Risk Assessment

7

Review clinical trials related to Risk Assessment. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Adult Disease Risk Prediction Using Wearables, Hearing, and Health Data

This prospective cohort study aims to develop and validate a personalized disease risk prediction model for adults by integrating multiple sources of health data. The study will recruit community-dwelling adults aged 18 years and older in Taiwan. After providing informed consent, participants will complete a structured questionnaire, undergo pure tone hearing testing, and wear a smartwatch for 2 weeks to collect continuous physiological data, including heart rate and physical activity. With participant authorization, the study will also collect data from personal health records and national health insurance databases to allow longer-term follow-up of health outcomes. The main goals of the study are to examine the relationships among hearing, lifestyle factors, and wearable device data; to identify combinations of risk factors associated with progression from health to subclinical or chronic disease states; and to develop analytical methods for integrating heterogeneous health data from questionnaires, physiological monitoring, hearing tests, and medical databases. Machine learning methods will be used to identify important predictors and build risk prediction models. The study hypothesis is that combining hearing measures, lifestyle information, wearable physiological data, and longitudinal medical record data will improve the ability to identify individuals at higher risk of future disease compared with using a single source of information alone. The long-term objective is to support early risk identification, personalized health management, and prevention strategies in community adults.

Participants needed: 1,500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: National Health Research Institutes, TaiwanUpdated: Apr 21, 2026Locations: 1Duration: 2 Weeks
Eligibility criteria

Adults aged 18 years and older [+4]

Diagnosis of dementia [+3]

Status: Recruiting

Cardiac Magnetic Resonance-Clinical Prediction Model-Dilated Cardiomyopathy

Dilated cardiomyopathy (DCM) is a common and serious heart disease characterized by left ventricular enlargement and impaired pumping function, with adverse prognosis (including heart failure, arrhythmia, heart-related hospitalization, and death) being a major concern for patients. Currently, a critical gap exists in accurately predicting which DCM patients are at high risk of these severe outcomes, limiting targeted clinical care. This observational, non-invasive study aims to develop and validate a clinical prediction model for early risk warning of adverse prognosis in DCM patients. The model integrates multi-parameter stress perfusion cardiac magnetic resonance (MP stress perfusion CMR)-a safe, high-resolution imaging technique that assesses cardiac structure, function, blood perfusion, and tissue damage under mild stress-and standard clinical data (e.g., age, gender, blood pressure, and routine heart test results). The model will be trained and tested using follow-up data from hundreds of DCM patients, with the analysis identifying patterns in CMR and clinical data associated with adverse outcomes. Once validated for accuracy, the model will provide doctors with personalized risk scores to prioritize care for high-risk patients (e.g., early intervention, close monitoring) and avoid over-treatment for lower-risk individuals. Beyond clinical application, the study will enhance understanding of DCM progression, laying the groundwork for improved diagnostic tools, more effective treatments, and better strategies to prevent DCM-related complications, ultimately improving patient quality of life and reducing mortality.

Participants needed: 2,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Shandong Provincial HospitalUpdated: Apr 14, 2026Locations: 1Duration: 6 Months
Eligibility criteria

significant coronary artery disease (CAD), defined as a stenosis of ˃50% in a ma... [+4]

Status: Recruiting

Frailty and Muscle Strength Tests in Older Adults Undergoing Major Surgery

The goal of this observational study is to learn if simple tests for frailty and muscle strength can help predict which older adults (age 65 and older) are at higher risk for problems after major abdominal surgery. The main questions it aims to answer are: * Do measures of frailty and muscle strength, taken before surgery, predict complications after surgery? * Can these tests be easily done during a routine pre-surgical visit? Participants will: * Complete brief tests measuring muscle strength, breathing strength, physical function, nutrition status, body composition, and memory during a regular pre-surgical clinic appointment. * Allow researchers to review their medical records 30 and 90 days after surgery to identify any complications or health problems.

Participants needed: 100
Trial details
Age: 65+Biological sex: AllType: ObservationalSponsor: University of North Carolina, Chapel HillUpdated: Jan 28, 2026Locations: 1
Eligibility criteria

Age 65 years or older. [+3]

Surgery is an emergency procedure. [+2]

Status: Recruiting

Remote Monitoring of Asthma in Children and Young People

The objective of this study is to determine whether healthcare data and remotely collected patient data can accurately predict asthma attacks in children and young people aged 5-17 years. The main outcome is: when using this new system, is there a reduction in asthma attacks compared with a historic average. The whole population of children and young people with asthma will have routine healthcare data monitored, with a subset of people with high risk asthma asked to participate in a more detail study involving remotely monitored data.

