[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Nanyang Technological University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":325},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,11,0,[8,46,80,110,134,163,188,215,239,270,304],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100601911","feasibility-study-of-single-session-solution-focused-consultation-to-enhance-treatment-engagement-100601911",false,"NCT07116655","Feasibility Study of Single-session Solution Focused Consultation to Enhance Treatment Engagement","Improving Mental Health Treatment Engagement of Patients With Comorbid Chronic Diseases: A Randomized Controlled Evaluation of the Feasibility and Preliminary Effectiveness of a Single-Session Solution-Focused Consultation (SSC) in a Community Setting","Inclusion Criteria: 1. A history of one or more chronic physical diseases based on the Ministry of Health (Singapore) Chronic Disease Management Programme guidelines; 2. A score of 5 or more on the Patient Health Questionnaire (PHQ-9) or Generalized Anxiety Disorder-7 (GAD-7); 3. Not currently engaged in formal mental health service; 4. Conversant in the English language; 5. Receiving treatment in a community healthcare setting\n\nExclusion Criteria: 1. A history of psychosis, intellectual disability, or pervasive developmental disorders","ALL","21 Years","99 Years",{"count":20,"type":21},60,"ESTIMATED","INTERVENTIONAL",[24],"NA","This research aims to explore whether a single-session solution-focused consultation (SSC) can increase mental health service engagement among patients with comorbid chronic physical diseases and mental health problems (CPDMHP).",[27],"Treatment Engagement",[29,30,31,32],"treatment engagement","chronic physical health problems","comorbid mental health problems","single-session intervention","RECRUITING","2026-06-24",{"date":36,"type":37},"2026-06-26","ACTUAL",{"date":39,"type":37},"2025-02-26",{"date":41,"type":21},"2026-12",{"name":43,"class":44},"Nanyang Technological University","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":54,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":62,"conditions":63,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":45},"100631210","phase-2-virtual-menstrual-pain-approaches-in-females-100631210","NCT07497711","Virtual Menstrual Pain Approaches in Females","Virtual Auricular Acupressure and Baduanjin Qigong Exercise for Preventing Menstrual Pain in Females: A Randomized Clinical Trial","AABQ","Inclusion Criteria:\n\n* 16 - 35 years of age\n* Regular menstrual cycles (28 days ± 7 days) in 3 months prior to enrollment\n* Two or more episodes of menstrual cramps in the past 2 months, scored at least 4 points on the worst pain item of the Brief Pain Inventory (BPI)\n* Stated willingness to comply with all study procedures and availability for the duration of the study\n* Ability to download, install, and navigate the study-specific digital content and use its core functions for training, self-guided intervention administration, and data entry\n* Ability to understand the nature of the study and willingness to give informed consent.\n\nExclusion Criteria:\n\n* Uncontrolled neurological diseases, immunodeficiency, bleeding disorders, and allergies\n* The presence of another Axis I disorder not in remission\n* Lactating or pregnant, or those planning to become pregnant in the coming half year\n* Undergoing other trials for pain management during the study period\n* Plan to initiate other pain therapies for menstrual pain management in the proceeding 3 months","FEMALE","16 Years","35 Years",{"count":58,"type":21},145,[60,61],"PHASE2","PHASE3","This research study is testing two self-care approaches that may help prevent or reduce period pain in young females with recurrent painful menstrual cramps. Participants will be placed by chance into 1 of 3 groups: auricular acupressure, Baduanjin qigong, or a self-care education comparison group. The auricular acupressure and Baduanjin groups will receive online training and then practice the treatment on their own for 12 weeks. The main question is whether these two approaches can reduce the severity of menstrual pain. The study will also look at whether they can