[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Universiti Teknologi Mara\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":246},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,53,83,107,136,173,196,221],{"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":31,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100644025","the-simplified-total-body-resistance-exercise-for-muscular-hypertrophy-for-diabetic-population-d-storm-100644025",false,"NCT07664501","The Simplified Total-body Resistance Exercise for Muscular Hypertrophy for Diabetic Population (D-STORM)","The Simplified Total-body Resistance Exercise for Muscular Hypertrophy for Diabetic Population (D-STORM): Rationale and Study Protocol for a Randomized Controlled Trial","D-STORM","Inclusion Criteria:\n\n* Aged 18 to 65 years\n* Confirmed diagnosis of Type 2 Diabetes Mellitus\n* HbA1c between 6.5% and 13.0%\n* Not currently on insulin therapy\n* Has a primary care provider\n\nExclusion Criteria:\n\n* Age below 18 or above 65 years\n* Blood pressure 160\u002F100 mmHg or higher at screening\n* HbA1c below 6.5% or above 13.0%\n* Currently on insulin therapy\n* Pregnant or planning to become pregnant within the next 6 months\n* Serious medical conditions that would prevent safe participation in an exercise programme\n* Any physical or functional limitation that would prevent participation in resistance training\n* Underlying conditions that would not allow safe participation in the exercise intervention","ALL","18 Years","65 Years",{"count":21,"type":22},56,"ESTIMATED","INTERVENTIONAL",[25],"NA","Type 2 diabetes is associated with progressive loss of muscle mass, which worsens blood sugar control and increases the risk of heart disease and disability. Resistance training (weight training) has been shown to build muscle and improve blood sugar levels, but most existing programmes use high intensities that are difficult for older or inactive people with diabetes to sustain.\n\nThis study tests a new resistance training programme called D-STORM (Simplified Total-body Resistance Exercise for Muscular Hypertrophy for Diabetic Population), which uses a lower, more manageable training load designed to be safe, tolerable, and effective for adults with Type 2 diabetes who are not on insulin.\n\nParticipants will be randomly assigned to either twice-weekly D-STORM training plus their usual diabetes care, or usual care alone, for 12 weeks. The main outcome measured is change in HbA1c (a blood test reflecting average blood sugar over 3 months). Body composition, walking capacity, blood pressure, heart rate, and quality of life will also be measured.",[28,29,30],"Type 2 Diabetes Mellitus (T2DM)","Sarcopenia","Insulin Resistance",[32,33,34,35,36,37,38,39],"Type 2 diabetes mellitus","Resistance training","Muscular hypertrophy","Glycaemic control","HbA1c","Cardiometabolic outcomes","Randomised controlled trial","Minimal effective dose","NOT_YET_RECRUITING","2026-06-22",{"date":43,"type":44},"2026-06-25","ACTUAL",{"date":46,"type":22},"2027-01-01",{"date":48,"type":22},"2027-12-31",{"name":50,"class":51},"Universiti Teknologi Mara","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":61,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":62,"targetDuration":4,"studyType":23,"phases":64,"briefSummary":65,"conditions":66,"keywords":68,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":52},"100609308","demensiakita-mobile-health-app-to-improve-knowledge-attitude-practice-and-reduce-burden-among-dementia-caregivers-in-malaysia-100609308","NCT07212894","DemensiaKITA Mobile Health App to Improve Knowledge, Attitude, Practice and Reduce Burden Among Dementia Caregivers in Malaysia","The Effect of DemensiaKITA Mobile Health Application Intervention on Knowledge, Attitude, Practice (KAP) and Burden Level of Dementia Caregivers in Kuala Lumpur and Selangor, Malaysia: Protocol for a Non-Randomized Controlled Trial","DemensiaKITA","Inclusion Criteria:\n\n* Adults aged 18 years and above\n* Primary informal caregiver of a person living with dementia (family member or household member)\n* Able to read and understand Malay\n* Owns a smartphone and is able to use mobile applications\n* Provides informed consent to participate\n\nExclusion