[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"City University of Hong Kong\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":271},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,43,69,96,121,148,173,192,221,243],{"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":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100621748","online-self-healing-program-100621748",false,"NCT07374653","Online Self-healing Program","Online Cognitive Behavioural Therapy for Adolescents With Depression - A Randomized Controlled Trial","iCBT-A","Inclusion Criteria:\n\n1. aged between 12 and 18 years old;\n2. students of a local collaborating secondary school and\u002For youth service units;\n3. having mild to moderate depressive symptoms as assessed with a standardized assessment tool, i.e. Chinese Depression Anxiety Stress Scale (DASS-Y; Cao et al., 2023) with a DASS Depression score of between 7 and 13; and\n4. provide parental consent.\n\nExclusion Criteria:\n\nThose with severe depression (i.e., a DASS Depression score 14 or more) or at risk of suicide are excluded from this study.",true,"ALL","12 Years","18 Years",{"count":22,"type":23},200,"ESTIMATED","INTERVENTIONAL",[26],"NA","Background. Almost two thirds of adolescents experience a mental disorder before the age of 25. Among mental disorders, depression is one of the most common among young people aged between 15 to 24, with a prevalence of 13.5% to 15.8% worldwide and 13.2% in Hong Kong, which is alarming.\n\nCognitive behavioural therapy and online cognitive behavioural therapy has been shown to be effective on reducing depression. Also, online cognitive behavioural therapy has also been shown to be useful for people with mild to moderate depression. However, there is a lack of an effective short-term online cognitive behavioural therapy for adolescents with depression, named online cognitive behavioural therapy in Hong Kong.\n\nObjectives: This study aims to explore the efficacy and effectiveness of a short-term online cognitive behavioural therapy for adolescents with depressive symptoms.\n\nHypothesis:\n\ni. The online cognitive behavioural therapy, as compared to an online relaxation program, is significantly more effective on improving mental health, including reducing anxiety and depressive symptoms, and increasing psychological well-being for participants.\n\niii. The treatment outcomes, as stated in (i), are predicted by individual's uptake, adherence and dropout rate of online cognitive behavioural therapy.\n\nResearch Design. A multicentre blinded randomized controlled two-arm parallel-group trial will be adopted. Participating adolescents will be recruited from collaborating secondary schools. Using block randomization, subjects will be assigned in a 1:1 ratio to an online cognitive behavioural therapy and an online relaxation program. Both online cognitive behavioural therapy and online relaxation program will provide six online modules for participants to learn through computer and\u002For smartphone. Participants will complete the same online assessment tools at pre-intervention, post-intervention, and 2-month follow-up periods.\n\nSubjects Inclusion Criteria. Subjects inclusion criteria includes: (a) aged between 12 and 18 years old; (b) students of a local collaborating secondary school; (c) having mild to moderate depressive symptoms as assessed with a standardized assessment tool, i.e. Chinese Depression Anxiety Stress Scale (DASS-Y; Cao et al., 2023) with a DASS Depression score of between 7 and 13; and (d) provide parental consent. Those with severe depression or at risk of suicide are excluded from this study.\n\nSignificance: This study aims to make a significant contribution to the development of an online cognitive behavioural therapy for Chinese adolescents with depressive symptoms. In particular, the online cognitive behavioural therapy could be used in secondary schools to serve those students with mental health problems who are reluctant to seek help from traditional face-to-face counselling.",[29],"Mild to Moderate Depressive Symptoms","NOT_YET_RECRUITING","2026-04-21",{"date":33,"type":34},"2026-04-24","ACTUAL",{"date":36,"type":23},"2026-09-01",{"date":38,"type":23},"2027-08-31",{"name":40,"class":41},"City University of Hong Kong","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":17,"sex":18,"minAge":20,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":24,"phases":54,"briefSummary":55,"conditions":56,"keywords":58,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":64,"startDateStruct":65,"completionDateStruct":66,"leadSponsor":68,"locationsCount":42},"100623130","mindfulcityu---a-mindfulness-mobile-application-for-promoting-university-students-mental-health-100623130","NCT07392632","MindfulCityU-- A