[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"nursing-interventions\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:nursing-interventions":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,52,81,117,147,182],{"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":34,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":51},"100631362","traction-pressure-and-rapid-muscle-release-tpr-technique-during-intramuscular-injection-effects-on-pain-and-patient-satisfaction-100631362",false,"NCT07499687","Traction, Pressure, and Rapid Muscle Release (TPR) Technique During Intramuscular Injection: Effects on Pain and Patient Satisfaction","The Effect of the Traction, Pressure, and Rapid Muscle Release (TPR) Technique on Pain and PatientSatisfaction During Intramuscular Injection: A Randomized Controlled Experimental Study","TPRTDIMI","Inclusion Criteria:\n\n* Voluntary participation in the study\n* Ability to speak and understand Turkish\n* Being between 18 and 65 years of age\n* Having a body mass index (BMI) between 18.5 and 30\n* No sensory impairment in the ventrogluteal muscles\n\nExclusion Criteria:\n\n* Presence of a scar, burn, redness, hematoma, bruising, tenderness, or induration at the injection site\n* History of intramuscular injection in the ventrogluteal region within the last 15 days\n* Presence of injection-related fear\n* Diagnosis of Diabetes Mellitus\n* History of neuropathy\n* Presence of any hearing, visual, or speech impairment\n* Presence of a mental disability\n* Use of oral or parenteral analgesic medication before the procedure.",true,"ALL","18 Years","65 Years",{"count":22,"type":23},102,"ESTIMATED","INTERVENTIONAL",[26],"NA","This study will be conducted to evaluate the effect of the Traction, Pressure, and Rapid Muscle Release (TPR) technique, an innovative method used during intramuscular vitamin B12 (cyanocobalamin) injections, on patients' pain and satisfaction levels compared with the conventional injection method.",[29,30,31,32,33],"Injection Techniques","Nursing Interventions","Injection Pain Prevention","Patient Satisfaction","Intramuscular Injection",[35,36,37,38],"intramuscular injection","tpr technique","pain","satisfaction","NOT_YET_RECRUITING","2026-03-24",{"date":42,"type":43},"2026-03-30","ACTUAL",{"date":45,"type":23},"2026-04-06",{"date":47,"type":23},"2026-10",{"name":49,"class":50},"Bezmialem Vakif University","OTHER",1,{"id":53,"slug":54,"hasResults":11,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":4,"eligibilityCriteria":58,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":59,"targetDuration":4,"studyType":24,"phases":61,"briefSummary":62,"conditions":63,"keywords":66,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":4},"100622570","comfort-communication-model-intervention-for-burn-pain-and-pain-anxiety-100622570","NCT07385339","Comfort Communication Model Intervention for Burn Pain and Pain Anxiety","The Effect of a Nursing Intervention Based on the Comfort Communication Model on Pain and Pain Anxiety in Outpatient Burn Patients: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Be 18 years of age or older,\n* Patients with at least three dressing experiences\n* Patients with 2nd and 3rd degree burns\n* No difficulty communicating in Turkish,\n* No hearing problems or cognitive impairment,\n* No additional mental disorders,\n* Willingness to cooperate,\n* No additional mental disorders,\n* Ability to perform self-care,\n* Patients who voluntarily agreed to participate in the study\n\nExclusion Criteria:\n\n* First-time burn care dressing\n* Having a first-degree burn\n* Actively receiving inpatient treatment\n* Having a neurological or psychiatric condition that prevents reading and understanding data collection tools\n* Having difficulty speaking\u002Funderstanding Turkish",{"count":60,"type":23},62,[26],"This single-center, randomized controlled trial will evaluate the effect of a nursing intervention based on the COMFORT Communication Model on procedural pain and burn-specific pain anxiety in adult outpatient burn patients undergoing routine dressing changes at the Adult Burn Center Outpatient Unit of Ankara Bilkent City Hospital. Burn dressing changes are frequently perceived as one of the most painful non-surgical procedures, and repeated exposure to wound care may contribute to anticipatory anxiety and stress, potentially creating a reinforcing cycle in which anxiety amplifies pain and pain increases anxiety. In outpatient burn care, effective nurse-patient communication may play a critical role in improving comfort, supporting coping, and enhancing engagement in ongoing treatment.