[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"young-adult-females\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:young-adult-females":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,44,77,112],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100641580","effects-of-passive-recovery-methods-after-high-intensity-cycling-exercise-100641580",false,"NCT07652398","Effects of Passive Recovery Methods After High-Intensity Cycling Exercise","Acute Effects of Five Passive Recovery Interventions Following High-Intensity Cycling Exercise: A Randomized Five-Period Crossover Trial","RECOVER-CYCLE","Inclusion Criteria:\n\n* Healthy adult volunteers aged 18-35 years\n* Able to perform high-intensity cycling exercise\n* No musculoskeletal injury within the last six months\n* No known cardiovascular, neurological, or metabolic disease\n* Not using medication that may affect exercise performance, pain perception, or recovery\n* Willing to attend all five study sessions\n* Willing to receive all five passive recovery interventions\n* Provided written informed consent\n\nExclusion Criteria:\n\n* Presence of acute or chronic musculoskeletal injury\n* History of cardiovascular, neurological, respiratory, or metabolic disease\n* Contraindication to high-intensity exercise\n* Contraindication to compression therapy, vacuum therapy, kinesiology taping, passive rest, or classical massage\n* Skin allergy, open wound, dermatological disease, or sensitivity to kinesiology tape\n* Use of analgesic, anti-inflammatory, muscle relaxant, or performance-enhancing medication during the study period\n* Participation in another exercise or recovery intervention study during the study period\n* Failure to attend all study sessions or comply with study procedures",true,"ALL","18 Years","30 Years",{"count":22,"type":23},10,"ESTIMATED","INTERVENTIONAL",[26],"NA","This randomized crossover trial will investigate the acute effects of five passive recovery interventions following a standardized high-intensity cycling exercise protocol. Participants will complete one supervised high-intensity cycling session per week for five consecutive weeks. Immediately after each exercise session, participants will receive one of five recovery interventions: compression therapy, vacuum therapy, kinesiology taping, passive rest, or classical massage. The order of the interventions will be randomized according to a balanced crossover sequence. Each participant will experience all five recovery interventions during the study period. Outcomes related to post-exercise recovery will be assessed across intervention periods.",[29,30],"Young Adult Health","Young Adult Females","RECRUITING","2026-06-26",{"date":34,"type":35},"2026-06-30","ACTUAL",{"date":37,"type":35},"2026-06-22",{"date":39,"type":23},"2027-08-28",{"name":41,"class":42},"Pamukkale University","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":17,"sex":51,"minAge":19,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":24,"phases":55,"briefSummary":56,"conditions":57,"keywords":61,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":43},"100640077","trauma-informed-yoga-intervention-in-young-women-100640077","NCT07589777","Trauma-Informed Yoga Intervention in Young Women","Trauma-Informed Yoga Intervention: A Randomized Controlled Trial on Psychological Trauma, Emotion Regulation, and Interoceptive Awareness in Young Adult Women","Inclusion Criteria:\n\n* Being a woman aged 18-25 years\n* Providing voluntary written informed consent after being informed about the study\n* Scoring within the highest 25th percentile on the Transmitted Psychological Trauma Scale based on the pre-screening assessment, indicating high levels of trauma-related symptoms\n* Having no physical limitations that would prevent participation in weekly sessions and being medically eligible to engage in yoga practices\n* Agreeing to comply with the study protocol, including attendance at intervention sessions and completion of all assessments\n\nExclusion Criteria:\n\n* Inability to provide reliable responses due to the presence of active psychotic disorder, bipolar disorder, or severe cognitive impairment\n* Being in an acute psychological crisis\n* Initiation of intensive psychotherapy targeting trauma symptoms (e.g., trauma-focused therapy) within the past 3 months or participation in a similar structured psychosocial intervention during the study period\n* Presence of serious musculoskeletal, cardiovascular, or neurological conditions or injuries that would prevent participation in yoga, or medical restriction of physical activity by a physician\n* Having an established regular practice of yoga or meditation","FEMALE","25 Years",{"count":54,"type":23},46,[26],"The aim of this study is to evaluate the effects of a trauma-informed yoga intervention on psychological trauma symptoms, difficulties in emotion regulation, and interoceptive awareness in young adult women.",[58,30,59,60],"Trauma","Awareness","Emotional Regulation",[62,63,64,65,66],"trauma-informed yoga","emotion regulation","interoceptive awareness","psychological trauma","randomized controlled