Mindfulness Mobile Application for Promoting University Students' Mental Health","MindfulCityU: Implementation and Evaluation of a Mindfulness Mobile Application for Promoting University Students' Mental Health","MindfulCityU","Inclusion Criteria:\n\n(i) current undergraduate or postgraduate students; (ii) aged 18-30 years; (iii) possessing smartphone ownership and reliable internet access necessary for intervention engagement; (iv) having a score between 10-23 on the DASS-Y Depression subscale indicating a mild to moderate depressive symptom; and (v) provide informed consent\n\nExclusion Criteria:\n\n(i) students currently engaged in formal mindfulness training exceeding one session per week will be excluded to prevent confounding effects from concurrent mindfulness practice; (ii) those scoring above 23 on the DASS-Y Depression subscale, indicating severe symptoms, will be excluded and referred to appropriate clinical services to ensure their safety and access to needed care; (iii) students reporting active suicidal ideation or self-harm behaviors will be immediately referred to crisis intervention services and excluded from study participation to prioritize their safety; (iv) current engagement in psychotherapy or recent medication changes within the previous four weeks; (v) students planning to leave the university during the study period.","30 Years",{"count":53,"type":23},120,[26],"The research aims to investigate the effectiveness a mobile phone application-based (app-based) mindfulness interventions for university students with mild depressive symptoms.\n\nThis study adopts a multicentre randomized control trial two arms research design. A randomised controlled trial will compare a newly designed mobile phone application-based (app-based) mindfulness interventions, named MindfulCityU, with a waitlist control group to determine whether the MindfulCityU produces better intervention outcomes on promoting mental health for university students, including depressive symptoms, mindfulness, and wellbeing. The MindfulCityU provides 8 online modules on mindfulness for participants to access and learn at home through their smartphones and\u002For computer. Participants of waitlist control group participants receive no active intervention at the initial stage and receive the same MindfulCityU at a later stage.\n\nParticipants will complete online standardized assessment tools on their intervention outcomes before and after the intervention and 2-months follow-up. The ethical considerations of this study were reviewed and approved by the Human and Artefacts Ethics Sub-Committee of the City University of Hong Kong in 2025.",[57],"Depressive Symptoms",[59,60,61,62,63],"Digital Mental Health Intervention","Mobile phone application-based","Mindfulness-based Intervention","Depression","Mindfulness",{"date":33,"type":34},{"date":36,"type":23},{"date":67,"type":23},"2027-06-30",{"name":40,"class":41},{"id":70,"slug":71,"hasResults":11,"nctId":72,"briefTitle":73,"officialTitle":73,"acronym":74,"eligibilityCriteria":75,"healthyVolunteers":11,"sex":18,"minAge":76,"maxAge":4,"enrollmentInfo":77,"targetDuration":4,"studyType":24,"phases":79,"briefSummary":80,"conditions":81,"keywords":82,"overallStatus":89,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":90,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":42},"100621543","efficacy-of-narrative-therapy-for-older-people-with-depression-100621543","NCT07371988","Efficacy of Narrative Therapy for Older People With Depression","NTOPD","Inclusion Criteria:\n\n1. aged 60 years or above;\n2. exhibiting depressive symptoms as assessed using a standardised assessment tool, namely the Chinese Beck Depression Inventory-II (BDI; Byrne et al., 2004), with a BDI score between 10 and 30;\n3. being a service user of an elderly centre; and\n4. providing informed consent to participate in this research.\n\nExclusion Criteria:\n\n1. Individuals with severe depression (i.e. a BDI score ≥ 31), dementia, psychosis, or self-reported suicidal thoughts are excluded from this study; and\n2. Individuals currently receiving a therapeutic intervention are not excluded from this study.","60 Years",{"count":78,"type":23},110,[26],"The research aims to investigate the efficacy of a narrative therapy group in reducing depressive symptoms among older people.