[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"patient-compliance\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:patient-compliance":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,46,83,110,138,166],{"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},"100523181","effect-of-questionnaires-and-feedback-on-the-patient-compliance-for-endoscopic-surveillance-after-esd-100523181",false,"NCT06092281","Effect of Questionnaires and Feedback on the Patient Compliance for Endoscopic Surveillance After ESD","Effect of Questionnaires and Feedback on the Patient Compliance for Endoscopic Surveillance After Endoscopic Submucosal Dissection: a Prospective, Randomized Controlled, Superiority Trial.","Inclusion Criteria:\n\n* Adult patients (≥18 years) after ESD for mucosal lesions.\n\nExclusion Criteria:\n\n* Patients after ESD for submucosal tumors, e.g. stromal tumors, neuroendocrine tumors;\n* Additional radical surgery after ESD procedure;\n* Past history of ESD procedure or local recurrence;\n* Severe comorbidities with a life expectancy of \\\u003C6 months as judged by the investigator;\n* Unable to cooperate with information collection due to mental disorders, severe neurosis, or dysgnosia;\n* Unable to understand or unwilling to sign a written informed consent.","ALL","18 Years","80 Years",{"count":20,"type":21},500,"ESTIMATED","INTERVENTIONAL",[24],"NA","Endoscopic submucosal dissection (ESD) is now considered the standard treatment for early gastrointestinal neoplasms. However, there is still a possibility of developing local recurrence or metachronous neoplasia after ESD. Regular endoscopic surveillance after ESD can identify and remove local recurrences and metachronous lesions early, improving patient prognosis. However, the patient compliance with post-ESD endoscopic surveillance is currently unclear, and many patients fail to adhere to the scheduled follow-up. A prospective, randomized controlled, superiority trial was designed to evaluate whether completing a questionnaire and receiving feedback on compliance-related education can improve patient compliance with post-ESD endoscopic surveillance, in comparison to those who did not complete the compliance-related education questionnaire. Additionally, the investigators intend to investigate the factors that influence patient compliance.\n\nThis study will consist of two parts.\n\nPart 1 will assess whether the completion of questionnaire and feedback on compliance-related education can improve short-term patient compliance with post-ESD endoscopic surveillance, and investigate factors influencing short-term patient compliance.\n\nPart 2 will assess whether the completion of questionnaire and feedback on compliance-related education can improve long-term patient compliance with post-ESD endoscopic surveillance, and investigate factors influencing patient compliance.",[27],"Patient Compliance",[29,30,31,32],"compliance","endoscopic submucosal dissection","surveillance","post-ESD","RECRUITING","2026-08-14",{"date":36,"type":37},"2026-08-17","ACTUAL",{"date":39,"type":37},"2023-10-01",{"date":41,"type":21},"2029-12",{"name":43,"class":44},"Xijing Hospital of Digestive Diseases","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":22,"phases":56,"briefSummary":57,"conditions":58,"keywords":61,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":45},"100650798","effectiveness-of-telephonic-and-digital-postoperative-follow-up-communication-strategies-on-patient-compliance-clinical-recovery-and-quality-of-life-after-dental-extraction-100650798","NCT07751822","Effectiveness of Telephonic and Digital Postoperative Follow-up Communication Strategies on Patient Compliance, Clinical Recovery, and Quality of Life After Dental Extraction","Effectiveness of Telephonic and Digital Postoperative Follow-up Communication Strategies on Patient Compliance, Clinical Recovery, and Oral Health-related Quality of Life Following Dental Extraction","CONNECT","Inclusion Criteria - Participants must meet all of the following criteria:\n\nAdults aged 18 years or older. Patients undergoing simple or surgical dental extraction under local anesthesia at the Department of Oral and Maxillofacial Surgery.\n\nAble to understand and communicate in Arabic or English. Own a smartphone with access to a mobile messaging application (e.g., WhatsApp) and be able to receive telephone calls.\n\nWilling and able to provide written informed consent. Willing to comply with the study protocol and attend the scheduled postoperative follow-up visits.\n\nExclusion Criteria - Participants meeting any of the following criteria will be excluded:\n\nPatients younger than 18 years of age. Patients unable to provide informed consent. Patients with cognitive impairment, psychiatric illness, or neurological disorders that may interfere with understanding or complying with postoperative instructions.