\n\nEligible participants will be adults aged 18 years and older with second- or third-degree burns who have experienced at least three prior dressing changes, can communicate in Turkish, and have no major hearing or cognitive impairment or comorbid psychiatric\u002Fneurological condition that would prevent understanding of the study procedures. Participants who request withdrawal, require hospitalization during follow-up, or miss two consecutive intervention sessions will be withdrawn from the study. The required minimum sample size was estimated as 62 patients (31 per group) based on power analysis (effect size f=0.30; 80% power).\n\nAfter providing written and verbal informed consent, participants will be randomly assigned (simple randomization using Random Allocation Software) to either the COMFORT-based communication intervention group or the usual care control group. Data will be collected face-to-face in a quiet and private environment during dressing visits. At the initial visit, participants in both groups will complete a sociodemographic and burn-related information form and baseline assessments. Pain intensity will be evaluated using a Verbal Rating Scale and a Numeric Rating Scale, and pain anxiety will be assessed using the Burn-Specific Pain Anxiety Scale; perceived stress will also be measured.\n\nThe intervention will be delivered by a wound care nurse during three consecutive dressing sessions. Each session is structured to last approximately 10 minutes and uses specific components of the COMFORT Communication Model tailored to the dressing-change context. In Session 1, the focus is on establishing trust, providing clear information, and supporting patient control through Connection\u002FCommunication, Orientation and opportunity, and Relating strategies (e.g., explaining the procedure step-by-step, checking understanding, offering supportive options, and inviting the patient to signal if they want pauses). In Session 2, the focus shifts to creating space for emotions and strengthening supportive openings using Mindful communication, Openings, and Family components (e.g., exploring how the prior session felt, inviting expression of concerns, and identifying supportive persons). In Session 3, communication emphasizes personalization, meaning-making, and teamwork by integrating Relating, Team, and Meaning-focused prompts (e.g., reflecting on what was most helpful, supporting adaptive coping, and, if appropriate, facilitating communication with the clinical team). Throughout all sessions, routine wound care will continue as standard practice in both groups.\n\nOutcomes will be assessed repeatedly across the three dressing sessions. Pain and pain anxiety will be assessed before each dressing, and follow-up assessments will be repeated approximately 30 minutes after the dressing procedure. The primary objective is to determine whether COMFORT model-based nursing communication reduces procedural pain intensity and burn-specific pain anxiety compared with usual care during outpatient dressing changes. A secondary objective is to evaluate whether the intervention reduces perceived stress across sessions. Statistical analyses will include appropriate descriptive and repeated-measures comparisons to examine group differences over time.",[64,65,30],"Burn Patients","Pain Management",[67,68,37,69,70,71],"burn patients","dressing change","pain anxiety","Comfort communication model","nursing intervention","2026-02-27",{"date":74,"type":43},"2026-03-02",{"date":76,"type":23},"2026-02-17",{"date":78,"type":23},"2026-06-10",{"name":80,"class":50},"Baskent University",{"id":82,"slug":83,"hasResults":11,"nctId":84,"briefTitle":85,"officialTitle":86,"acronym":4,"eligibilityCriteria":87,"healthyVolunteers":11,"sex":18,"minAge":88,"maxAge":4,"enrollmentInfo":89,"targetDuration":4,"studyType":24,"phases":91,"briefSummary":92,"conditions":93,"keywords":98,"overallStatus":106,"whyStopped":4,"lastUpdateSubmitDate":107,"lastUpdatePostDateStruct":108,"startDateStruct":110,"completionDateStruct":112,"leadSponsor":114,"locationsCount":51},"100623756","hope-theory-based-nursing-intervention-after-hip-fracture-surgery-100623756","NCT07400770","Hope Theory-Based Nursing Intervention After Hip Fracture Surgery","Effect of a Snyder Hope Theory-Based Nursing Intervention on Psychological Status, Pain, and Functional Recovery in Elderly Patients After Hip Fracture Surgery: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Age ≥ 60 years.\n* Patients with hip fracture requiring surgical intervention.\n* Patients who have undergone hip fracture surgery within the past 2 weeks.\n* Patients who are able to communicate and provide informed consent.\n* Patients and\u002For their family members who are willing to participate in the study.\n\nExclusion Criteria:\n\n* Patients with other lower limb fractures or history of lower limb thrombosis.\n* Patients with multiple fractures.\n* Patients with severe damage to major organs (heart, lungs, brain) or malignant tumors.\n* Patients who have undergone hip replacement surgery in the past.\n* Patients with infectious diseases or immune system disorders.