trial","NOT_YET_RECRUITING","2026-05-09",{"date":70,"type":35},"2026-05-15",{"date":72,"type":23},"2026-06-01",{"date":74,"type":23},"2026-11-30",{"name":76,"class":42},"Saglik Bilimleri Universitesi",{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":11,"sex":51,"minAge":19,"maxAge":84,"enrollmentInfo":85,"targetDuration":4,"studyType":87,"phases":4,"briefSummary":88,"conditions":89,"keywords":91,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":43},"100590390","sexual-functon-in-young-women-after-breast-cancer-surgery-100590390","NCT06966791","Sexual Functıon in Young Women After Breast Cancer Surgery","Examınatıon of Sexual Functıon in Young Women After Breast Cancer Surgery","Inclusion Criteria:\n\n* Individuals scheduled for surgery for breast cancer\n* Accepting to participate in the study\n* Being sexually active in the last 1 year\n* Continuation of menstruation\n\nExclusion Criteria:\n\n* Previous breast cancer surgery\n* Previous history of breast cancer\n* History of any other cancer\n* Refusal to participate in the study\n* Refusal to continue working\n* Problems in her relationship with her partner","50 Years",{"count":86,"type":23},52,"OBSERVATIONAL","The aim of this observational study was to analyse sexual function in young women after breast cancer surgery. The main question it aims to answer is Sexual function in young women after breast cancer surgery changes during the one-year follow-up period. Participants will answer demographic information, Female Sexual Function Scale, Breast-Q and Body Perception Scale about their sexual function, quality of life and body perception. These will be recorded before surgery and repeated 6 weeks, 6 months and 1 year after surgery.",[90,30],"Breast Cancer Surgery",[92,93,94,95,96,97,98,99,100,101,102],"sexual functions","breast cancer surgery","young adult females","Breast Cancer Treatment","quality of life","breast cancer survival","body perception","Mastectomy","Mastectomy, Modified Radical","Mastectomy, Segmental","breast conserving surgery","2026-02-19",{"date":105,"type":35},"2026-02-20",{"date":107,"type":35},"2024-12-30",{"date":109,"type":23},"2026-07-25",{"name":111,"class":42},"ATİYE KAŞ ÖZDEMİR",{"id":113,"slug":114,"hasResults":11,"nctId":115,"briefTitle":116,"officialTitle":117,"acronym":4,"eligibilityCriteria":118,"healthyVolunteers":17,"sex":51,"minAge":119,"maxAge":120,"enrollmentInfo":121,"targetDuration":4,"studyType":24,"phases":122,"briefSummary":123,"conditions":124,"keywords":128,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":138,"lastUpdatePostDateStruct":139,"startDateStruct":141,"completionDateStruct":143,"leadSponsor":145,"locationsCount":43},"100601564","non-diet-nutrition-education-and-its-effects-on-eating-behavior-body-image-and-well-being-in-adult-women-100601564","NCT07112131","Non-Diet Nutrition Education and Its Effects on Eating Behavior, Body Image, and Well-Being in Adult Women","The Effect of Non-Diet Nutrition Education on Eating Behavior, Body Image, and Well-Being in Adult Women: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Female,\n* Aged between 19-35 years,\n* Body Mass Index (BMI) between 18.5-24.9,\n\nExclusion Criteria:\n\n* Pregnant or breastfeeding,\n* Diagnosed eating disorder or other psychiatric condition,\n* Currently enrolled in a weight loss program,\n* Following a restrictive diet due to medical conditions.","19 Years","35 Years",{"count":86,"type":23},[26],"The goal of this clinical trial is to evaluate whether a non-diet nutrition education program can improve eating behaviors, body image, and well-being in normal-BMI women aged 19-35 years. The main questions it aims to answer are:\n\n* Does participation in an 8-week non-diet nutrition education program improve eating behavior, body image, and well-being over time in the intervention group compared to the control group?\n* Is there a significant difference between the intervention and control groups in eating behavior, body image, and well-being after the intervention?\n\nResearchers will compare an intervention group receiving an 8-week non-diet nutrition education with a control group receiving no intervention, to see if the program leads to improvements in psychological and behavioral outcomes without focusing on weight loss.\n\nParticipants will:\n\n* Complete pre- and post-intervention assessments, including validated questionnaires on eating behavior (DEBQ, FCQ, IES-2), body image (BAS, Stunkard Figure Rating Scale), and psychological well-being (WHO-5, Rosenberg Self-Esteem Scale), as well as a 3-day food diary.\n* Be randomly assigned to either the intervention group (8-week online non-diet nutrition education sessions) or the control group (no intervention).\n* Engage in 8 weekly, 60-minute sessions focused on intuitive eating, body acceptance, and health-promoting nutrition.",[125,126,127,30],"Eating Behaviors","Body Image","Well-Being, Psychological",[129,130,131,132,133,134,135,136,137],"Non-diet approach","Intuitive eating","Body acceptance","Body image","Eating behavior","Psychological well-being","Young adult women","Nutrition education","Randomized controlled trial","2025-08-01",{"date":140,"type":35},"2025-08-08",{"date":142,"type":35},"2025-07-21",{"date":144,"type":23},"2025-10",{"name":146,"class":42},"Tuğba TÜRKCAN"]