[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100620315":3},{"organization":4,"armGroups":7,"interventions":25,"overallOfficials":30,"centralContacts":39,"locations":45,"responsibleParty":59,"collaborators":30,"id":62,"slug":63,"hasResults":64,"nctId":65,"briefTitle":66,"officialTitle":67,"acronym":30,"eligibilityCriteria":68,"healthyVolunteers":69,"sex":70,"minAge":71,"maxAge":30,"enrollmentInfo":72,"targetDuration":30,"studyType":75,"phases":76,"briefSummary":78,"conditions":79,"keywords":81,"overallStatus":87,"whyStopped":30,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":92,"completionDateStruct":93,"leadSponsor":95,"locationsCount":96},{"fullName":5,"class":6},"Abant Izzet Baysal University","OTHER",[8,14,20],{"label":9,"type":10,"description":11,"interventionNames":12},"Acupressure Group","EXPERIMENTAL","Participants assigned to this group will receive acupressure applied to the HT7, SP6, and ST36 acupoints by a trained researcher. The intervention will be administered once daily for six sessions, with each session lasting approximately 15-20 minutes, in addition to routine clinical care.",[13],"Other: Acupressure",{"label":15,"type":16,"description":17,"interventionNames":18},"Placebo Group","PLACEBO_COMPARATOR","Participants assigned to this group will receive sham acupressure, consisting of light pressure applied to non-acupoint areas near the same anatomical regions as the intervention group. The sham procedure will be administered once daily for six sessions, with each session lasting approximately 15-20 minutes, in addition to routine clinical care. Pressure will be applied on the bone area where the meridians do not pass, parallel to the points where acupressure is applied to the sham points (approximately 1-1.5 cm away).",[19],"Other: Placebo Sham Acupressure",{"label":21,"type":6,"description":22,"interventionNames":23},"Control Group (Routine Care)","Participants assigned to this group will receive routine clinical care only and will not receive any additional intervention during the study period.",[24],"Other: Routine care",[26,31,35],{"type":6,"name":27,"description":28,"armGroupLabels":29,"otherNames":30},"Acupressure","The acupressure intervention will be conducted in a designated room at the institution, once daily for 6 consecutive days, with each session lasting 15-20 minutes, totaling 6 sessions. During the first 3-5 minutes of each session, participants will be guided to the appropriate position and approached to ensure comfort. Acupressure will then be applied to a total of six points: both wrists (HT7) and both legs (ST36, SP6), with two points on each limb. Each of the six points will receive a 30-second preparation followed by 2 minutes of acupressure application",[9],null,{"type":6,"name":32,"description":33,"armGroupLabels":34,"otherNames":30},"Placebo Sham Acupressure","Participants in the placebo group will receive sham acupressure administered by the researcher in a quiet, designated room at the institution, once daily for 6 consecutive days, with each session lasting 15-20 minutes, totaling 6 sessions. Pressure will be applied to bony areas approximately 1.5-2 cm away from the HT7, SP6, and ST36 points, where no meridians pass. Prior to the application, the sham points will be gently warmed and massaged for approximately 20 seconds to reduce tissue sensitivity, preparing the area for the sham acupressure procedure.\n\nIn the intervention group, evaluation will be made at the specified frequency, using the same measurement tools and the same measurement methods.",[15],{"type":6,"name":36,"description":37,"armGroupLabels":38,"otherNames":30},"Routine care","Participants will receive routine clinical care only and no additional intervention.",[21],[40],{"name":41,"role":42,"phone":43,"phoneExt":30,"email":44},"Saadet CAN ÇİÇEK","CONTACT","+905062846936","saadet.cancicek@ibu.edu.tr",[46],{"facility":47,"status":30,"city":48,"state":30,"zip":30,"country":49,"countryCode":30,"cosmosGeoPoint":50,"geoPoint":55,"contacts":56},"Bolu Abant Izzet Baysal University","Bolu","Turkey (Türkiye)",{"type":51,"coordinates":52},"Point",[53,54],31.60611,40.73583,{"lat":54,"lon":53},[57],{"name":58,"role":42,"phone":43,"phoneExt":30,"email":30},"Saadet Can Çiçek",{"type":60,"investigatorFullName":58,"investigatorTitle":61,"investigatorAffiliation":5,"oldNameTitle":30,"oldOrganization":30},"PRINCIPAL_INVESTIGATOR","Associate Professor","100620315","effect-of-acupressure-on-blood-glucose-and-anxiety-in-elderly-with-diabetes-100620315",false,"NCT07356024","Effect of Acupressure on Blood Glucose And Anxiety in Elderly With Diabetes","Effect of Acupressure on Blood Glucose And Anxiety in Elderly With Diabetes: A Three Arm, Parallel Group, Double Blind, A Randomized Controlled Trial","Inclusion Criteria:\n\n* Voluntarily agreeing to participate in the study,\n* Being 65 years of age or older,\n* Having been diagnosed with diabetes for at least one year,\n* Not having any hearing, speech, or vision impairments that would interfere with communication,\n* Being able to speak and understand Turkish,\n* Having a Mini-Mental State Examination (MMSE) score of 23 or higher for literate participants and 19 or higher for illiterate participants,\n* Not using any other complementary or supportive therapies during the study period,\n* Receiving dietary treatment or oral antidiabetic medication for diabetes management,\n* Having no skin irritation, ulceration, or other impairment of skin integrity at the application sites.\n\nExclusion Criteria:\n\n* Initiation of a new medication with potential effects on blood glucose levels in addition to the current treatment during the study period,\n* Use of insulin therapy for diabetes management.",true,"ALL","65 Years",{"count":73,"type":74},48,"ESTIMATED","INTERVENTIONAL",[77],"NA","This study is designed to evaluate the effect of acupressure on blood glucose levels and anxiety in elderly individuals with diabetes. Participants will be assigned to an acupressure intervention group or a control group. The primary outcome of the study is blood glucose level, which will be assessed at baseline and at the end of the intervention period. Secondary outcomes include anxiety levels.",[80,27],"Diabetes Mellitus",[82,83,84,27,85,86],"Randomized Controlled Trial","Diabetes","Elderly","Anxiety","Blood Glucose","NOT_YET_RECRUITING","2026-01-24",{"date":90,"type":91},"2026-01-27","ACTUAL",{"date":88,"type":74},{"date":94,"type":74},"2026-10-27",{"name":5,"class":6},1]