\n* Patients with chronic diseases or neurological disorders.","60 Years",{"count":90,"type":23},112,[26],"This is a randomized controlled trial to evaluate the effectiveness of a Snyder Hope Theory-based nursing intervention on elderly patients following hip fracture surgery. The study aims to improve the patient's psychological well-being, reduce pain, and enhance their functional recovery. Participants will be randomly assigned to either the intervention group or the control group. The intervention involves individualized counseling, goal setting, and rehabilitation training based on the Snyder Hope Theory. The trial will assess changes in hope levels, anxiety, pain, hip joint function, and quality of life before and after the intervention.",[94,95,96,30,97],"Hip Fracture","Elderly Patients","Postoperative Recovery","Snyder Hope Theory",[99,100,101,102,103,104,105],"Hope Theory","Elderly Hip Fracture Surgery","Postoperative Nursing","Psychological Counseling","Rehabilitation Training","Pain Management, Anxiety","Quality of Life","RECRUITING","2026-02-03",{"date":109,"type":43},"2026-02-10",{"date":111,"type":43},"2024-05-01",{"date":113,"type":23},"2026-11-30",{"name":115,"class":116},"Institute of Orthopaedic Surgery, Taizhou No.3 People's Hospital","OTHER_GOV",{"id":118,"slug":119,"hasResults":11,"nctId":120,"briefTitle":121,"officialTitle":122,"acronym":4,"eligibilityCriteria":123,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":124,"targetDuration":4,"studyType":24,"phases":125,"briefSummary":126,"conditions":127,"keywords":131,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":138,"lastUpdatePostDateStruct":139,"startDateStruct":141,"completionDateStruct":143,"leadSponsor":145,"locationsCount":51},"100602646","hot-water-foot-bath-for-pain-and-gas-relief-after-laparoscopic-cholecystectomy-100602646","NCT07126223","Hot Water Foot Bath for Pain and Gas Relief After Laparoscopic Cholecystectomy","The Effect of Hot Water Foot Bath on Pain and Gas Release After Laparoscopic Cholecystectomy: A Randomised Controlled Trial","Inclusion Criteria:\n\n* Age 18 years or older\n* Undergoing elective laparoscopic cholecystectomy\n* Received the same preoperative gastrointestinal preparation protocol\n* Received the same postoperative analgesia protocol\n* Numeric Rating Scale (NRS) pain score of 3 or higher at the 3rd postoperative hour\n* Voluntarily agreed to participate and signed the informed consent form\n* Classified as ASA I or ASA II according to the American Society of Anesthesiologists (ASA)\n\nExclusion Criteria:\n\n* Undergoing emergency cholecystectomy or open surgery (laparotomy)\n* Presence of open wounds, infections, circulatory disorders, or lesions in the feet (hot foot bath area)\n* Use of patient-controlled analgesia (PCA) in the early postoperative period\n* Any condition that impairs verbal communication\n* History of inflammatory bowel disease (due to potential influence on bowel motility)\n* Use of medications or probiotic agents affecting bowel motility in the pre- or postoperative period",{"count":60,"type":23},[26],"This study investigates the effects of a hot foot bath on postoperative pain and time to first gas release in patients undergoing laparoscopic cholecystectomy. The intervention is a non-pharmacological supportive method applied during the early postoperative period. Participants will be randomly assigned to either intervention or control groups. No FDA-regulated drug or device is involved.",[128,129,130,96,30],"Laparoscopic Cholecystectomy","Postoperative Pain","Gastrointestinal Motility",[132,133,134,135,136,137],"foot bath","gas release","pain management","complementary therapy","nursing","cholesistectomy","2025-12-04",{"date":140,"type":43},"2025-12-05",{"date":142,"type":23},"2025-12-20",{"date":144,"type":23},"2026-06-30",{"name":146,"class":50},"Cansu Mert",{"id":148,"slug":149,"hasResults":11,"nctId":150,"briefTitle":151,"officialTitle":152,"acronym":153,"eligibilityCriteria":154,"healthyVolunteers":11,"sex":18,"minAge":155,"maxAge":156,"enrollmentInfo":157,"targetDuration":4,"studyType":24,"phases":159,"briefSummary":160,"conditions":161,"keywords":166,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":173,"lastUpdatePostDateStruct":174,"startDateStruct":176,"completionDateStruct":178,"leadSponsor":180,"locationsCount":51},"100612359","mouthwash-temperature-and-oral-mucositis-in-head-and-neck-radiotherapy-100612359","NCT07252557","Mouthwash Temperature and Oral Mucositis in Head and Neck Radiotherapy","Effectiveness of Different Mouthwash Temperatures on Oral Mucositis Pain and Patient Comfort During Radiotherapy for Head and Neck Cancer: A Randomized Controlled Trial","CoolRinseHNC","Inclusion Criteria:\n\n* Histologically confirmed head and neck cancer (HNC) receiving radiotherapy for the first time, with or without concurrent chemotherapy.\n* Conscious, communicative, and able to perform the rinsing procedure and complete questionnaires.