Criteria:\n\n* Professional\u002Fpaid caregivers (e.g., nurses, domestic helpers hired solely for caregiving)\n* Caregivers of patients with conditions other than dementia\n* Individuals with severe cognitive or psychiatric illness that limits their ability to participate",true,{"count":63,"type":22},451,[25],"Dementia is a growing health concern in Malaysia and places a heavy burden on family members who act as caregivers. Many caregivers struggle with limited knowledge, negative attitudes, and challenges in daily caregiving practices. These issues increase caregiver stress and reduce the quality of care for people living with dementia.\n\nThe DemensiaKITA mobile health application was developed to support caregivers by providing educational content, self-help tools, and practical guidance. This study will evaluate whether using the DemensiaKITA app can improve caregivers' knowledge, attitudes, and caregiving practices (KAP), as well as reduce caregiver burden.\n\nThis is a non-randomized controlled trial involving dementia caregivers in Kuala Lumpur and Selangor. Participants in the intervention group will use the DemensiaKITA mobile app for a set period, while the control group will continue with usual support. Outcomes will be measured before and after the intervention using validated questionnaires.\n\nThe results of this study will provide evidence on the effectiveness of a locally developed mobile health application in supporting dementia caregivers in Malaysia. If successful, this digital approach may be scaled up to improve caregiver support and dementia care in other settings.",[67],"Dementia",[67,69,70,71,72,73],"Informal Caregivers","Mobile health application","Knowledge Attitude Practice","Burden level","Malaysia","RECRUITING","2025-10-01",{"date":77,"type":44},"2025-10-08",{"date":79,"type":22},"2025-10-10",{"date":81,"type":22},"2026-05-31",{"name":50,"class":51},{"id":84,"slug":85,"hasResults":11,"nctId":86,"briefTitle":87,"officialTitle":88,"acronym":89,"eligibilityCriteria":90,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":91,"targetDuration":4,"studyType":23,"phases":93,"briefSummary":94,"conditions":95,"keywords":97,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":106,"locationsCount":52},"100603245","the-impact-of-perineural-injection-therapy-for-adhesive-capsulitis-100603245","NCT07134010","The Impact of Perineural Injection Therapy for Adhesive Capsulitis.","The Impact of Perineural Injection Therapy for Adhesive Capsulitis at a Single Centre University Hospital in Selangor: A Pilot Study","PIT; AC","Inclusion Criteria:\n\n1. Age 18 and above.\n2. Diagnosed with primary adhesive capsulitis by a specialist.\n3. Limitation of range of motion ≥ 50% relative to the normal side or normal reference (in patient with bilateral adhesive capsulitis) in three or more movement directions (i.e., external rotation, abduction, forward flexion, and internal rotation).\n4. Chronic adhesive capsulitis shoulder pain lasting for at least 3 months.\n5. Pain score of at least 4\u002F10 on the Numerical Rating Scale (NRS) during movement, indicating at least moderate pain severity.\n6. Consented to the study.\n\nExclusion Criteria:\n\n1. Received any shoulder pain injection within the past 6 weeks or surgical intervention such manipulation under anesthesia, arthroscopic capsular release, or open surgery for capsular release.\n2. Diagnosed with other shoulder pathology such as neurologic deficits affecting shoulder function, tumour, rotator cuff injury or fracture.\n3. Has history of allergy to dextrose solution.\n4. Patients receiving steroidsimmunosuppressants, psychotropic medication, or other medications that may affect, the clinical outcomes\n5. Patients with haemorrhagic disease, taking anticoagulant drugs, or patients with severe diabetes mellitus having an increased risk of infection (HBA1c \\>8%)\n6. Do not understand Malay or English language.\n7. Unable to follow a 3 steps command.",{"count":92,"type":22},24,[25],"The goal of this clinical trial is to learn if Perineural Injection Therapy (PIT) works to treat adhesive capsulitis (frozen shoulder) in adults. It will also learn about the safety of PIT.