improve other symptoms that often happen with period pain, such as tiredness, poor sleep, anxiety, low mood, trouble concentrating, and reduced physical function. Researchers will also study stool and blood-related biological markers to better understand whether changes in gut bacteria and body metabolism may be linked to symptom improvement. A total of 145 participants will take part in the study at NTU, and any side effects or other safety concerns will be checked every week.",[64,65,66,67,68,69,70,71],"Pain (Visceral, Somatic, or Neuropathic)","Women of Reproductive Age","Mental Disorder","Digital Health","Acupressure","Traditional Exercise","Host-Gut Microbiota Interaction","Metabolomics","2026-06-18",{"date":74,"type":37},"2026-06-23",{"date":76,"type":37},"2026-04-15",{"date":78,"type":21},"2029-03-20",{"name":43,"class":44},{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":84,"acronym":4,"eligibilityCriteria":85,"healthyVolunteers":86,"sex":16,"minAge":87,"maxAge":88,"enrollmentInfo":89,"targetDuration":4,"studyType":22,"phases":91,"briefSummary":92,"conditions":93,"keywords":95,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":102,"lastUpdatePostDateStruct":103,"startDateStruct":105,"completionDateStruct":107,"leadSponsor":109,"locationsCount":45},"100635712","investigating-cognitive-flexibility-training-100635712","NCT07556250","Investigating Cognitive Flexibility Training","Inclusion Criteria:\n\n* Healthy volunteer (male of female) between 18 and 29 years who gave written informed consent to participate\n\nExclusion Criteria:\n\n* Current and\u002For prior history of learning disabilities\n* Current and\u002For prior history of neurological disorder\n* Current and\u002For prior history of psychiatric disorder\n* Current and\u002For prior history of cardiovascular disorder\n* Predominantly left-handed\n* Contraindications for MRI (e.g., pacemakers, implanted pumps, metal objects in the body)\n* Claustrophobic\n* Pregnancy (females)\n* Lactation (females)\n* Pronounced visual or auditory impairments",true,"18 Years","29 Years",{"count":90,"type":21},225,[24],"The investigators' previous research identified two distinct subtypes of Cognitive Flexibility (CF), termed CF1 (shifting flexibility) and CF2 (strategy flexibility). The present study aims to determine whether these forms of CF can be trained, how they differ, and the extent to which improvements transfer to broader learning and cognitive skills. In addition, social functioning outcomes and the extent to which social factors moderate the effects of cognitive flexibility training are assessed. The investigators will employ a multi-modal approach combining cognitive-behavioural and neuroimaging methods to examine how brain mechanisms and cognitive performance change following CF-targeted training intervention (Structure learning) compared with active control and a no-training paradigm (passive control).",[94],"Healthy",[96,97,98,99,100],"Structure Learning","Cognitive Flexibility","Neural Activation","Intervention","Predictive statistics","NOT_YET_RECRUITING","2026-04-22",{"date":104,"type":37},"2026-04-29",{"date":106,"type":21},"2026-04-23",{"date":108,"type":21},"2026-12-31",{"name":43,"class":44},{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":114,"acronym":115,"eligibilityCriteria":116,"healthyVolunteers":86,"sex":16,"minAge":117,"maxAge":118,"enrollmentInfo":119,"targetDuration":4,"studyType":22,"phases":121,"briefSummary":122,"conditions":123,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":127,"lastUpdatePostDateStruct":128,"startDateStruct":129,"completionDateStruct":131,"leadSponsor":133,"locationsCount":45},"100625693","building-cognitive-behavioural-skills-with-storybooks-to-reduce-emotional-difficulties-in-kindergarten-years-100625693","NCT07425951","Building Cognitive Behavioural Skills With StoryBooks to Reduce Emotional Difficulties in Kindergarten Years","B-READY","Inclusion Criteria:\n\n* Currently be enrolled in K1 or K2 in preschool.\n* Singaporean Citizen or of Permanent Resident status\n* Parent of study's participant has to have read a book with participant at least once in the last 6 months.