[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"dry-mouth\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:dry-mouth":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,50],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100558738","oral-health-intervention-in-adult-primary-care-100558738",false,"NCT06555029","Oral Health Intervention in Adult Primary Care","Multi-Level Interventions to Reduce Oral Health Disparities Among Adults in Primary Care Settings","Inclusion Criteria:\n\nPractices:\n\n* Use Epic EHR\n* Have older adults covered by Medicaid\n* Located within 60 miles of the CWRU research offices\n\nProvider (medical staff or clinician):\n\nMedical staff (MA, nurse):\n\n* Do not float between practices\n* Plan not to leave practice within a year\n* Provide a signed and dated consent form\n\nClinicians (Physician, NP):\n\n* Have a minimum of 2 patient-care days per week\n* Do not float between practices\n* Plan not to leave practice within a year\n* Provide signed and dated consent form\n\nOlder Adult\u002FPatient Participant:\n\n* Enrolled in CareSource Medicaid Plan\n* Female or male aged 55 years or older\n* Attending non-urgent primary care visits (PCV) at enrolled site\n* Provide signed and dated informed consent form\n* Planning to stay in the immediate area for the next year\n* Enrolled in the Adult Wellness Registry\n\nExclusion Criteria:\n\n* The presence of any serious medical health condition (such as dementia or other cognitive disorder not allowing them to participate) where the clinician indicates they should not participate.\n* The presence of any serious mental health disorders such as schizophrenia where the clinician indicates they should not participate.",true,"ALL","55 Years",{"count":20,"type":21},929,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study is a Stage III cRCT to test the efficacy of multi-level interventions at the practice- and provider-level to address low dental utilization (attendance) among Medicaid-enrolled older adults 55 years or older attending non-urgent primary care visits (PCV) in MetroHealth practice settings. Twelve practices will be randomized into two arms: A) Intervention arm will receive the multi-level intervention that includes: 1. Practice-level: EHR changes to include: ask, advise, assess, and connect (AAAC) strategies; 2. Provider-level: Medical staff (MA, nurse): Training in the AAAC process and complete AAAC for enrolled older adults; Clinicians (physician\u002Fnurse practitioner): CSM-based education (didactic), skills training (video training with standardized patients), and view completed AAAC in EHR to deliver core oral health (OH) facts to older adults, reinforce importance of dental visits, and document in EHR that OH facts were delivered. B) Control arm will receive, at the provider-level only (clinicians), non-theory-based information about retaining a healthy mouth using the ADA Mouth Healthy Series and deliver standard OH care for patients. Older Adults will be followed at 12 months and 24 months to determine if the participant had any dental attendance.\n\nThe primary objective is to test the efficacy of the practice level EHR strategy to ask \\[OH risk assessment\\], advise \\[going to dentist\\], assess \\[willingness for referral\\], and connect \\[eReferral, resources\\] together with clinician theory-based education to communicate OH facts versus clinician alone (standard oral health care) in increasing dental attendance in primary care settings.\n\nThe secondary objectives are to assess oral hygiene behavior, Geriatric Oral Health Quality of life, biometric measures (BP, serum cholesterol, blood glucose, hbA1c) abstracted from EHR data, potential mediators and moderators to investigate pathways that affect the primary and secondary outcomes, and assess implementation strategies: adoption, reach, fidelity, and maintenance of providers and practices that affect older adult primary and secondary outcomes.