[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"strength\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:strength":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,44,80,107,145,175],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100641159","dry-needling-and-quad-strength-after-anterior-cruciate-ligament-reconstructon-100641159",false,"NCT07657195","Dry Needling and Quad Strength After Anterior Cruciate Ligament Reconstructon","Effects of Dry Needling on Quadriceps Muscle Strength in Acute Post-Operative Anterior Cruciate Ligament Reconstruction With Quadriceps Autograft in the Pediatric Population.","ACLR","Inclusion Criteria:\n\n* Status post subacute quadriceps autograft 6 weeks or less\n* Ages 10-20 years\n* English and\u002For Spanish speaking\n\nExclusion Criteria:\n\n* History of surgery on the knee or hip on the testing lower extremity.\n* Any surgical intervention to other ligamentous or meniscus structures during time of ACLR\n* Any post-surgical complications such as infection\n* Current pregnancy","ALL","10 Years","20 Years",{"count":21,"type":22},40,"ESTIMATED","INTERVENTIONAL",[25],"NA","Dry needling is a skilled intervention provided by trained physical therapists to treat pain, myofascial dysfunction, and a variety of other diagnosis. While there is research demonstrating the benefits of dry needling in reduction of pain and improvement in strength, research in regards the pediatric population is very limited. I recently completed a retrospective chart review regarding dry needling trends and outcomes in the pediatric orthopedic population. We now know the pediatric population is tolerating this treatment and seeing benefits. Physical therapists are already pushing the boundaries and finding additional benefits in the use of dry needling with our current patients. A diagnosis frequently seen in sports medicine is surgical reconstruction of the anterior cruciate ligament (ACL). Over the last couple of years, therapists have seen an increase in the use of quadriceps tendon autograft for reconstruction following ACL tears due to lower incidence rate of retears. These patients have been struggling to regain strength of the quadriceps to meet desired outcomes. The quadricep muscles are one of the major stabilizers of the knee and with a reduction in strength places the patient at a significant increase of retear.\n\nSubjects will be categorized into an experimental group (dry needling intervention + physical therapy) or the control group (physical therapy only) with a N of 20 in each group.\n\nThe goal for this research is to determine if dry needling use in the subacute phase of post-operative ACLR following quadriceps autograft can assist with increasing quad strength and improve post-surgical outcomes.",[28,29,30],"Anterior Cruciate Ligament Reconstruction Rehabilitation","Dry Needling","Strength","NOT_YET_RECRUITING","2026-06-15",{"date":34,"type":35},"2026-06-18","ACTUAL",{"date":37,"type":22},"2026-07-01",{"date":39,"type":22},"2027-06-30",{"name":41,"class":42},"Children's Mercy Hospital Kansas City","OTHER",3,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":51,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":23,"phases":56,"briefSummary":57,"conditions":58,"keywords":60,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":79},"100633007","combined-effects-of-stability-oriented-breathing-exercises-and-kegels-exercises-in-postpartum-women-100633007","NCT07521085","Combined Effects Of Stability Oriented Breathing Exercises and Kegel's Exercises in Postpartum Women","Combined Effects Of Stability Oriented Breathing Exercises and Kegel's Exercises On Inter-recti Distance, Lumbopelvic Pain and Strength In Postpartum Women","Inclusion Criteria:\n\n* • Age between 18-40 years\n\n  * Postpartum duration of 42-49 days\n  * Inter-recti distance (IRD) between 3-5 cm\n  * Numeric pain scale score ≤ 6 for pain\n  * No prior physiotherapy or exercise guidance received\n\nExclusion Criteria:\n\n* • Pain during the training period\n\n  * Patients with any heart or respiratory disease including excessive coughing and sneezing\n  * Patients with any kind of pelvic or abdominal surgery\n  * Significant organ dysfunction or psychiatric illness\n  * Diagnosis of malignant tumors","FEMALE","18 Years","40 Years",{"count":55,"type":22},60,[25],"The postpartum period often presents challenges such as increased inter-recti distance (diastasis recti), lumbopelvic pain, and reduced core strength. This study is designed as a randomized controlled trial to evaluate the combined effects of stability-oriented breathing exercises and Kegel exercises on inter-recti distance (IRD), lumbopelvic pain, and muscle strength in postpartum women. A total sample size of 66 participants per group was determined with a 10% dropout rate accounted for.