\n\nPatients with hearing or speech impairment preventing effective telephone communication.\n\nPatients without access to a smartphone or unable to use mobile messaging applications independently.\n\nPatients requiring hospital admission following dental extraction. Patients undergoing extraction under general anesthesia. Patients who are unwilling or unable to complete the scheduled follow-up assessments.\n\nPatients participating in another clinical trial that may influence postoperative recovery or study outcomes.",{"count":55,"type":21},216,[24],"Effectiveness of Telephonic and Digital Postoperative Follow-up Communication Strategies on Patient Compliance, Clinical Recovery, and Oral Health-related Quality of Life Following Dental Extraction\n\n(CONNECT Study - CONtinuous post-operative NETwork Communication to Enhance Compliance after Tooth Extraction)\n\nTooth extraction is one of the most commonly performed dental procedures. Although most patients recover uneventfully, complications such as pain, swelling, bleeding, infection, and dry socket may occur if postoperative instructions are not followed correctly. Dentists routinely provide verbal and written instructions after tooth extraction; however, patients may forget or misunderstand these instructions once they leave the clinic, resulting in reduced compliance and delayed recovery.\n\nPrevious research conducted at our institution demonstrated that postoperative telephone follow-up improved patient compliance with post-extraction instructions compared with routine verbal and written instructions alone. Building on these findings, the present study aims to evaluate whether different methods of postoperative communication-including telephone calls, digital messaging, and a combination of both-can further improve patient compliance and clinical recovery following dental extraction.\n\nParticipants undergoing routine dental extraction will receive the standard postoperative verbal and written instructions provided by the Department of Oral and Maxillofacial Surgery. Depending on the assigned study group, participants may also receive structured telephone follow-up, digital communication via a secure messaging platform, or both during the early postoperative period. The information provided through these communication methods will reinforce the same postoperative instructions routinely given in the clinic and will not alter the clinical treatment received.\n\nParticipants will be followed for one week after the extraction. Information will be collected regarding their adherence to postoperative instructions, pain levels, occurrence of complications such as dry socket, and oral health-related quality of life using validated questionnaires. These assessments will help determine whether additional postoperative communication improves patient recovery and overall treatment outcomes.\n\nThe study involves minimal risk because the communication methods are intended only to reinforce standard postoperative care and provide patients with an opportunity to clarify any concerns they may have during recovery. Participation in the study is entirely voluntary, and patients may withdraw at any time without affecting the quality of their dental treatment.\n\nThe findings of this study are expected to provide evidence on the most effective postoperative communication strategy following dental extraction. This may help improve patient education, enhance compliance with postoperative instructions, reduce preventable complications, and support the integration of digital communication technologies into routine dental practice.",[59,60,27],"Tooth Extraction","Postoperative Care",[62,63,27,64,65,66,67,68,69,70,71,72],"Dental Extraction","Postoperative Follow-up","Telephonic Follow-up","Digital Health","WhatsApp","Patient Education","Oral Surgery","Randomized Controlled Trial","Oral Health-related Quality of Life","Postoperative Pain","Dry Socket","NOT_YET_RECRUITING","2026-08-03",{"date":76,"type":37},"2026-08-07",{"date":78,"type":21},"2026-08-06",{"date":80,"type":21},"2027-07",{"name":82,"class":44},"King Saud University",{"id":84,"slug":85,"hasResults":11,"nctId":86,"briefTitle":87,"officialTitle":87,"acronym":4,"eligibilityCriteria":88,"healthyVolunteers":89,"sex":16,"minAge":90,"maxAge":4,"enrollmentInfo":91,"targetDuration":4,"studyType":22,"phases":93,"briefSummary":94,"conditions":95,"keywords":98,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":45},"100635636","reminder-strategies-to-improve-meal-logging-adherence-100635636","NCT07555262","Reminder Strategies to Improve Meal-Logging Adherence","Inclusion Criteria:\n\n* Citizens or residents of Switzerland who are German-speaking (main place of living or employment in Switzerland).\n* Age ≥45 years.\n* BMI ≥25 kg\u002Fm² (overweight or obese).\n* Regular access to a smartphone (iOS or Android) with a data plan.