post-intervention questionnaires assessing attachment, stress, and breastfeeding attitudes.\n\nThe intervention group will have access to a six-module mobile application covering topics such as infant care, nutrition, sleep routines, health and safety, emotional development, and daily care practices.\n\nThe study will be conducted with fathers aged 19-65 who became fathers within the last month and voluntarily agreed to participate.",[147,148,149,150,151],"Breastfeeding Attitudes","Breast Feeding","Paternal Behavior","Health Education","Parent-Child Relations",[153,154,155,156],"father-infant bonding","paternal stress","breastfeeding attitudes","mobile-based education","2025-12-16",{"date":159,"type":36},"2025-12-19",{"date":161,"type":20},"2026-01",{"date":163,"type":20},"2026-10",{"name":42,"class":43},{"id":166,"slug":167,"hasResults":11,"nctId":168,"briefTitle":169,"officialTitle":170,"acronym":4,"eligibilityCriteria":171,"healthyVolunteers":11,"sex":53,"minAge":172,"maxAge":173,"enrollmentInfo":174,"targetDuration":4,"studyType":115,"phases":4,"briefSummary":176,"conditions":177,"keywords":179,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":185,"lastUpdatePostDateStruct":186,"startDateStruct":188,"completionDateStruct":190,"leadSponsor":192,"locationsCount":4},"100604872","backward-walking-and-related-factors-in-individuals-with-stroke-100604872","NCT07155161","Backward Walking and Related Factors in Individuals With Stroke","Relationship Backwalking Ability and Lower Extremity Function, Proprioception, Trunk Control, And Balance Iduals With Stroke","Inclusion Criteria:\n\n* who can walk 10 meters without physical assistance,\n* Lower extremity functions are in stages 2-6 of the Brunnstrom motor recovery scale,\n* Have been at least 3 days and no more than 24 months post-stroke,\n* Scored 24 or higher on the Mini Mental Test\n\nExclusion Criteria:\n\n* Individuals with neurological or orthopedic problems other than stroke that affect walking,\n* A history of cardiovascular or rheumatological diseases that interfere with daily activities,\n* A lower extremity lesion or fracture,\n* Lower extremity spasticity of 4 on the Modified Ashworth Scale (MAS),\n* Aphasia or communication disorders","30 Years","85 Years",{"count":175,"type":20},30,"Objective: To examine the relationship between backward walking ability and lower extremity function, proprioception, trunk control, and balance in individuals with stroke. Thirty individuals aged 30-85 who have had a stroke will be included in our study. Individuals with stroke who can walk 10 m without physical assistance, whose lower extremity functions are in the Brunnstrom motor recovery stages 2-6, who have been post-stroke for at least 3 days and up to 24 months, and who score 24 or higher on the Mini Mental Test will be included. Demographic information of individuals with stroke who meet the inclusion criteria will be recorded in a personal information form. Lower extremity function will be evaluated with the 3-meter back walking test (3MGYT), proprioception with the Fugl Meyer lower extremity assessment scale, with a digital goniometer, trunk control with the Trunk Impairment scale, and balance with the Brief BESTTest.",[178],"Stroke",[180,181,182,183,184],"stroke","back ward walking","proprioception","trunk control","balance","2025-09-05",{"date":187,"type":36},"2025-09-08",{"date":189,"type":20},"2025-09-15",{"date":191,"type":20},"2026-09-25",{"name":42,"class":43},{"id":194,"slug":195,"hasResults":11,"nctId":196,"briefTitle":197,"officialTitle":198,"acronym":4,"eligibilityCriteria":199,"healthyVolunteers":11,"sex":53,"minAge":200,"maxAge":4,"enrollmentInfo":201,"targetDuration":4,"studyType":115,"phases":4,"briefSummary":203,"conditions":204,"keywords":206,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":185,"lastUpdatePostDateStruct":210,"startDateStruct":212,"completionDateStruct":213,"leadSponsor":215,"locationsCount":4},"100604901","bed-bridge-test-in-acute-stroke-patients-100604901","NCT07155538","Bed Bridge Test in Acute Stroke Patients","Validity and Reliability of the Bed Bridge Test in Acute Stroke Patients","Inclusion Criteria:\n\n* medically stable\n* ischemic or hemorrhagic stroke within six months.\n* 40 years of age or older,\n* have no other known neurological or orthopedic problems,\n* have a Mini Mental Test score of 24 or higher.\n\nExclusion Criteria:\n\n-diagnosed with cognitive impairment and those with communication and cooperation problems","40 Years",{"count":202,"type":20},50,"Studies examining the validity and reliability of easy-to-apply muscle strength and mobility outcome measures in the acute and subacute phases of stroke are quite limited. Therefore, the purpose of this study was to investigate whether the In-Bed Bridge Test is a useful outcome measure for assessing lower extremity muscle strength and mobility in stroke.",[205],"Stroke, Acute",[180,207,208,209],"validity","reliability","bed bridge test",{"date":211,"type":36},"2025-09-11",{"date":189,"type":20},{"date":214,"type":20},"2026-03-25",{"name":42,"class":43},{"id":217,"slug":218,"hasResults":11,"nctId":219,"briefTitle":220,"officialTitle":221,"acronym":4,"eligibilityCriteria":222,"healthyVolunteers":11,"sex":53,"minAge":17,"maxAge":223,"enrollmentInfo":224,"targetDuration":4,"studyType":115,"phases":4,"briefSummary":225,"conditions":226,"keywords":228,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":232,"lastUpdatePostDateStruct":233,"startDateStruct":235,"completionDateStruct":237,"leadSponsor":239,"locationsCount":44},"100528134","turkish-lower-extremity-motor-activity-log-le-mal-100528134","NCT06156813","Turkish Lower-Extremity Motor Activity Log (LE-MAL)","Validity and Reliability of Turkish Version of the Lower Extremity Motor Activity Log","Inclusion Criteria:\n\n* Individuals between the ages of 18-80 living in Gaziantep who applied to the neurology outpatient clinic of Hospital and were diagnosed with stroke.\n\nExclusion Criteria:\n\n* Patients with a history of trauma within the last year, alcohol and substance addiction, and pregnancy","80 Years",{"count":143,"type":20},"The Motor Activity Log was developed to measure paretic upper extremity use in daily activities in the real-life context (real world) of people with different health conditions, including stroke. Subsequently, the Lower Extremity Motor Activity Diary was developed. This survey is a semi-structured survey in which the participant is asked to rate himself\u002Fherself according to each scale over 14 activities.",[178,227],"Spastic Paraplegia",[229,230,231,207,208],"LE-MAL","Spasticity","Measurement","2025-03-06",{"date":234,"type":36},"2025-03-11",{"date":236,"type":36},"2023-11-15",{"date":238,"type":20},"2025-12-15",{"name":42,"class":43},""]