\n\nThe main questions it aims to answer are:\n\nDoes PIT reduce shoulder pain and improve shoulder range of motion more effectively than conventional therapy alone?\n\nWhat side effects or medical problems do participants experience when receiving PIT?\n\nResearchers will compare PIT to conventional therapy to see if PIT works better to treat adhesive capsulitis.\n\nParticipants will:\n\nReceive either:\n\nPIT once weekly for 6 weeks plus physiotherapy and oral analgesics (excluding NSAIDs), or\n\nConventional therapy only (physiotherapy and analgesics including NSAIDs)\n\nAttend scheduled follow-up visits at Week 6, 1 month, and 3 months after treatment\n\nPerform daily home-based shoulder exercises and record their analgesic use and any side effects in a patient diary",[96],"Adhesive Capsulitis",[98],"Perineural injection therapy in treating Adhesive Capsulitis","2025-08-27",{"date":101,"type":44},"2025-09-04",{"date":103,"type":44},"2025-06-03",{"date":105,"type":22},"2026-06-01",{"name":50,"class":51},{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":113,"eligibilityCriteria":114,"healthyVolunteers":61,"sex":17,"minAge":115,"maxAge":116,"enrollmentInfo":117,"targetDuration":4,"studyType":23,"phases":119,"briefSummary":120,"conditions":121,"keywords":124,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":128,"lastUpdatePostDateStruct":129,"startDateStruct":131,"completionDateStruct":133,"leadSponsor":135,"locationsCount":4},"100592428","arpe-training-for-manual-handling-workers-a-quasi-experimental-study-on-ergonomic-knowledge-and-practice-100592428","NCT06993298","ARPE Training for Manual Handling Workers: A Quasi-Experimental Study on Ergonomic Knowledge and Practice","Development and Effectiveness of the Augmented Reality Physical Ergonomics (ARPE) Training Module for Manual Material Handling Workers: A Quasi-Experimental Study Protocol","ARPE;MMH","Inclusion Criteria:\n\nMalaysian citizen\n\nAge 18 years and above\n\nCurrently employed as a manual material handling (MMH) worker in a warehouse\n\nRegularly performs MMH tasks (e.g., lifting, lowering, pushing, pulling, carrying, holding, or restraining objects weighing 14 kg or more)\n\nWorks a minimum of 8 hours per day in a role involving MMH\n\nOwns a mobile phone capable of downloading and running the MAKAR XR app\n\nExclusion Criteria:\n\nPregnant\n\nCurrently an intern or temporary worker\n\nHas undergone ergonomic training within the past six months","20 Years","60 Years",{"count":118,"type":22},78,[25],"The goal of this study is to evaluate whether an Augmented Reality-based ergonomic training module (ARPE) can improve ergonomic knowledge, self-prevention, and self-evaluation practices among adult manual material handling (MMH) workers in warehouses. The main questions it aims to answer are:\n\nDoes the ARPE training module improve workers' ergonomic knowledge?\n\nDoes it enhance their ability to prevent and assess risks of work-related musculoskeletal disorders (WMSDs)?\n\nResearchers will compare an intervention group using the ARPE module with a control group receiving traditional training based on national ergonomic guidelines to see if the AR module leads to better outcomes.\n\nParticipants will:\n\nAttend a briefing and use the ARPE training via the MAKAR XR app\n\nComplete self-assessment questionnaires at baseline, week 1, and week 6\n\nReceive reminders and follow-ups through WhatsApp",[122,123],"Occupational Diseases","Work Related Upper Limb Disorder",[125,126,127],"Augmented Reality (AR)","Ergonomic","Work Related Musculo skeletal Disorder (WMSD)","2025-05-23",{"date":130,"type":44},"2025-05-28",{"date":132,"type":22},"2025-09-01",{"date":134,"type":22},"2026-10-01",{"name":50,"class":51},{"id":137,"slug":138,"hasResults":11,"nctId":139,"briefTitle":140,"officialTitle":141,"acronym":4,"eligibilityCriteria":142,"healthyVolunteers":61,"sex":17,"minAge":18,"maxAge":143,"enrollmentInfo":144,"targetDuration":4,"studyType":23,"phases":146,"briefSummary":147,"conditions":148,"keywords":158,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":164,"lastUpdatePostDateStruct":165,"startDateStruct":167,"completionDateStruct":169,"leadSponsor":171,"locationsCount":172},"100557571","creating-a-new-health-promotion-module-to-help-the-indigenous-people-of-selangor-prepare-for-disease-x-and-outbreaks-100557571","NCT06539845","Creating