\n\nThis study adopts a mixed methods research design, involving both quantitative and qualitative approaches. In the quantitative study, a randomised controlled trial will compare a narrative therapy group with a waitlist control group to determine whether an eight-session narrative therapy group can reduce depressive symptoms in older people. The eight-session narrative therapy group will be delivered by a trained and experienced social worker or counsellor, and intervention outcomes will be assessed before and after the intervention using a standardised assessment tool for depressive symptoms. The qualitative study aims to examine the benefits, advantages, and limitations of the narrative therapy group from the users' perspective.",[62],[83,84,85,86,87,88],"Randomized controlled trial","Depressive Disorders","Narrative Therapy group","Self-stigma","Hope","Wellbeing","RECRUITING",{"date":33,"type":34},{"date":92,"type":34},"2025-11-10",{"date":94,"type":23},"2026-08-31",{"name":40,"class":41},{"id":97,"slug":98,"hasResults":11,"nctId":99,"briefTitle":100,"officialTitle":101,"acronym":102,"eligibilityCriteria":103,"healthyVolunteers":17,"sex":18,"minAge":76,"maxAge":4,"enrollmentInfo":104,"targetDuration":4,"studyType":24,"phases":105,"briefSummary":106,"conditions":107,"keywords":109,"overallStatus":89,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":115,"startDateStruct":116,"completionDateStruct":118,"leadSponsor":120,"locationsCount":42},"100621549","cognitive-stimulation-therapy-group-for-residential-home-residents-with-dementia-and-mild-cognitive-impairment-100621549","NCT07372066","Cognitive Stimulation Therapy Group for Residential Home Residents With Dementia and Mild Cognitive Impairment","Effectiveness of Cognitive Stimulation Therapy Group for Residential Home Residents With Dementia and Mild Cognitive Impairment-- A Randomized Controlled Trial","CSTSAGE","Inclusion Criteria:\n\n1. age 60 years or older;\n2. diagnosis of MCI or dementia according to the Diagnostic and Statistical Manual of Mental Disorder (Fifth edition, Text Revision).\n\nRemark: Participants who do not receive a diagnosis of MCI or dementia will undergo a screening assessment by a researcher using the Chinese Montreal Cognitive Assessment (MoCA)-5 minutes.\n\nExclusion Criteria:\n\nThose who are unable to participate independently in group activities, who exhibit disruptive behavior and\u002For are severely impaired by physical disabilities (e.g. severe hearing and visual impairment) and physical illnesses (e.g. frequent hospital stays) are excluded.",{"count":78,"type":23},[26],"The research aims to investigate the effectiveness a cognitive stimulation therapy group for older adults with dementia and mild cognitive impairment living in residential homes.\n\nThis study adopts a multicenter randomized control trial two arms research design. The randomized controlled trial will compare a typical 14-session cognitive stimulation therapy group with a calligraphy group to determine whether the 14-session cognitive stimulation therapy group can produce better intervention outcomes for older adults with dementia and mild cognitive impairment, including cognitive functions, depressive symptoms, activities engagement, social functioning and, quality of life.",[108],"Cognitive Functions",[110,111,112,113,114],"Cognitive Stimulation Therapy","Calligraphy group","Randomized Controlled trial","Mild cognitive impairment","Dementia",{"date":33,"type":34},{"date":117,"type":34},"2026-01-01",{"date":119,"type":23},"2026-09-30",{"name":40,"class":41},{"id":122,"slug":123,"hasResults":11,"nctId":124,"briefTitle":125,"officialTitle":126,"acronym":127,"eligibilityCriteria":128,"healthyVolunteers":17,"sex":18,"minAge":76,"maxAge":4,"enrollmentInfo":129,"targetDuration":4,"studyType":24,"phases":130,"briefSummary":131,"conditions":132,"keywords":134,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":140,"lastUpdatePostDateStruct":141,"startDateStruct":143,"completionDateStruct":145,"leadSponsor":147,"locationsCount":42},"100635160","multicomponent-intervention-to-improve-cognitive-abilities-in-older-adults-with-mild-cognitive-impairment-100635160","NCT07549074","Multicomponent Intervention to Improve Cognitive Abilities in Older Adults With Mild Cognitive Impairment","Multicomponent Intervention With Healthy Lifestyle Psychoeducation and Cognitive Stimulation to Improve Cognitive Abilities in Older Adults With Mild Cognitive Impairment-A Double-blind Randomized Control