\n* Provided written informed consent prior to enrollment.\n\nExclusion Criteria:\n\n* Non-HNC diagnoses or radiotherapy to sites outside the oral\u002Foropharyngeal region.\n* Cognitive impairment or inability to complete the rinsing protocol.","20 Years","80 Years",{"count":158,"type":23},200,[26],"This single-center randomized controlled trial evaluates the effects of cold (15-20°C) versus room-temperature (30-35°C) water gargling on oral mucositis severity, pain, and comfort in patients with head and neck cancer undergoing radiotherapy. Participants will rinse their mouth four times daily for 30-60 seconds over a 6-week radiotherapy course, with follow-up for two additional weeks. The study hypothesizes that cold-water rinsing can reduce the severity of radiation-induced oral mucositis (RTOM) and pain, improve oral comfort, and minimize treatment interruptions.",[162,163,164,30,165],"Head and Neck Cancer (H&Amp;Amp;N)","Radiation-induced Oral Mucositis","Supportive Care","Radiotherapy Side Effects",[167,168,169,170,164,65,171,172],"Head and Neck Cancer","Radiation-Induced Oral Mucositis","Water Temperature","Cold Water Rinse","Radiotherapy","Nursing Intervention","2025-11-24",{"date":175,"type":43},"2025-11-26",{"date":177,"type":23},"2026-01-01",{"date":179,"type":23},"2027-03-31",{"name":181,"class":50},"Chung Shan Medical University",{"id":183,"slug":184,"hasResults":11,"nctId":185,"briefTitle":186,"officialTitle":187,"acronym":4,"eligibilityCriteria":188,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":189,"targetDuration":4,"studyType":24,"phases":191,"briefSummary":192,"conditions":193,"keywords":4,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":199,"lastUpdatePostDateStruct":200,"startDateStruct":202,"completionDateStruct":204,"leadSponsor":206,"locationsCount":4},"100604118","virtual-reality-intervention-for-symptom-management-in-stem-cell-transplantation-100604118","NCT07145359","Virtual Reality Intervention for Symptom Management in Stem Cell Transplantation","Development and Evaluation of A Virtual Reality Intervention for Symptoms Management During Hematopoietic Stem Cell Transplantation","Inclusion Criteria:\n\n* Patients aged 18 years or older\n* Able to speak and understand Turkish\n* Scheduled to undergo allogeneic hematopoietic stem cell transplantation (HSCT)\n* Receiving stem cell products collected from peripheral blood\n* Voluntarily agree to participate in the study and provide informed consent\n\nExclusion Criteria:\n\n* Undergoing autologous hematopoietic stem cell transplantation\n* Receiving stem cell products collected from bone marrow\n* Diagnosed with medical or psychiatric comorbidities that could interfere with participation, as reported by the healthcare team\n* Presenting infection symptoms (e.g., respiratory, gastrointestinal) that may contaminate study equipment, as identified by the healthcare team\n* Having visual, auditory, verbal, or cognitive impairments that may prevent interaction with the VR equipment\n* Previously received any form of hematopoietic stem cell transplantation",{"count":190,"type":23},30,[26],"The goal of this clinical trial is to evaluate whether a virtual reality (VR) intervention based on the Symptom Management Model can reduce physical and psychosocial symptoms during hematopoietic stem cell transplantation (HSCT) in adult patients undergoing allogeneic transplantation.\n\nThe main questions it aims to answer are:\n\nDoes the VR intervention reduce distress levels during HSCT?\n\nDoes the VR intervention decrease state anxiety and symptom severity compared to standard care?\n\nDoes the VR intervention positively affect physiological outcomes and engraftment times?\n\nResearchers will compare a group receiving standard clinical care plus a VR nature-themed video during HSCT to a group receiving standard care only to see if the VR intervention improves symptom management outcomes.\n\nParticipants will:\n\nBe randomly assigned to either the intervention or control group.\n\nIn the intervention group:\n\nWatch a 15-minute nature-themed VR video during stem cell infusion using Meta Quest 3.\n\nThe video content will be specifically created by the research team based on the principles of Attention Restoration Theory (ART).\n\nIn both groups:\n\nComplete pre- and post-intervention assessments including:\n\nDistress Thermometer\n\nState-Trait Anxiety Inventory\n\nEdmonton Symptom Assessment Scale\n\nPhysiological measures (vital signs)\n\nEngraftment tracking\n\nSatisfaction and open-ended feedback forms",[194,195,30,196,197,198],"Cancer and \u002F or Hematological Malignancy","Hematopoetic Stem Cell Transplantation","Symptom Management","Virtual Reality","ALLOGENEIC HEMATOPOIETIC STEM CELL TRANSPLANTATION","2025-08-21",{"date":201,"type":43},"2025-08-28",{"date":203,"type":23},"2025-09-10",{"date":205,"type":23},"2026-09-10",{"name":207,"class":50},"Halic University"]