\n\nThe study will use a non-probability convenience sampling technique. It will be conducted at the University of Lahore Teaching Hospital and Sehat Medical complex. Inclusion criteria include women aged 18-40 years, with a history of cesarean sections, an IRD between 3-5 cm. Outcome measures include IRD , pelvic floor muscle strength, lumbopelvic pain (measured using a 10 cm numeric pain scale). Participants will be randomly assigned to either Group A (Kegel-only) or Group B (Kegel + breathing exercises). Both groups will train three times weekly for eight weeks. All data analysis will be performed using SPSS version 27.",[59,30],"Postpartum Complication",[61,62,63,64,65,66,67,68],"Breathing exercises","Core strength","Diastasis recti abdominis","Inter recti distance","Kegel exercises","Lumbopelvic pain","Postpartum women","Stability training","RECRUITING","2026-04-02",{"date":72,"type":35},"2026-04-09",{"date":74,"type":35},"2025-08-31",{"date":76,"type":22},"2026-09",{"name":78,"class":42},"Riphah International University",2,{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":4,"eligibilityCriteria":86,"healthyVolunteers":87,"sex":51,"minAge":52,"maxAge":88,"enrollmentInfo":89,"targetDuration":4,"studyType":91,"phases":4,"briefSummary":92,"conditions":93,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":105,"locationsCount":4},"100623685","investigating-the-effects-of-time-of-day-and-menstrual-cycle-phase-low-and-high-progesterone-on-females-cognitive-and-strength-performance-100623685","NCT07399847","Investigating the Effects of Time-of-day and Menstrual Cycle Phase (Low and High Progesterone) on Female's Cognitive and Strength Performance","Effects of Time-of-day and Menstrual Cycle Phase (Low and High Progesterone) on Female's Cognitive and Strength Performance","Inclusion Criteria:\n\n* Female (assigned at birth)\n* Aged 18-30 years\n* Tier 2 athlete which requires the participants to identify with a specific sport, train with a purpose to compete, regularly train \\~3 times per week and compete at a local level (for example being a member of a BUCS sport and competing regularly with that sport)\n* Regular menstrual cycle - considered between 21-35-day cycles with at least 9 periods a year.\n\nExclusion Criteria:\n\n* The current\u002Fprevious (in the last 3 months) use of any contraceptive method that alter the menstrual cycle\n* The use of the emergency contraceptive pill either 3 months prior to the study or during the study\n* Diagnosis of menstrual disorders including (but not exclusively) endometriosis and Polycystic Ovary Syndrome (PCOS)\n* A formal diagnosis of sleep disorders such as insomnia\n* Consume \\>400mg\u002Fday of caffeine\n* A musculoskeletal injury in the past 3 months\n* A formal diagnosis of neurological or psychiatric disorders such as Attention-Deficit\u002FHyperactivity Disorder (ADHD), Autism Spectrum Disorder (ASD), Dyslexia or schizophrenia\n* Taking prescribed medication that may affect sleep for example stimulants such as Methylphenidate\n* No regular night shift work\n* No trans-meridian travel within 10 days of their expected participation dates (travel that will cause jetlag)\n* Have given blood in the last 12 weeks - this is not strictly an exclusion; participants will just need to wait until after 12 weeks before taking part in the study",true,"30 Years",{"count":90,"type":22},30,"OBSERVATIONAL","This study is designed to determine whether time-of-day and menstrual cycle phase influence athletic performance and is expected to contribute valuable insight into how both time-of-day, and hormonal factors can influence performance and expand existing research. This study aims to support more inclusive, effective and personalised approaches to training and competition schedules for female athletes.\n\nThe study will involve two testing days that require a participant to complete a compilation of tests at 07:00, 12:00 and 18:00 hours. The testing days will be arranged for when a participant is in phase 1 (lowest levels of progesterone in the menstrual cycle) and phase 4 (highest level of progesterone in the menstrual cycle). The tests will examine a participant's executive function and physical strength.\n\nThis study will aim to recruit thirty 18-30-year-old females from Lancaster University who identify with a sport that they train \\~3 times a week for with a purpose to compete. The females recruited must have a regular menstrual cycle and no history of sleep disorders.\n\nAim: To investigate the effects of time-of-day and menstrual cycle phase (low and high progesterone levels) on executive function and strength in females.