\n\nExclusion Criteria:\n\n* Not currently enrolled in a child support programme\n* Not currently receiving medication for mental health concerns\n* Not currently receiving support from a Speech Language Therapist or Psychologist.","4 Years","6 Years",{"count":120,"type":21},56,[24],"This research aims to ask (1) Are child and parent measures of coping skills, anxiety and other outcomes reliable (2) How feasible and acceptable is the proposed CB preventative program and protocol (3) Can a preliminary indication of efficacy for CB preventative program be provided.",[124,125,126],"Anxiety","Coping Skills","Socio-emotional Well-being","2026-04-12",{"date":76,"type":37},{"date":130,"type":37},"2026-03-23",{"date":132,"type":21},"2026-11-30",{"name":43,"class":44},{"id":135,"slug":136,"hasResults":11,"nctId":137,"briefTitle":138,"officialTitle":138,"acronym":4,"eligibilityCriteria":139,"healthyVolunteers":86,"sex":16,"minAge":87,"maxAge":140,"enrollmentInfo":141,"targetDuration":4,"studyType":22,"phases":143,"briefSummary":144,"conditions":145,"keywords":149,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":155,"lastUpdatePostDateStruct":156,"startDateStruct":158,"completionDateStruct":160,"leadSponsor":162,"locationsCount":45},"100615152","effects-of-pulsed-electromagnetic-field-therapy-on-sport-performance-and-recovery-100615152","NCT07288892","Effects of Pulsed Electromagnetic Field Therapy on Sport Performance and Recovery","Inclusion Criteria:\n\n* Exercise at least twice a week in the past 3 months\n* Perform resistance training 1-3 times per week in the past 3 months.\n* Have competed in at least two matches \u002F events in the past one year (e.g. heat and final are counted as two events).\n\nExclusion Criteria:\n\n* History of fracture or surgery over the past year.\n* History of musculoskeletal injury in the last 3 months that required more than 7 days of rest.\n* Currently experiencing any injury, discomfort and\u002For pain at the time of study.","30 Years",{"count":142,"type":21},30,[24],"The goal of this clinical trial is to learn if pulsed electromagnetic field (PEMF) therapy works to improve sports performance and recovery in athletes. The main questions it aims to answer are:\n\n* Does PEMF therapy enhance participants' performance during exercise?\n* Does PEMF therapy enhance recovery in participants after exercise? Researchers will compare active PEMF therapy to sham PEMF therapy (using the same device for both, but without any electromagnetic fields) to see if active PEMF therapy is effective in improving sports performance and recovery.\n\nParticipants will:\n\n* Receive active pulsed electromagnetic field therapy or sham pulsed electromagnetic field therapy twice a week for 8 weeks.\n* Visit the laboratory at baseline, 8 weeks, and 12 weeks for sports performance and recovery assessments.",[146,147,148],"Sport Performance","Sport Recovery","Athlete",[150,151,152,153,154],"PEMF","Sport","Performance","Recovery","Exercise","2026-04-06",{"date":157,"type":37},"2026-04-08",{"date":159,"type":37},"2026-01-19",{"date":161,"type":21},"2026-08-30",{"name":43,"class":44},{"id":164,"slug":165,"hasResults":11,"nctId":166,"briefTitle":167,"officialTitle":168,"acronym":4,"eligibilityCriteria":169,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":170,"enrollmentInfo":171,"targetDuration":4,"studyType":22,"phases":172,"briefSummary":173,"conditions":174,"keywords":177,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":155,"lastUpdatePostDateStruct":181,"startDateStruct":183,"completionDateStruct":185,"leadSponsor":187,"locationsCount":45},"100562902","electro-acupuncture-for-obese-patients-with-insulin-resistance-100562902","NCT06609200","Electro-Acupuncture for Obese Patients With Insulin Resistance","Electro-acupuncture for the Obese Patient With Insulin Resistance: a Randomized Sham-controlled Clinical Trial","Inclusion Criteria:\n\n* Men and women aged between 21 and 65 years old\n* BMI ≥ 25 kg\u002Fm2\n* HOMA-IR ≥ 2.14, (HOMA-IR = fasting insulin (ųU\u002FmL)\\* fasting glucose (mmol\u002FL)\u002F22.5)\n* Not receiving any other weight control measures or any medical and\u002For drug history in the last 3 months\n\nExclusion Criteria:\n\n* Diabetes mellitus\n* Treating with drugs that may affect insulin sensitivity\n* Changes 10% of usual body weight in the previous 6 months weight\n* Endocrine diseases, including thyroid disorder, pituitary disorder, sex gland disorder, etc.