Participants needed: 900
Trial details
Age: 5-17Biological sex: AllType: ObservationalSponsor: University of EdinburghUpdated: Jan 22, 2026Locations: 1
Eligibility criteria

Children and Young People with a diagnosis of asthma (coded as asthma or suspect...

Alternative non-asthma diagnosis that would require inhaled steroid [+3]

Status: Recruiting

Comparing CCI and POSSUM for Predicting Oncogynecologic Surgery Complications

With the global rates of gynecologic cancers on the rise, optimizing perioperative care is imperative. Accurate risk prediction is essential for enhancing patient care, directing preoperative interventions, and facilitating informed decision-making in oncology. This research compares two widely-used risk assessment tools: the Charlson Comorbidity Index (CCI) and the Physiological and Operative Severity Score for the enUmeration of Mortality and Morbidity (POSSUM), in predicting perioperative outcomes. The CCI predominantly addresses comorbidities, providing simplicity and broad applicability, while POSSUM incorporates both physiological and operative factors for a more comprehensive risk assessment. Despite their application across various surgical specialties, the specific utility of these tools in onco-gynecologic surgery remains insufficiently explored. The study aims to evaluate the effectiveness of CCI and POSSUM in predicting perioperative complications, with a focus on the incidence of these complications, length of hospital stay, and 30-day mortality. The implementation of these risk tools may enhance multidisciplinary risk management, thus improving patient outcomes in gynecologic oncology surgery.

Participants needed: 300
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Mahidol UniversityUpdated: Dec 17, 2025Locations: 1
Eligibility criteria

Age > 18 years [+1]

Patient required emergency surgery from any indication [+1]

Status: Recruiting

Risk Factors for Complications After Cranioplasty

Cranial defects often result from brain injuries, hemorrhages, strokes, or brain tumors. These conditions can increase pressure inside the skull, and if left untreated, may lead to dangerous complications like brain herniation. To manage this, a common procedure called decompressive craniectomy is performed to reduce intracranial pressure. While this surgery often stabilizes the patient's condition, it leaves a cranial defect that exposes the brain to external risks, including pressure fluctuations and potential damage. In severe cases, patients with larger defects may develop complications such as sinking skin flap syndrome. Cranial reconstruction, also known as cranioplasty, is an important procedure to restore the skull's structure and protect the brain. This surgery can improve brain function, stabilize intracranial pressure, and enhance the patient's appearance. While cranioplasty is a standard neurosurgical procedure, it has a relatively high risk of complications compared to other brain surgeries. Common complications include infections, bleeding, hydrocephalus, and seizures. In severe cases, complications may lead to the failure of the reconstruction. Understanding the factors that contribute to complications after cranioplasty is crucial for neurosurgeons to improve outcomes and reduce risks. This study aims to identify these factors and develop predictive models for postoperative complications of cranioplasty.

Participants needed: 1,000
Trial details
Biological sex: AllType: ObservationalSponsor: Qilu Hospital of Shandong UniversityUpdated: Jun 5, 2025Locations: 3
Eligibility criteria

Patients who underwent cranioplasty in the Department of Neurosurgery at Qilu Ho... [+3]

Patients with a prior history of cranioplasty [+3]

Status: Not yet recruiting

Preoperative Focused Cardiac Ultrasound in Hip Fracture Surgery (PrEcho)

The primary objective of this study is to investigate the impact of preoperative focused transthoracic ultrasound (FOCUS) on intraoperative hypotension and postoperative complications in hip fracture surgery. Our hypothesis is that a preoperative FOCUS along with a hemodynamic optimization protocol will reduce the occurrence of intraoperative drops in blood pressure and post-operative complications.

Participants needed: 100
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Umeå UniversityUpdated: Dec 8, 2023
Eligibility criteria

Patients ≥ 65 years of age, with American Socieity of Anesthesiologists (ASA) ph...

Metastatic cancer and/or suspect pathological fracture. [+4]