\n\nObjectives:\n\n1. To determine the effects of time-of-day on executive function and strength tests.\n2. To determine the effects of menstrual cycle phase on executive function and strength tests.\n3. To examine if there is an interaction between time-of-day and menstrual cycle phase on executive function and strength tests.",[94,95,96,97,98,30],"Circadian Rhythm","Menstrual Cycle Phase","Female Athletes","Executive Function (Cognition)","Eumenorrhea","2026-02-05",{"date":101,"type":35},"2026-02-10",{"date":103,"type":22},"2026-02",{"date":76,"type":22},{"name":106,"class":42},"Lancaster University",{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":4,"eligibilityCriteria":113,"healthyVolunteers":11,"sex":17,"minAge":114,"maxAge":4,"enrollmentInfo":115,"targetDuration":4,"studyType":23,"phases":117,"briefSummary":118,"conditions":119,"keywords":125,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":135,"lastUpdatePostDateStruct":136,"startDateStruct":138,"completionDateStruct":140,"leadSponsor":142,"locationsCount":79},"100617748","the-effects-of-medidrink-platinum-and-fava-bean-protein-hydrolysate-on-fitness-in-an-aged-population-100617748","NCT07322653","The Effects of MediDrink Platinum+ and Fava Bean Protein Hydrolysate on Fitness in an Aged Population","Prospective, Open-Label, Multicenter Study to Characterise the Effects of Co-administration of MediDrink Platinum+ Formula Containing Novel Protein Blend SPR-01 and Fava Bean Protein Hydrolysate on Fitness in an Aged Population","Inclusion Criteria:\n\n* 60 years or older\n* BMI ≤ 25 kg\u002Fm²\n* Malnourished (mini nutritional assessment MNA \\\u003C11\n* Sarcopenic: SARC-F score ≥ 4\n* Capable or oral feeding either alone or assisted\n* Ambulatory (WHO PS\u002FECOG 0-3)\n* Ability to complete questionnaires and self assess health status\n* Ability to provide consent\n\nExclusion Criteria:\n\n* Patient cannot eat orally\n* Acute Infection\n* Proven Intestinal obstruction\n* Co-morbidities requiring a special diet (diabetes, kidney disease etc.)\n* Liver dysfunction\n* Acute or chronic renal failure\n* Uncontrollable nausea or vomiting\n* Use of megestrol acetate or metabolic steroids\n* Dietary supplement use in the last 3 months\n* Known intolerance or allergy to the investigational products\n* Participation in any clinical trial within the last 3 months","60 Years",{"count":116,"type":22},75,[25],"Examining the effects of MediDrink Platinum+ containing novel protein blend SRP-01 alone or when combined with PeptiStrong on clinical responses in elderly adults with sarcopenia",[120,121,122,123,124,30],"Sarcopenia in Elderly","Malnourished","Protein Supplementation","Muscle Mass","Physical Function",[126,127,128,129,130,131,132,133,134],"Sarcopenia","Peptide Therapeutics","PeptiStrong","MediDrink Platinum","Malnourished Elderly","Physical functioning","MediDrink Platinum+","Clinical Nurtition","Nutritional status","2025-12-22",{"date":137,"type":35},"2026-01-07",{"date":139,"type":35},"2025-09-10",{"date":141,"type":22},"2027-01-02",{"name":143,"class":144},"Nuritas Ltd","INDUSTRY",{"id":146,"slug":147,"hasResults":11,"nctId":148,"briefTitle":149,"officialTitle":150,"acronym":4,"eligibilityCriteria":151,"healthyVolunteers":87,"sex":51,"minAge":152,"maxAge":153,"enrollmentInfo":154,"targetDuration":4,"studyType":23,"phases":156,"briefSummary":157,"conditions":158,"keywords":162,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":165,"lastUpdatePostDateStruct":166,"startDateStruct":168,"completionDateStruct":170,"leadSponsor":172,"locationsCount":174},"100568979","effects-of-plyometric-exercises-in-female-fast-bowlers-100568979","NCT06688279","Effects of Plyometric Exercises in Female Fast Bowlers","Effects of Plyometric Exercises on Strength, Power and Dynamic Balance in Female Fast Bowlers","Inclusion Criteria:\n\n* Patient between age of 19 to 28 years\n* Female fast bowlers.\n* Active team members of their respective leagues.\n* Healthy, without the presence of injuries.\n* Whose composite score will be greater than 75 on star excursion balance scale.\n\nExclusion Criteria:\n\n* Femles with Injury.\n* History of elbow or shoulder injury or pain within one year of the study's pre-test will be excluded.","19 Years","28 Years",{"count":155,"type":22},28,[25],"Cricket is one of the most popular team sports in the world. Bowling action is an extremely skilled activity that has been developed over many years of practice. Physiological variables and an imbalance between the agonist and antagonist muscle groups are important risk factors for development in high skill bowlers.