\n* Heart diseases, including arrhythmia, heart failure, and myocardial infarction, participants with pacemakers\n* Allergy and immunology diseases\n* Bleeding tendency\n* Pregnant or lactating women\n* Impaired hepatic or renal function\n* Stroke or unable to exercise","65 Years",{"count":20,"type":21},[24],"This clinical trial aims to evaluate the efficacy and safety of electro-acupuncture for obese patients with insulin resistance. 60 participants will be randomized and allocated to either the electro-acupuncture arm or the sham acupuncture arm.",[175,176],"Obesity","Insulin Resistance",[178,179,180],"electroacupuncture","obesity","insulin resistance",{"date":182,"type":37},"2026-04-09",{"date":184,"type":37},"2024-10-10",{"date":186,"type":21},"2026-10-09",{"name":43,"class":44},{"id":189,"slug":190,"hasResults":11,"nctId":191,"briefTitle":192,"officialTitle":193,"acronym":194,"eligibilityCriteria":195,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":196,"targetDuration":4,"studyType":22,"phases":198,"briefSummary":199,"conditions":200,"keywords":202,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":207,"lastUpdatePostDateStruct":208,"startDateStruct":210,"completionDateStruct":212,"leadSponsor":214,"locationsCount":45},"100628544","peer-enriched-environment-for-recovery-peer-100628544","NCT07463014","Peer Enriched Environment for Recovery (PEER)","Peer Enriched Environment for Recovery (PEER): An Integrated Health Coaching Intervention Post-Stroke","PEER","Inclusion criteria for peer coach:\n\n* Aged 21 years and above\n* Diagnosed with stroke within the past 5 years and discharged from the hospital\n\nInclusion criteria for intervention recipients\n\n* Aged 21 years and above\n* Diagnosed with stroke within the past 1 year and discharged from the hospital\n\nExclusion criteria for all participants:\n\n* Unable to communicate in English\n* Unable to provide informed consent\n* Diagnosed with one or multiple conditions which affect cognitive and\u002For mental health severely\n* Diagnosed with severe or potentially terminal co-morbidities",{"count":197,"type":21},20,[24],"The goal of this interventional study is to assess whether a peer coaching intervention (PEER) can improve the well-being in individuals who experienced a stroke. The main questions it aims to answer are\n\n1. Is the PEER intervention feasible and acceptable for the intervention recipients who receive the intervention?\n2. Is the PEER intervention feasible and acceptable for the peer coaches who deliver the intervention?\n3. Do intervention recipients show a higher level of quality of life at immediate, 4-week, and 8-week post-intervention?\n4. Do intervention recipients display increases in measures of psycho-social-spiritual well-being at immediate, 4-week, and 8-week post-intervention? Peer coach participants will a) take training sessions, b) deliver 5 coaching sessions to an intervention recipient participant, c) complete surveys before training, after training, and after intervention delivery, and d) participate in a personal interview Intervention recipient participants will a) attend 5 coaching sessions delivered by a peer coach participant, b) complete surveys before intervention, immediately post intervention, 4-week post intervention, and 8 week post-intervention, and c) participate in a personal interview.",[201],"Stroke",[203,204,205,206],"peer coaching","peer support","post-stroke care","rehabilitation","2026-03-06",{"date":209,"type":37},"2026-03-10",{"date":211,"type":37},"2025-01-01",{"date":213,"type":21},"2026-08",{"name":43,"class":44},{"id":216,"slug":217,"hasResults":11,"nctId":218,"briefTitle":219,"officialTitle":219,"acronym":220,"eligibilityCriteria":221,"healthyVolunteers":86,"sex":16,"minAge":222,"maxAge":18,"enrollmentInfo":223,"targetDuration":4,"studyType":22,"phases":225,"briefSummary":226,"conditions":227,"keywords":229,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":232,"lastUpdatePostDateStruct":233,"startDateStruct":235,"completionDateStruct":237,"leadSponsor":238,"locationsCount":45},"100572363","stronger-families-through-art-therapy-a-mixed-methods-programme-evaluation-study-100572363","NCT06732297","Stronger