a New Health Promotion Module to Help the Indigenous People of Selangor Prepare for Disease X and Outbreaks","Development and Effectiveness of a New Intervention on Household Preparedness for Disease X and Outbreaks Among Orang Asli in Selangor: A Cluster Randomized Trial","Inclusion Criteria:\n\n* Orang Asli ethnicity\n* Malaysian citizen\n* Age between 18 to 99 years old\n* The head of the household, or the person who contributes to, or influences health-related decisions for the household\n* Live in a household with at least three members\n* Able to converse in Malay\n\nExclusion Criteria:\n\n* Having physical or cognitive disabilities (e.g., blindness, deafness, schizophrenia and dementia)\n* Having severe health conditions (e.g., respiratory and cardiovascular disease requiring oxygen support such as severe asthma\u002Fchronic obstructive pulmonary disease\u002Fheart failure and congenital heart diseases)\n* Residing temporarily (less than 2 years)\n* Intending to relocate to a different residence within the next 2 years","99 Years",{"count":145,"type":22},96,[25],"The goal of this cluster randomized trial is to develop and test a new method for preparing indigenous (locally termed as Orang Asli) households in Selangor, a state in Malaysia, for outbreaks and Disease X, a potential unknown infectious threat. It aims to determine if the new method, a health education package comprised of workshops, simulation exercises, and card game play sessions, can enhance the readiness of these families for such outbreaks.\n\nThe main questions it is looking to answer are:\n\n1. Will the intervention package increase the level of preparedness for a Disease X and outbreaks among indigenous households in Selangor?\n2. Will the intervention improve the awareness and attitudes of the indigenous people in Selangor towards outbreak preparedness?\n3. Will it lead to more proactive preparedness actions by these households?\n\nTo evaluate the effectiveness of the intervention package, researchers will compare outcomes between two groups: the intervention group receiving both the intervention package and educational brochures on communicable disease prevention, and the control group receiving only the brochures.\n\nParticipants will:\n\n1. Participate in the activities in the newly developed intervention package, which would include workshops, simulation exercises, and card game play sessions.\n2. Answer surveys four times: before, immediately after, 1 month after and 2 months after the intervention, to measure any changes in their preparedness levels for an outbreak.",[149,150,151,152,153,154,155,156,157],"Attitude to Health","Behavior, Health","Health Behavior","Health-Related Behavior","Health Attitude","Health Knowledge, Attitudes, Practice","Knowledge, Attitudes, Practice","Preparedness","Outbreaks",[159,160,156,161,162,163],"Indigenous People","Aboriginal","Readiness","Community Trial","Outbreak","2025-04-12",{"date":166,"type":44},"2025-04-16",{"date":168,"type":22},"2025-06",{"date":170,"type":22},"2025-09",{"name":50,"class":51},2,{"id":174,"slug":175,"hasResults":11,"nctId":176,"briefTitle":177,"officialTitle":178,"acronym":4,"eligibilityCriteria":179,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":116,"enrollmentInfo":180,"targetDuration":4,"studyType":23,"phases":182,"briefSummary":183,"conditions":184,"keywords":186,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":188,"lastUpdatePostDateStruct":189,"startDateStruct":191,"completionDateStruct":193,"leadSponsor":195,"locationsCount":4},"100562167","impact-of-combined-cst-bfr-and-tai-chi-on-muscle-physiology-and-functional-characteristics-among-adults-with-lbp-100562167","NCT06599645","Impact of Combined CST, BFR, and Tai Chi on Muscle Physiology and Functional Characteristics Among Adults With LBP","Impact of Combined Core Stability Training, Blood Flow Restriction, and Tai Chi on Muscle Physiology and Functional Characteristics Among Adults With Low Back Pain","Inclusion Criteria:\n\n* All participants had stable vital signs, were cognizant, and had no cognitive impairment.\n* Aged 18-60 years old, able to understand Mandarin Chinese, and willing to cooperate.