\n\nExercises known as plyometric training use explosive motions to build muscle mass and improve aspects of physical fitness. Ballistic six plyometric exercises have been shown to improve performance in medium-paced cricket bowlers by increasing bowling velocity.This randomized controlled trial will be conducted in Pakistan Sports Board Lahore. This study will be completed in 10 months after the approval of synopsis. Non-probability convenient sampling technique will be used. Inclusion criteria will include female fast bowlers with age group between19 to 27years who are active team members of their respective leagues without the presence of injuries and whose composite score will be greater than 75 on star excursion balance scale will be included. Any participant post-elbow or shoulder surgery within one year of the study's pre-test or presenting with a history of elbow or shoulder injury or pain within one year of the study's pre-test will be excluded. The study will be conducted in two groups. Group A (14 players) will receive 8 weeks of upper and lower body plyometric exercises protocol. The session will last for 60 minutes and 3 times per week.10-15 mints warm up before plyometric exercises and 1-minute rest period is there between each exercise and each repetition and 3-5 minute for each set. Group B (14 players) will receive their standard exercise protocol. The session will last for 60 minutes and 3 times per week. Vertical jump test for lower extremity strength, 3-Hop test for lower extremity power and Star excursion balance test for dynamic balance is performed at the start of exercise protocol and in the end. After data collection data will be analyzed using statistical package for social sciences SPSS version 21.",[159,30,160,161],"Plyometric Exercises","Dynamic Balance","Power",[159,30,163,164],"dynamic balance","power","2025-01-18",{"date":167,"type":35},"2025-01-22",{"date":169,"type":35},"2024-11-30",{"date":171,"type":22},"2025-05-30",{"name":173,"class":42},"Sehat Medical Complex",1,{"id":176,"slug":177,"hasResults":11,"nctId":178,"briefTitle":179,"officialTitle":180,"acronym":4,"eligibilityCriteria":181,"healthyVolunteers":11,"sex":17,"minAge":182,"maxAge":4,"enrollmentInfo":183,"targetDuration":185,"studyType":91,"phases":4,"briefSummary":186,"conditions":187,"keywords":195,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":199,"lastUpdatePostDateStruct":200,"startDateStruct":202,"completionDateStruct":204,"leadSponsor":206,"locationsCount":174},"100532846","update-on-the-detection-of-frailty-in-older-adults-100532846","NCT06218121","Update on the Detection of Frailty in Older Adults","Update on the Detection of Frailty in Older Adults: A Multicenter Cohort Machine Learning-Based Study","Inclusion Criteria:\n\nA diagnosis of signs and symptoms of frailty by a geriatric physician in the research group will be used as the primary inclusion criterion. Frailty will be assessed and diagnosed using the frailty phenotype and the Clinical Frailty Scale.\n\nExclusion Criteria:\n\n* Acute myocardial infarction in the last 3 months and\u002For unstable angina pectoris\n* Uncontrolled arrhythmia, recent thromboembolism and terminal illness.\n* Patients undergoing MMII unloading or MMSS\u002FMMII fractures in the last three months.\n* Patients with a functional gait index of 1 (Inability to walk)\n* Severe pain (7\u002F10 VAS)\n* Previous neuromuscular pathology presenting with weakness\n* Medication that does not allow the patient's actual muscle reaction to be assessed\n* Severe cognitive impairment that would prevent collaboration and understanding of the tests to be performed.\n* Cardiovascularly unstable patients and uncontrolled arterial hypertension.","62 Years",{"count":184,"type":22},500,"2 Years","The main objective is to update the diagnostic assessment of frailty by correlating several variables with the ultrasound image of the frail elderly patient.\n\nSecondarily, the investigators intend to collect and analyze data on functional capacity and quality of life variables on the evolution of musculoskeletal symptoms, as well as on pain and psychological variables. Similarly, it is intended to make a record of different profiles and subtypes of frail older adult patients to be stored in Machine Learning in order to establish therapeutic intervention plans that allow both the evaluation and treatment of patients.",[30,188,189,190,191,126,192,193,194],"Quality of Life","Functional Independence","Functionality","Pain","Anxiety","Kinesiophobia","Depression",[196,197,126,198],"Frailty","Quality of life","Ultrasound","2024-07-08",{"date":201,"type":35},"2024-07-09",{"date":203,"type":35},"2024-04-20",{"date":205,"type":22},"2025-06-15",{"name":207,"class":42},"Universidad Europea de Madrid"]