Families Through Art Therapy: A Mixed Methods Programme Evaluation Study","SFAT","Inclusion Criteria (family participant):\n\n* the caregiver (including parents, grandparents, family members or foster parents who perform the main caretaking responsibilities of the children taking part in SFAT) of a young child who can communicate in English and provide informed consent\n* the child is aged 7-14 years and can communicate in English\n* the family have one or more of the following identified challenges: (1) caregiver stress such as finances, household management, work and childcare arrangements, (2) caregiver struggles to find time for self-care and quality time with children, (3) caregiver has minimal understanding of the psychological and emotional needs of their children, (4) children face difficulties with emotional regulation and anger management\n* caregivers and children are from low-income families who receive financial assistance under the CHAS Blue card, ComCare financial assistance, and\u002For the MOE Financial Assistance Scheme\n\nInclusion criteria (art therapist participant) registered art therapist based in the Red Pencil (Singapore) who are in charge of delivering the SFAT programme\n\nInclusion criteria (community staff participant)\n\n\\- community staff who provides assistance to the implementation of the SFAT programme\n\nExclusion Criteria:\n\n* individuals who are suffering from depression or other major mental health conditions that would render their participation highly disruptive to others in a group setting, and\u002For cannot provide informed consent. Families will also be excluded if they are currently unstable (i.e. circumstances related to abuse\u002Fneglect), and\u002For have high risk of suicidal and self-harm behaviours. In the cases that individuals referred to the programme are not eligible, the partner organisations will assess their needs and refer them to programmes based on these needs.\n* participant is unable to provide informed consent","7 Years",{"count":224,"type":21},96,[24],"The current research aims to evaluate the effectiveness and feasibility of the Strong Families Through Art Therapy (SFAT) programme, which was developed to improve the parent-child relationship in vulnerable families. The main questions it aims to answer are:\n\n1. Is the programme effective in enhancing quality of life and family resilience among parents?\n2. Is the programme effective in enhancing quality of life among children?\n3. Is the programme feasible and acceptable for large scale implementation in Singapore?\n\nResearchers will compare the status of family participants (caregivers and children) before and after they take the programme and compare family participants who take the programme with family participants who have not yet taken the programme to see if the programme is effective in benefiting the participants. Researchers will also invite family participants to discuss about the programme.\n\nFamily participants will\n\n1. Take the 10-week SFAT programme\n2. Complete assessment survey for 3 times\n3. Attend a focus group discussion (optional)\n\nTo assess the programme feasibility, researchers will additional invite art therapist participants to evaluate the programme and invite community staff participants to discuss about the programme implementation.\n\nArt therapist participants will complete programme and session evaluation reports.