\n\nThe hypothesis is that medical staff completing the AAAC strategy and clinicians with improved OH knowledge (chronicity, systemic effects) will deliver consistent oral health messaging to older adults at PCVs that will result in increased preventive and restorative dental utilization compared to those providers delivering standard care.",[27,28,29,30],"Dental Caries","Dry Mouth","Periodontal Diseases","Bleeding Gum",[32,33,34,35,36],"Oral Health","Primary Care","Older Adults","Common Sense Model of Self-Regulation","EHR Modifications (Oral Health Questions and Referral)","RECRUITING","2025-10-13",{"date":40,"type":41},"2025-10-15","ACTUAL",{"date":43,"type":41},"2024-09-25",{"date":45,"type":21},"2028-10-30",{"name":47,"class":48},"Case Western Reserve University","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":17,"minAge":57,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":22,"phases":61,"briefSummary":62,"conditions":63,"keywords":65,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":49},"100585304","effects-of-methods-on-dry-mouth-after-septoplasty-surgery-100585304","NCT06900621","Effects of Methods on Dry Mouth After Septoplasty Surgery","Effects of Two Different Methods on Early Period Dry Mouth After Septoplasty Surgery","Inclusion Criteria:\n\n* Age between 18 and 89\n* Able to communicate in Turkish\n* No obstacle to communication\n* Agreeing to participate in the study\n* Conscious and oriented as a result of the evaluation made with SPMT at 30 minutes after the surgery, with a clear airway, no nausea or vomiting\n* Using silicone nasal tampons\n\nExclusion Criteria:\n\n* Patients with a preoperative oral mucous membrane integrity assessment Oral Assessment Guide (OAG) result of over 16\n* Those taking medication that affects dry mouth\n* Those with a chronic disease that affects dry mouth\n* Those undergoing a second simultaneous surgical procedure\n* Those who develop complications during surgery and\u002For during recovery from anesthesia\n* Patients who smoke will not be included in the study.","18 Years","89 Years",{"count":60,"type":21},81,[24],"It was planned to investigate the effects of two different methods on early dry mouth after septoplasty surgery. The data of this study, which is planned to be conducted experimentally, is planned to be collected at Gönen State Hospital between 2025-2026. Patients who are scheduled to undergo septoplasty surgery and present with septum deviation constitute the universe of the study. The research sample (n: 63) was determined using the Power analysis G\\*Power v3.1.9.7 program by taking the sample study as reference. However, considering the data losses (dropouts) in similar studies, when the missing data rate was taken as 20% , the sample size was determined as 81 patients. Patients who were informed about the study and volunteered to participate in the study (n: 81) and met the inclusion criteria of the study will constitute the sample group. 3 groups were determined in the study as intervention groups (group 1 and group 2) and control group (group 3). Patients who meet the preoperative criteria will be randomized into one of three groups after surgery. Data will be collected using the Patient Identification Form, General Patient Follow-up Form, Nasal Obstruction Symptom Assessment Scale (NOSE), Visual Analog Scale (VAS) scoring expressed by the patient to measure mouth dryness and satisfaction, \"Safety Protocol for Thirst Management in the Immediate Postoperative Period\" (SPTM), Oral Mucous Membrane Integrity Assessment and Follow-up Form - Oral Assessment Guide (OAG). 3 groups will be created in the study. 5 ml of ice water will be applied to one group that will receive intervention, the other group will be given water at normal room temperature, and the control group will receive standard clinical care and will not be treated. As a result of the evaluation made with SPTM in the first 30 minutes after the surgery, the dry mouth of all patients included in the study (Group 1, Group 2, Group 3) who meet the conditions will be evaluated before the application, starting from the first 30 minutes after the surgery and at 60 - 90 - 120 - 150 - 180 minutes. In the study, all patients (Group 1, Group 2, Group 3) will be evaluated for dry mouth before the application. The data obtained as a result of the study will be analyzed with a statistical package program. In the evaluation of the data in the study, descriptive statistics and parametric or non-parametric tests will be applied depending on whether the data show a normal distribution. In comparisons, p\\\u003C0.05 value will be considered statistically significant.",[64,28],"Septoplasty",[66,67,68,69,70,71],"dry mouth","nursing","early period","septoplasty","water at room temperature","ice water","NOT_YET_RECRUITING","2025-03-29",{"date":75,"type":41},"2025-04-03",{"date":77,"type":21},"2025-03-25",{"date":79,"type":21},"2027-12-31",{"name":81,"class":48},"Ege University"]