\n* LBP duration ≥ 3 months.\n* Be diagnosed as NLBP.\n* VAS score ≤ 5 points.\n\nExclusion Criteria:\n\n* Patients with severe heart disease, liver disease, renal disease, pulmonary insufficiency, tumors, and postoperative dysfunction.\n* Patients who are unconscious and unable to cooperate.\n* Spinal fractures, severe arthritis, bony spinal stenosis, ankylosing spondylitis, open fractures, or unhealed traumatic wounds.\n* Patients who have not been diagnosed with NLBP.\n* Unable to communicate and read in Chinese.\n* Age \\\u003C18 \\& \\>60 years old.\n* LBP duration \\\u003C 3 months.\n* Patients with high blood pressure and abnormal heartbeat.\n* VAS score \\> 5 points.",{"count":181,"type":22},52,[25],"Background:\n\nLow back pain (LBP) is highly prevalent globally, affecting people of all ages(Wu et al., 2020). In China, LBP is a leading cause of disease burden(Wu et al., 2019). Exercise therapy such as core stability training(CST), Tai Chi(TC) and education are commonly recommended treatments, but research on optimal protocols has been limited. Blood flow restriction(BFR) is beneficial for inducing muscle hypertrophy and promoting muscle strength (Hughes et al., 2019). Combined approaches using multiple modalities may provide added benefits but are understudied.\n\nResearch objectives:\n\n1. To determine the effects of combined CST, BFR and Tai Chi on muscle physiology (muscle activation, muscle fatigue, back extensor strength, and transverses abdominus control) among working adults with LBP.\n2. To determine the effects of combined CST+ BFR+Tai Chi on functional performance (gait speed, balance, proprioception, and postural sway) among working adults with LBP.\n3. To determine the effects of combined CST+BFR+Tai Chi on pain intensity among working adults with LBP.\n4. To determine the effects of combined CST+BFR+Tai Chi on fear among working adults with LBP.\n\nLocation of research:\n\nQianxinan Wutong Orthopedic Hospital, Guizhou Province, China\n\nInstrumentations:\n\n1. Demographic Data\n2. Surface Electromyography (S-EMG)\n3. Pressure Biofeedback Unit (PBU)\n4. Back Extensor Strength Test (BEST)\n5. Joint Repositioning Error(JRE)\n6. APECS app\n7. Y-Balance Test(YBT)\n\n8.10-Meter Walk Test(10MWT)\n\n9.Visual Analogue Scale (VAS)\n\n10.Chinese version of the Fear-Avoidance Beliefs Questionnaire(FABQ-CHI)\n\nInterventions:\n\nGroup A: CST+BFR+Tai Chi+Education;\n\nGroup B: CST+BFR+Education;\n\nGroup C: Tai Chi +BFR+Education;\n\nGroup D: CST+Education.\n\nSample size:\n\nConsidering 30% drop out. 52 participants. 13 participants in each group\n\nStatistical analysis:\n\nData were processed using SPSS version 25.0 and Microsoft Excel 2010 software.\n\n1. Demographic data = descriptive analytics.\n2. All objectives = repeated measure ANCOVA (within-between interactions) for all variables.\n3. The significant level is P \\\u003C 0.05.",[185],"Low Back Pain",[187],"Tai Ji; Core stability; Low back pain","2024-09-13",{"date":190,"type":44},"2024-09-19",{"date":192,"type":22},"2024-10-08",{"date":194,"type":22},"2025-07-31",{"name":50,"class":51},{"id":197,"slug":198,"hasResults":11,"nctId":199,"briefTitle":200,"officialTitle":200,"acronym":4,"eligibilityCriteria":201,"healthyVolunteers":61,"sex":17,"minAge":202,"maxAge":203,"enrollmentInfo":204,"targetDuration":4,"studyType":23,"phases":206,"briefSummary":207,"conditions":208,"keywords":209,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":213,"lastUpdatePostDateStruct":214,"startDateStruct":216,"completionDateStruct":218,"leadSponsor":220,"locationsCount":172},"100557828","effectiveness-of-metaverse-based-immersive-technology-intervention-for-oral-health-education-a-quasi-experimental-study-100557828","NCT06543186","Effectiveness of Metaverse-Based Immersive Technology Intervention for Oral Health Education: A Quasi-Experimental Study","Inclusion Criteria:\n\n1. aged 15-16 years old in 2024\n2. voluntarily wish to participate in the research with consent from their legal guardians\n3. enrolled in a co-education school (providing education to both boys and girls)\n4. willing to commit to the program\n5. can understand both Malay and English\n6. participating schools must possess the necessary computer facilities to