Trial","MMI for MCI","The inclusion criteria:\n\n1. age 60 years or older;\n2. diagnosis of MCI or mild neurocognitive disorder according to the Diagnostic and Statistical Manual of Mental Disorder (Fifth edition, Text Revision) (American Psychiatric Association, 2022); Participants who are not diagnosed with MCI will undergo a screening assessment by a research assistant using both the Montreal Cognitive Assessment (MoCA) (Chinese version) with a total score of 19 to 21 represents MCI. (Yeung et al., 2014);\n3. awareness of memory loss with memory complaints;\n4. member of collaborating elderly centre;\n5. able to participate independently in group activities; and\n6. fluent in Cantonese.\n\nThe exclusion criteria:\n\nThose diagnosed with dementia, unable to participate independently in group activities, exhibiting disruptive behavior and\u002For severely impaired by physical disabilities (e.g. a severe hearing problem) are excluded.",{"count":22,"type":23},[26],"The research aims to investigate the effectiveness of a new short-term multicomponent intervention to promote the bio-psycho-social-spiritual health of older adults with MCI to improve their cognitive abilities.\n\nIn this study, the multicomponent intervention consists of healthy lifestyle psychoeducation and cognitive stimulation. This study is a double-blind, clustered, randomized, controlled, four-arm parallel group study. 200 eligible older adults with MCI are openly recruited into activity groups in local elderly centres. The activity groups are randomly allocated to three intervention groups (i.e., multicomponent intervention, cognitive stimulation and lifestyle psychoeducation) and a control group in a 1:1:1:1 ratio. The participants with MCI are blinded on group allocation and kept uninformed which type of intervention they are receiving. An investigator, blinded to group allocation and intervention, assess outcomes using standardized assessment tools before and after the intervention and after 3 months.",[133],"Mild Cognitive Impairment (MCI)",[135,136,137,138,139],"Mild Cognitive Impairment","Double-blind Randomized Controlled Trial","Multicomponent intervention","healthy lifestyle","cognitive stimulation","2026-04-18",{"date":142,"type":34},"2026-04-23",{"date":144,"type":23},"2026-10-01",{"date":146,"type":23},"2028-06-30",{"name":40,"class":41},{"id":149,"slug":150,"hasResults":11,"nctId":151,"briefTitle":152,"officialTitle":153,"acronym":154,"eligibilityCriteria":155,"healthyVolunteers":17,"sex":18,"minAge":156,"maxAge":157,"enrollmentInfo":158,"targetDuration":4,"studyType":24,"phases":159,"briefSummary":160,"conditions":161,"keywords":163,"overallStatus":89,"whyStopped":4,"lastUpdateSubmitDate":167,"lastUpdatePostDateStruct":168,"startDateStruct":169,"completionDateStruct":170,"leadSponsor":172,"locationsCount":42},"100635113","playback-theatre-program-for-adolescents-and-youth-100635113","NCT07548463","Playback Theatre Program for Adolescents and Youth","Playback Theatre Program on Improving Mental Health for Adolescents and Youth","Playback","Inclusion Criteria:\n\n1. aged between 13 to 24 years;\n2. having mild to moderate depression and\u002For anxiety as assessed using a standardized assessment tool, i.e. Chinese Depression Anxiety Stress Scale-Youth (DASS-Y) with a DASS-Y Depression score between 5 and 12;\n3. service users of The Salvation Army social service unit; and\n4. giving informed consent to this research work. For those aged below 18, parental consent will be obtained.\n\nExclusion Criteria:\n\nThose with severe depression (i.e. a DASS-Y Depression score ≥ 13) and\u002For severe anxiety (i.e. a DASS-Y Anxiety score ≥ 8) are excluded from this study.","13 Years","24 Years",{"count":53,"type":23},[26],"The research aims to investigate the effectiveness of playback theatre program on improving mental health for adolescents and youth.