\n\nCommunity staff participants will attend a focus group discussion.",[228],"Vulnerable Families",[230,231],"Vulnerable families","art therapy","2026-02-20",{"date":234,"type":37},"2026-02-24",{"date":236,"type":37},"2025-02-22",{"date":108,"type":21},{"name":43,"class":44},{"id":240,"slug":241,"hasResults":11,"nctId":242,"briefTitle":243,"officialTitle":244,"acronym":4,"eligibilityCriteria":245,"healthyVolunteers":86,"sex":16,"minAge":17,"maxAge":246,"enrollmentInfo":247,"targetDuration":4,"studyType":22,"phases":249,"briefSummary":250,"conditions":251,"keywords":256,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":262,"lastUpdatePostDateStruct":263,"startDateStruct":265,"completionDateStruct":267,"leadSponsor":269,"locationsCount":4},"100592310","investigating-the-effectiveness-of-a-2-week-novel-non-invasive-brain-stimulation-technique-on-cognitive-outcomes-in-healthy-adults-100592310","NCT06991764","Investigating the Effectiveness of a 2-week Novel Non-invasive Brain Stimulation Technique on Cognitive Outcomes in Healthy Adults","Investigating the Effectiveness of a 2-week High-frequency Transcranial Pulsed-current Stimulation on Cognitive Outcomes in Healthy Adults: A Randomised, Double Blinded, Sham-controlled Study","Inclusion Criteria:\n\n* Male and female young (21 to 30 years) and older adults (60 to 75 years)\n* Right-handed\n* Must be a native English speaker\n* No clinical diagnosis of neurodevelopmental, mood, neurological or neurodegenerative disorders\n* Adults with cardiometabolic or cardiovascular conditions may participate if their condition is controlled and stable with medication and \u002F or lifestyle interventions\n\nExclusion Criteria:\n\n* Currently on long-term medication for pain or migraines \u002F headaches\n* Adults with metallic implants in the chest or head region\n* Adults with epilepsy, or known seizure or immediate family members that have had a seizure before\n* Had a recent head injury that resulted in a temporary loss of consciousness or of memory in the last 12 months\n* Had prior head surgery\n* Prone to fainting\n* Sensitive skin or prone to skin allergies","75 Years",{"count":248,"type":21},120,[24],"The goal of this randomised controlled trial is to investigate the effects of a 2-week high-frequency transcranial pulsed current stimulation (tPCS) on cognitive outcomes in older and healthy adults. The main questions it aims to answer are:\n\n1. Would a single session of anodal tPCS over the left prefrontal cortex improve working memory, task inhibition, and task switching in healthy young and older adults, compared to anodal transcranial direct current stimulation (tDCS) and sham-tPCS?\n2. Would repeated session of anodal-tPCS (2-weeks) lead to improvements in working memory, task inhibition, and task switching in healthy young and older adults, compared to tDCS and sham-tPCS?\n3. Will tPCS be better tolerated among healthy adults, compared to tDCS?\n\nResearchers will compare tPCS \u002F tDCS \u002F sham-tPCS to see if there are any differences in cognitive outcomes after 1 session and after repeated sessions, as well as to compare the tolerance of tPCS against tDCS and sham-tPCS.\n\nParticipants will be requested to:\n\n* Undergo 1 of 3 of the following conditions: tDCS \u002F tPCS \u002F sham-tPCS\n* Complete three sessions of cognitive tasks testing working memory, inhibition and task switching at baseline (pre-stimulation), after day 1 of brain stimulation and after 10 sessions of brain stimulation (post- repeated stimulation)\n* Undergo fNIRS-EEG brain measurements concurrently with the cognitive tasks",[252,253,254,255],"Transcranial Direct Current Stimulation (tDCS)","Ageing","Executive Functioning","Transcranial Electric Stimulation",[257,258,254,259,260,261,253],"Randomised Controlled Trial","Non-Invasive Brain Stimulation","Transcranial Direct Current Stimulation","Transcranial Pulsed Current Stimulation","Healthy Adults","2025-05-18",{"date":264,"type":37},"2025-05-28",{"date":266,"type":21},"2025-06-01",{"date":268,"type":21},"2027-04-30",{"name":43,"class":44},{"id":271,"slug":272,"hasResults":11,"nctId":273,"briefTitle":274,"officialTitle":275,"acronym":4,"eligibilityCriteria":276,"healthyVolunteers":86,"sex":16,"minAge":87,"maxAge":277,"enrollmentInfo":278,"targetDuration":4,"studyType":280,"phases":4,"briefSummary":281,"conditions":282,"keywords":288,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":296,"lastUpdatePostDateStruct":297,"startDateStruct":299,"completionDateStruct":301,"leadSponsor":303,"locationsCount":45},"100575268","brightline-advancing-mental-health-on-campus-100575268","NCT06770075","Brightline: Advancing Mental Health on Campus","Brightline - a Digital Phenotyping Study Toward Advancing Mental Health on Campus","Inclusion Criteria:\n\n* Be aged 18 years or older.