\n* Able to use smartphone applications.\n* Able to walk independently.\n\nExclusion Criteria:\n\n* History of stroke, heart disease, renal failure, cancer, or diabetes (type 1 or type 2).\n* Past vascular bypass surgery or angioplasty.\n* Current or planned use of glucose-lowering medications during the upcoming 4 weeks (e.g., GLP-1 receptor agonists, metformin).\n* Pregnant or breastfeeding.\n* Relevant skin conditions at wearable placement sites (e.g., upper arm).\n* BMI \\\u003C25 kg\u002Fm² confirmed at enrollment.\n* FPG ≥7.0 mmol\u002FL and\u002For HbA1c ≥6.5% (newly identified type 2 diabetes); Individuals who meet type-2 diabetes criteria at enrollment, based on Swiss\u002FADA diagnostic criteria will be informed of blood test results and referred to a GP. These individuals will be deemed ineligible and excluded from the study.",true,"45 Years",{"count":92,"type":21},200,[24],"This study is a single-center micro-randomized trial, aiming to examine the effects of two theory-driven reminder strategies on adherence to repeated, image-based meal logging in adults age 45 and older. Three times daily, participants are automatically randomized to receive one of three reminder messages prior to each habitual mealtime. The main research questions the trial aims to answer are:\n\n* Do loss-framed reminders (emphasizing loss of a daily financial reward for not logging) increase meal logging adherence in the two hours following a reminder, compared to a neutral reminder?\n* Do logging consistency reminders (providing feedback on recent logging streaks) increase meal logging adherence in the two hours following a reminder, compared to a neutral reminder?\n* Do the effects of loss-framed and logging consistency reminders differ from each other?\n\nPrimary aim: To estimate the proximal effect of each reminder type on whether a participant logs a meal within two hours of receiving a reminder.\n\nSecondary aim: To examine whether within-person physiological patterns (e.g., heart rate variation) moderate response to reminders, with the goal of identifying physiological markers of receptivity to behavioral prompts.\n\nThe trial aims to enroll 200 adults aged 45 and older. Participants attend a baseline visit for onboarding, consent, and device setup, followed by a 28 day remote intervention period during which they should photograph their meals three times daily (breakfast, lunch, dinner) and wear a smartwatch and smart ring continuously. Prior to each mealtime, they receive an automatically randomized reminder message. Participants earn a daily financial reward contingent on completing meal logging for that day.\n\nNote: This trial was registered retrospectively as enrollment began prior to registration. However, registration was completed before data collection was finished and before any data analysis was conducted.",[27,96,97],"Mobile Applications","Reminder Systems",[99,100],"micro-randomized trial","adherence","2026-04-28",{"date":103,"type":37},"2026-05-05",{"date":105,"type":37},"2025-12-08",{"date":107,"type":21},"2027-01",{"name":109,"class":44},"University of St.Gallen",{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":114,"acronym":4,"eligibilityCriteria":115,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":116,"targetDuration":4,"studyType":22,"phases":118,"briefSummary":119,"conditions":120,"keywords":123,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":128,"lastUpdatePostDateStruct":129,"startDateStruct":131,"completionDateStruct":133,"leadSponsor":135,"locationsCount":137},"100604055","the-effectiveness-of-neurobot-in-alleviating-anxiety-of-patients-undergoing-neurovascular-surgeries-100604055","NCT07144540","The Effectiveness of NeuroBot in Alleviating Anxiety of Patients Undergoing Neurovascular Surgeries","Inclusion Criteria:\n\n1. aged above 18 years;\n2. scheduled for elective neuroendovascular surgery;\n3. able to understand Chinese and read Chinese;\n4. mobile device with internet capability.\n\nExclusion Criteria:\n\n1. identified cognitive impairment or have difficulty in understanding study procedures, following instructions, or providing informed consent;\n2. prior exposure to health chatbot to acquire health-related information in previous 3 months;\n3. have neurovascular surgeries before",{"count":117,"type":21},146,[24],"The goal of this randomized controlled trial is to investigate the effectiveness of NeuroBot in alleviating anxiety of patients undergoing neurovascular procedures. The main questions it aims to answer are:\n\nIs NeuroBot effective in alleviating anxiety? Is NeuroBot effective in enhancing patients' procedure and disease-related knowledge? Is NeuroBot effective in enhancing patients' compliance to treatment? If there is a comparison group: Researchers will compare with standard perioperative education (control group) to see if there is any difference in results.