\n\nThis study adopts a multicentre randomized control trial two arms research design. A randomised controlled trial will compare a typical 7-session therapeutic song-writing program with a waitlist-control group to determine whether the 7-session playback theatre program can produce better outcomes for young people with depressive symptoms, including improvement in depressive symptoms, self-stigma, self-esteem, sense of hope and social support at post-intervention. The 7-session playback theatre program will be delivered by trained and experienced social workers and helping professionals who are familiar with music therapy. A research staff, who does not involve in the group allocation and delivery of group intervention, conduct the intervention outcomes assessment of the participants before and after the intervention. Standardized assessment tools are used to assess the intervention outcomes. The ethical considerations of this study were reviewed and approved by the Human and Artefacts Ethics Sub-Committee of the City University of Hong Kong in 2026.",[162],"Depresssion",[164,62,165,86,87,166],"Young people","Playback theatre","Randomized Control Trial","2026-04-17",{"date":142,"type":34},{"date":36,"type":23},{"date":171,"type":23},"2027-10-31",{"name":40,"class":41},{"id":174,"slug":175,"hasResults":11,"nctId":176,"briefTitle":177,"officialTitle":178,"acronym":179,"eligibilityCriteria":155,"healthyVolunteers":17,"sex":18,"minAge":156,"maxAge":157,"enrollmentInfo":180,"targetDuration":4,"studyType":24,"phases":181,"briefSummary":182,"conditions":183,"keywords":184,"overallStatus":89,"whyStopped":4,"lastUpdateSubmitDate":167,"lastUpdatePostDateStruct":186,"startDateStruct":188,"completionDateStruct":190,"leadSponsor":191,"locationsCount":42},"100621541","sound-bite---a-therapeutic-song-writing-program-100621541","NCT07371962","Sound Bite-- a Therapeutic Song-writing Program","\"Everyone is a Hope Builder\" Project Study- Therapeutic Song-writing Program","Sound Bite",{"count":53,"type":23},[26],"The research aims to investigate the effectiveness of the therapeutic song-writing program on young people with depressive symptoms.\n\nThis study adopts a multicentre randomized control trial two arms research design. A randomised controlled trial will compare a typical 7-session therapeutic song-writing program with a waitlist-control group to determine whether the 7-session therapeutic song-writing program can produce better outcomes for young people with depressive symptoms, including improvement in depressive symptoms, self-stigma, self-esteem, sense of hope and social support at post-intervention. The 7-session therapeutic song-writing program will be delivered by trained and experienced social workers and helping professionals who are familiar with music therapy. A research staff, who does not involve in the group allocation and delivery of group intervention, conduct the intervention outcomes assessment of the participants before and after the intervention. Standardized assessment tools are used to assess the intervention outcomes. The ethical considerations of this study were reviewed and approved by the Human and Artefacts Ethics Sub-Committee of the City University of Hong Kong in 2025.",[62],[164,62,185,86,87,166],"Therapeutic song-writing",{"date":187,"type":34},"2026-04-22",{"date":189,"type":23},"2026-07-17",{"date":171,"type":23},{"name":40,"class":41},{"id":193,"slug":194,"hasResults":11,"nctId":195,"briefTitle":196,"officialTitle":197,"acronym":4,"eligibilityCriteria":198,"healthyVolunteers":17,"sex":18,"minAge":199,"maxAge":4,"enrollmentInfo":200,"targetDuration":4,"studyType":24,"phases":202,"briefSummary":203,"conditions":204,"keywords":208,"overallStatus":89,"whyStopped":4,"lastUpdateSubmitDate":213,"lastUpdatePostDateStruct":214,"startDateStruct":216,"completionDateStruct":218,"leadSponsor":220,"locationsCount":42},"100603403","jockey-club-support-project-100603403","NCT07136064","Jockey Club Support Project","Jockey Club Support Project to Enhance Emotion Regulation Skills and Resilience of Cross-Boundary Families: A Randomized Controlled Trial","Inclusion Criteria for Parents:\n\n1. have at least one child between the fifth and twelfth grade;\n2. can participate in the intervention with their child;\n3. are Hong Kong residents or have a family member who is a Hong Kong resident;\n4. live in Shenzhen.\n\nInclusion Criteria for Children:\n\n1. are between the fifth and twelfth grade;\n2. are Hong Kong residents or have a family member who is a Hong Kong resident;\n3. live in Shenzhen.