\n* Be a current full-time undergraduate student.\n* Own a smartphone with Wi-Fi, 4G, and Bluetooth capabilities.\n* Possess adequate English language proficiency.\n* Be able to download the study apps.\n* Provide informed consent.\n\nExclusion Criteria:\n\n* Are part-time students.\n* Have a current diagnosis of any mental health disorder or a past diagnosis with any bipolar disorder, substance use disorder, or any psychotic disorder.\n* Are currently undergoing mental health treatment.\n* Lack sufficient English proficiency.\n* Report suicidal ideation as indicated by Patient Health Questionnaire (PHQ-9) Item-9, \"Thoughts you would be better off dead or of hurting yourself in some way\".\n* Cannot commit to wearing a wearable device for the six-month monitoring period.\n* Receive special education accommodations or support from the university.","25 Years",{"count":279,"type":21},500,"OBSERVATIONAL","This observational study will employ a multi-modal observation methodology, integrating data from wearable devices and smartphones to establish comprehensive digital biomarkers for identifying symptoms of mental health conditions in university students. The study aims to identify the digital behavioural markers associated with mental health conditions, develop predictive algorithms for mental health states from digital markers, and identify university students at risk for mental health conditions.",[283,124,284,285,286,287],"Depression","Stress","Positive Affect","Negative Affect","Loneliness",[289,290,291,292,293,294,295],"university student","mental health","digital phenotyping","digital biomarkers","passive sensing","risk prediction","mental health seeking","2025-01-13",{"date":298,"type":37},"2025-01-15",{"date":300,"type":21},"2025-01",{"date":302,"type":21},"2026-03",{"name":43,"class":44},{"id":305,"slug":306,"hasResults":11,"nctId":307,"briefTitle":308,"officialTitle":309,"acronym":4,"eligibilityCriteria":310,"healthyVolunteers":86,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":311,"targetDuration":4,"studyType":22,"phases":312,"briefSummary":313,"conditions":314,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":317,"lastUpdatePostDateStruct":318,"startDateStruct":320,"completionDateStruct":322,"leadSponsor":324,"locationsCount":45},"100561929","aspirational-rehabilitation-coaching-for-holistic-health-arch-a-pilot-pre-post-experimental-study-100561929","NCT06596551","Aspirational Rehabilitation Coaching for Holistic Health (ARCH): A Pilot Pre-Post Experimental Study","Aspirational Rehabilitation Coaching for Holistic Health (ARCH): A Pilot Pre-Post Evaluation of Psychosocial Recovery in First-Time Stroke Survivors and Family Caregivers","Inclusion Criteria:\n\n* Aged 21 years and above\n* Recovering from their first stroke at mild to moderate degree of severity\n* Discharged from inpatient care at no later than 3 months,\n* Clinically assessed to have cognitive capacities to engage in and complete the research study,\n* Language capabilities in English or Mandarin, and\n* One identified primary family caregiver aged 21 years and above with similar language capabilities.\n\nExclusion Criteria:\n\n* Families with survivors suffering from aphasia,\n* Being too ill to participate,\n* Experiencing moderate to severe cognitive impairment, and\n* With family caregivers who are not interested to participate.",{"count":20,"type":21},[24],"The ARCH programme is a novel, strength-based, dyadic, multicomponent psychosocial intervention that blends together psychoeducation, psychosocial support and self-compassion practices to aid first-time stroke survivors and their family caregivers with their psycho-socio-emotional and spiritual challenges following discharge from in-patient care. A pre-post experimental design with a feasibility and acceptability assessment is adopted to evaluate and refine the ARCH intervention in promoting wellbeing, self-compassion, independence, quality of life, hope, resilience, self-efficacy and dyadic mutuality.",[201,315,316],"Psychological Well-Being","Psychosocial Functioning","2024-09-11",{"date":319,"type":37},"2024-09-19",{"date":321,"type":37},"2024-03-01",{"date":323,"type":21},"2026-09-01",{"name":43,"class":44},""]