[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Phenikaa University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":77},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,47],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100656557","acupressure-to-improve-insomnia-among-the-elderly-with-hypertension-100656557",false,"NCT07827560","Acupressure to Improve Insomnia Among the Elderly With Hypertension","Self-acupressure to Improve Insomnia Among the Elderly With Hypertension: a Randomized Controlled Trial","Inclusion Criteria:\n\n* Hypertention patient who are ≥ 60 years old\n* Having Insomnia Severity Index score ≥ 11\n* Having Karnofsky score ≥ 80.\n\nExclusion Criteria:\n\n* Patients who are currently participating in clinical trials for the treatment of insomnia.\n* Patients who are currently receiving pharmacological treatment for insomnia.\n* Patients with concomitant cardiovascular conditions, such as heart failure; patients with an implanted pacemaker; patients who have an indication for catheter-based cardiovascular intervention; or patients who have an indication for cardiovascular surgery.\n* Patients with psychiatric disorders, such as depression, generalized anxiety disorder, or bipolar disorder.","ALL","60 Years",{"count":19,"type":20},94,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this study is to evaluate the feasibility and the effect of self-acupressure on improving insomnia among the elderly with hypertension who reported insomnia (using the Insomnia Severity Index questionnaire)\n\nThe main questions it aims to answer are:\n\n* Is the proposed intervention feasible to deliver to the target population in terms of recruitment, retention, adherence, and completion of outcome assessments?\n* Does self-acupressure improve insomnia among the elderly with hypertension? Researchers will compare participants in the self-acupressure group (practice acupressure at home for 28 days) and the enhanced standard care group to see the effectiveness of acupressure in improving insomnia for hypertensive elderly individuals.\n\nParticipants in the self-acupressure group will be instructed how to locate and perform acupressure, then they will be asked to practice acupressure at home for 28 days (once a day).\n\nParticipants in the enhanced standard care group will receive training on how to apply sleep hygiene rules and will be asked to follow sleep hygiene rules for 28 days.",[26,27,28],"Insomnia (Self-reported, Non-diagnosed)","Hypertension","Elder",[30,31,32,33],"acupressure","insomnia","elderly","hypertension","RECRUITING","2026-10-01",{"date":37,"type":38},"2026-10-02","ACTUAL",{"date":40,"type":38},"2026-08-30",{"date":42,"type":20},"2027-03-30",{"name":44,"class":45},"Phenikaa University","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":54,"sex":55,"minAge":56,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":21,"phases":59,"briefSummary":61,"conditions":62,"keywords":64,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":4},"100609255","phase-3-effectiveness-of-10-lidocaine-on-relieving-pain-caused-by-intravenous-intubation-100609255","NCT07212192","Effectiveness of 10% Lidocaine on Relieving Pain Caused by Intravenous Intubation","Effectiveness of 10% Lidocaine Spray on Relieving Local Pain Caused by Intravenous (IV) Intubation: a Randomized Control Trial","Inclusion criteria\n\n* Inclusion criteria comprised participants who were going to undergo a scheduled C-section delivery\n* Over 18 years old\n* Able to read and write Vietnamese.\n* Sign the consent form\n\nExclusion criteria\n\n• Participants who were emergency cases for going to a C-section delivery",true,"FEMALE","18 Years",{"count":58,"type":20},150,[60],"PHASE3","The goal of this clinical trial is to learn if 10% Lidocaine spray can reduce local pain caused by intravenous (IV) intubation among women. The main questions it aims to answer are:\n\n* Does 10% Lidocaine spray lower the VAS score in participants need intravenous intubation?\n* What size effect of 10% Lidocaine spray when patients administered? Researchers will compare 10% Lidocaine spray to a placebo (a look-alike substance that contains no drug) to see if 10% Lidocaine spray works to reduce local pain caused by intravenous (IV) intubation\n\nParticipants will:\n\n* Receive 3 spray of 10% Lidocaine at intravenous catheter insertion site before the nurse perform the IV insert procedure\n* Assess the pain cause by IV insertion using VAS",[63],"Pregnancy",[65,66,67],"Lidocaine","IV pain","C-Section","NOT_YET_RECRUITING","2025-11-23",{"date":71,"type":38},"2025-12-01",{"date":73,"type":20},"2025-11-24",{"date":75,"type":20},"2026-01-25",{"name":44,"class":45},""]