\n\nExclusion Criteria:\n\n(a) those who have current diagnoses of severe physical or mental illnesses;","10 Years",{"count":201,"type":23},450,[26],"Guided by the process model of emotion regulation, integrative affect-regulation framework for resilience, and the reciprocal dynamics of emotion, affect, and resilience in the family system, researchers will develop a parallel intervention to incorporate two key members in Mainland-Hong Kong cross-boundary families: a parent and a child by improving their affect\u002Femotion regulation skills, de-escalate family conflicts, and flourish under hardships. Specifically, researchers predict that participants in the intervention group will report greater improvement in resilience, emotion regulation, psychological well-being, family harmony, and social connectedness than those in the control group.",[205,206,207],"Family Relations","Resilience","Emotion Regulation",[209,210,211,212],"cross-boundary families","resilience","emotion regulation","randomized controlled trial","2026-02-10",{"date":215,"type":34},"2026-02-12",{"date":217,"type":34},"2025-11-15",{"date":219,"type":23},"2028-08",{"name":40,"class":41},{"id":222,"slug":223,"hasResults":11,"nctId":224,"briefTitle":225,"officialTitle":226,"acronym":4,"eligibilityCriteria":227,"healthyVolunteers":17,"sex":228,"minAge":20,"maxAge":4,"enrollmentInfo":229,"targetDuration":4,"studyType":24,"phases":231,"briefSummary":232,"conditions":233,"keywords":4,"overallStatus":89,"whyStopped":4,"lastUpdateSubmitDate":235,"lastUpdatePostDateStruct":236,"startDateStruct":238,"completionDateStruct":240,"leadSponsor":241,"locationsCount":242},"100565265","we-intervention-among-chinese-hiv-serodiscordant-male-couples-100565265","NCT06639932","We-INtervention Among Chinese HIV-serodiscordant Male Couples","Evaluating the Effects of the We-INtervention Among Chinese HIV-serodiscordant Male Couples in a Randomized Controlled Trial","Inclusion criteria:\n\n1. both partners are male,\n2. both partners are aged 18 or above,\n3. both partners report being in a committed relationship for at least 3 months,\n4. one partner is HIV-seropositive and the other partner is HIV-seronegative (i.e., serodiscordant couple),\n5. both partners have disclosed their serostatus to each other, and\n6. both partners are willing to participate in this study.\n\nExclusion criteria:\n\n1. either partner is unable to complete the assessment due to a low education level or to physical or psychological constraints and\n2. either partner has been diagnosed with another chronic disease (e.g., cancer and coronary heart disease).","MALE",{"count":230,"type":23},320,[26],"HIV-serodiscordant male couples, in which one male partner is HIV-seropositive and the other is HIV-seronegative, experience multiple risks in HIV care and prevention. As stigma often hinders such couples' access to support and services, leveraging their relational resources is crucial for optimizing their outcomes. The proposed study will assess the efficacy of the three-session We-INtervention focusing on their relationship dynamics to enhance Chinese HIV-serodiscordant male couples' health and well-being.\n\nA total of 160 Chinese HIV-serodiscordant male couples (320 individuals: 160 HIV-seropositive and 160 HIV-seronegative) will be randomized at a 1:1 ratio to either the intervention or control arm. In the intervention arm, the We-INtervention will be delivered to both partners of each couple separately. In the control arm, each couple will receive health information pamphlets.",[234],"HIV","2026-01-18",{"date":237,"type":34},"2026-01-21",{"date":239,"type":34},"2025-09-01",{"date":67,"type":23},{"name":40,"class":41},4,{"id":244,"slug":245,"hasResults":11,"nctId":246,"briefTitle":247,"officialTitle":247,"acronym":4,"eligibilityCriteria":248,"healthyVolunteers":11,"sex":249,"minAge":20,"maxAge":250,"enrollmentInfo":251,"targetDuration":4,"studyType":24,"phases":253,"briefSummary":254,"conditions":255,"keywords":259,"overallStatus":89,"whyStopped":4,"lastUpdateSubmitDate":263,"lastUpdatePostDateStruct":264,"startDateStruct":266,"completionDateStruct":268,"leadSponsor":270,"locationsCount":42},"100606542","doppler-ultrasound-guided-angiopuncture-for-dysmenorrhea-pain-a-clinical-trial-100606542","NCT07176910","Doppler Ultrasound-Guided Angiopuncture for Dysmenorrhea Pain: A Clinical Trial","Inclusion Criteria:\n\nPrimary dysmenorrhea diagnosis (≥6 months of menstrual pain scoring ≥2 on numerical rating scale) Regular menstrual cycles (28-32 days), menstrual period lasts 4 to 7 days No pelvic pathology on transvaginal ultrasound.\n\nExclusion Criteria:\n\ncoagulopathy (INR \\>1.5) recent analgesic use (48-hour washout) secondary dysmenorrhea confirmed by laparoscopy.","FEMALE","25 Years",{"count":252,"type":23},30,[26],"the study is to evaluated dopplar guided angiopuncture efficacy and safety in patients with dysmenorrhea",[256,257,258],"Angiopuncture","Dysmenorrhea","Dopplar Ultrasound",[257,260,261,262],"angiopuncture","dopplar","ultrasound","2025-09-12",{"date":265,"type":34},"2025-09-16",{"date":267,"type":34},"2024-09-01",{"date":269,"type":23},"2025-11-01",{"name":40,"class":41},""]