facilitate this aspect of the study\n\nExclusion Criteria:\n\n1. aged less or more than 15-16 years old in 2024\n2. not voluntarily wish to participate in the research with consent from their legal guardians\n3. not enrolled in a co-education school (providing education to both boys and girls)\n4. not willing to commit to the program\n5. can't understand both Malay and English\n6. participating schools does not possess the necessary computer facilities to facilitate this aspect of the study","15 Years","16 Years",{"count":205,"type":22},210,[25],"To evaluate the effectiveness of pre- and post-intervention of oral health education using three interventions (conventional methods, mHealth, and the Metaverse platform) on the oral health status, knowledge, practices, and attitudes among secondary school students in Malaysia.",[155],[210,211,212],"metaverse","immersive technology","virtual reality","2024-08-03",{"date":215,"type":44},"2024-08-07",{"date":217,"type":22},"2024-08-01",{"date":219,"type":22},"2025-05-31",{"name":50,"class":51},{"id":222,"slug":223,"hasResults":11,"nctId":224,"briefTitle":225,"officialTitle":226,"acronym":227,"eligibilityCriteria":228,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":229,"targetDuration":4,"studyType":23,"phases":231,"briefSummary":232,"conditions":233,"keywords":235,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":239,"lastUpdatePostDateStruct":240,"startDateStruct":242,"completionDateStruct":244,"leadSponsor":245,"locationsCount":52},"100516701","time-restricted-eating-study-tres-impacts-on-anthropometric-cardiometabolic-and-cardiovascular-health-100516701","NCT06007950","Time-restricted Eating Study (TRES): Impacts on Anthropometric, Cardiometabolic and Cardiovascular Health","Impacts of Time-Restricted Eating on Weight, Cardiometabolic and Cardiovascular Health in Patients With Acute Coronary Syndrome","TRES","Inclusion Criteria:\n\n* Adult, 18- 65 years old.\n* Had history of acute coronary syndrome (ACS)\n* Clinically stable\n* Self-reported eating window of at least 12 h per day.\n\nExclusion Criteria:\n\n* Severe obesity (body mass index ≥40 kg m-2).\n* Unstable weight in the past three months (gain or lose more than 4 kg of weight).\n* Unstable cardiovascular, renal, cardiac, liver, lung, adrenal, or nervous system disease that may compromise study validity.\n* Any medications or supplements known to change sleep, circadian rhythms, or metabolism.\n* Pregnant or lactating women.\n* Perform overnight shift work more than one day\u002Fweek on average.\n* Regularly fasted for more than 15 hours\u002Fday or having completed twelve 24-hr fasts within the past three months).\n* Active use of tobacco or illicit drug or history of treatment for alcohol abuse.\n* Type I diabetes or diabetic, treated with insulin.\n* Use of anti-obesity drugs or other drugs affecting body weight.\n* Currently enrolled in weight loss or management programme, including surgical intervention.\n* Severe kidney failure (glomerular filtration rate (GFR) \\\u003C30 mL\u002Fmin).\n* Eating disorder or current diagnosis of uncontrolled psychiatric illness, which may impair study involvement.\n* Malignancy undergoing active treatment.\n* Had gastrointestinal surgery or impaired nutrient absorption.\n* Travelled more than two time zones away two months prior to enrolling in the trial or will travel more than two time zones away during the study period.\n* Concurrent participation in other interventional studies",{"count":230,"type":22},48,[25],"The goal of this clinical trial is to learn about the effects of time-restricted eating in patients with history of acute coronary syndrome. The main questions it aims to answer are: 1) Is 10-hr TRE safe and feasible for patients with ACS; 2)What are the impacts of 10-hr TRE on anthropometric measurements, cardiometabolic health and cardiovascular health compared to ad libitum eating in patients with ACS?. Participants will be asked to limit eating duration to 10 hours daily.",[234],"Myocardial Infarction",[236,237,238],"coronary heart disease","time-restricted eating","intermittent fasting","2024-07-17",{"date":241,"type":44},"2024-07-18",{"date":243,"type":44},"2023-09-01",{"date":170,"type":22},{"name":50,"class":51},""]