\n\nParticipants will be invited to chat with the artificial intelligence based chatbot \"NeuroBot\" for 6 weeks, from the date of preoperative clinic visit till 4 weeks after the surgery. The participants are allowed to access the NeuroBot at anytime anywhere, to ask surgery- related questions at their discretion.",[121,27,122],"Anxiety","Knowledge",[124,125,126,127],"Chatbot","NeuroBot","Perioperative education","Neurovascular surgery","2025-08-25",{"date":130,"type":37},"2025-08-27",{"date":132,"type":21},"2025-10-01",{"date":134,"type":21},"2027-05-30",{"name":136,"class":44},"Chinese University of Hong Kong",2,{"id":139,"slug":140,"hasResults":11,"nctId":141,"briefTitle":142,"officialTitle":142,"acronym":4,"eligibilityCriteria":143,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":144,"enrollmentInfo":145,"targetDuration":4,"studyType":146,"phases":4,"briefSummary":147,"conditions":148,"keywords":152,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":157,"lastUpdatePostDateStruct":158,"startDateStruct":160,"completionDateStruct":162,"leadSponsor":164,"locationsCount":45},"100600769","distribution-of-mood-and-personality-characteristics-and-their-influence-on-treatment-compliance-100600769","NCT07101796","Distribution of Mood and Personality Characteristics and Their Influence on Treatment Compliance","Inclusion Criteria:\n\n* Age: 18\\~70 years old\n* Suspected OSA based on symptoms such as snoring, waking at night, daytime sleepiness, or requiring OSA screening due to related conditions; or confirmed OSA patients referred for sleep monitoring or CPAP pressure titration.\n* Subjects are conscious, utterly independent in behavioral and cognitive ability, and able to answer questions independently;\n* The patients gave informed consent to the study and cooperated with relevant treatment and evaluation.\n\nExclusion Criteria:\n\n* Age below 18 or above 70 years old\n* No symptoms suggestive of OSA and no need for OSA screening; or patients without confirmed OSA\n* lacking full independence in behavior and cognitive ability, unable to answer questions independently\n* Patients who did not give informed consent or were unwilling to cooperate with treatment and evaluation","70 Years",{"count":92,"type":21},"OBSERVATIONAL","This study intends to investigate the personality and psychological characteristics of OSA patients using classical standard scales and obtain treatment information and adherence data through prospective follow-up to summarize the distribution characteristics of mood and personality characteristics of OSA patients and their influence on treatment adherence. A thorough understanding of OSA patient characteristics from the perspective of personality and psychological characteristics will be of great significance to the classification of OSA patients, precision treatment, and improving treatment compliance.",[149,27,121,150,151],"Personality","Depression","Continuous Positive Airway Pressure (CPAP)",[153,154,155,121,156,151],"Obstructive sleep apnea","personality","patient compliance","depression","2025-07-28",{"date":159,"type":37},"2025-08-03",{"date":161,"type":37},"2024-09-14",{"date":163,"type":21},"2025-08",{"name":165,"class":44},"Peking University First Hospital",{"id":167,"slug":168,"hasResults":11,"nctId":169,"briefTitle":170,"officialTitle":171,"acronym":4,"eligibilityCriteria":172,"healthyVolunteers":89,"sex":16,"minAge":173,"maxAge":174,"enrollmentInfo":175,"targetDuration":4,"studyType":146,"phases":4,"briefSummary":177,"conditions":178,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":184,"lastUpdatePostDateStruct":185,"startDateStruct":187,"completionDateStruct":189,"leadSponsor":191,"locationsCount":45},"100521970","pain-clinic-provides-public-health-safety-100521970","NCT06076512","Pain Clinic Provides Public Health Safety","Pain Clinic Provides Public Health and Safety Services","Inclusion Criteria:\n\n* adult chronic pain patients\n* patients with psychosocial problems\n\nExclusion Criteria:\n\n* pediatric patients\n* patients with severe cognitive dysfunction","20 Years","99 Years",{"count":176,"type":21},1000,"Chronic pain is associated with psychological disorders; which may affect a patient's socioeconomic, legal, domestic, and employment situations. This prospective observational study evaluates the impact of pain management on patients' health, social, economic, and employment status. It explores the impact of pain clinic services on patients' mental health, family health, public health, road safety, addiction situation, public safety, injury rehabilitation and employment situation.",[179,180,181,182,27,183],"Social Functioning","Addiction, Substance","Safety Issues","Road Injury","Chronic Pain","2025-01-23",{"date":186,"type":37},"2025-01-27",{"date":188,"type":37},"2018-02-02",{"date":190,"type":21},"2025-12-31",{"name":192,"class":44},"Salem Anaesthesia Pain Clinic"]