Educational Problems

13

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

Condition / disease
Location
Status: Recruiting

Health Equity and Rural Education (HERE!) Clinical Trial

The goal of this community-engaged research is two-fold. The first goal is to gather stakeholder feedback to inform a school-based community health worker intervention with youth with poor school attendance and an enhanced usual care condition. The second goal is to evaluate the feasibility of implementing the school-based community health worker intervention and enhanced usual care approach within rural schools. The main question it aims to answer is whether it is feasibile to recruit children with poor school attendance and their families to the intervention, to complete the trauma-informed intervention, and to complete the associated study measures of meeting social determinants of health/mental health needs, school-based health center utilization, and behavioral helath symptoms. At least 38 rural students in grades 6-12 with poor school attendance and their parents/guardians will meet with the school-based community health worker for support around social determinants of health needs that may be barriers to attendance. Researchers will also assess the feasibility of recruiting at least 10 rural students and their parents/guardians to complete the study measures in an enhanced usual care condition in which the school-based health center without a school-based community health worker is reminded of the availability of an online social services directory.

Participants needed: 126
Trial details
Age: 12+Biological sex: AllType: InterventionalSponsor: University of Kansas Medical CenterUpdated: Apr 20, 2026Locations: 1
Eligibility criteria

A member of the program's Community Advisory Board, including community health w... [+4]

Parents/guardians or youth with profound intellectual/cognitive disability will...

Status: Not yet recruiting

Nurse vs Physician Artery Cannulation

This prospective controlled clinical trial evaluates the effectiveness and safety of radial artery cannulation using the Seldinger technique under ultrasound guidance when performed by two different operator groups: experienced physicians and trained registered nurses. The study aims to determine whether a structured, competency-based training program enables nurses without prior experience in arterial cannulation to achieve comparable outcomes to physicians in terms of first-attempt success rate, procedural efficiency, and complication rates.

Participants needed: 560
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Masarykova Nemocnice v Usti nad Labem, Krajska Zdravotni a.s.Updated: Mar 31, 2026
Eligibility criteria

Nurse with successful completion of the predefined radial artery catheterization... [+1]

Absence of competency for radial artery catheterization.

Status: Not yet recruiting

Point-of-Care Ultrasound (PoCUS) Teleeducation Curriculum for Hospital-at-home Care

Since July 2024, the National Health Insurance Administration (NHIA) has been implementing a pilot Hospital-at-Home (HAH) Acute Care Program to curb hospital admissions. Point-of-Care Ultrasound (PoCUS) is considered the most promising imaging tool for this model. Replicating the hospital's familiar environment-its staffing patterns, diagnostic workflows, and medication protocols-in a patient's home or nursing facility is almost impossible, posing a major challenge to care teams. Medical-simulation training offers a solution, yet current PoCUS courses remain organ-based and lack scenario-based simulations that prepare physicians for HAH practice. This two-year study will create a PoCUS curriculum and outcome-assessment tools tailored to HAH, adapting previously validated Entrustable Professional Activities (EPA) instruments to three HAH scenarios: pneumonia, urinary tract infection, and soft-tissue infection. Year 1 will develop scenario-based simulation courses and matching EPA tools, and train peer instructors who receive full PoCUS instruction for the three scenarios. Year 2 will randomly assign learners to compare two teaching models-peer training with remote supervision and scenario simulation versus traditional PoCUS training-evaluated with an Objective Structured Clinical Examination (OSCE) scored by EPA forms across multiple domains. The project aims to establish normative standards for PoCUS training and assessment in HAH, confirm the feasibility of peer training with remote supervision, and provide a platform to train HAH medical teams nationwide, including those in rural areas.

Participants needed: 100
Trial details
Age: 20+Biological sex: AllType: InterventionalSponsor: National Taiwan University HospitalUpdated: Dec 17, 2025Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Off-script Diagnosis & Differential Diagnosis (D&D) Training and Residents' Stroke Knowledge

This study is a single-center, randomized, open-label, controlled, endpoint-blinded study to assess the effect of off-script diagnosis \& differential diagnosis (D\&D) training in improving the residents' knowledge of acute ischemic stroke in China. The investigators will enroll 22 residents and assess the score of mASMaQ 30 days after randomization.

Participants needed: 22
Trial details
Biological sex: AllType: InterventionalSponsor: Peking Union Medical College HospitalUpdated: Jun 26, 2025Locations: 1
Eligibility criteria

Residents (physicians in postgraduate training). [+3]

Managing asymptomatic ischemic stroke patients. [+1]

Status: Recruiting

3D Resin Printed Fracture Models for Anatomy Education

Resin printing is an emerging technology with a wide array of applications. This research seeks to assess the practicality of incorporating 3D resin printed models into anatomy education while investigating how fractured models impact students' decision-making and quiz scores.

Participants needed: 98
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Abant Izzet Baysal UniversityUpdated: May 28, 2025Locations: 1
Eligibility criteria

having stereopsis above 40 arc/seconds according to the Titmus Stereopsis Test

having partial or total vision loss [+2]

Status: Not yet recruiting

Standardized Educational Videos of Laparoscopic Gynecological Surgeries

Owing to coronavirus disease-related social distancing requirements, online education has gained prominence. Surgical trainers consider online videos as a useful teaching aid that maximizes trainees' learning and skill development given the backdrop of time constraints and productivity demands, however, online videos usually do not undergo a peer-review process. Based on these premises the LAP-VEGaS guidelines (LAParoscopic surgery Video Educational GuidelineS), a recommended checklist for production of educational surgical videos, were developed. This study aime to evaluate the impact of educational videos of laparoscopic gynecological surgeries, that were standardized with the LAP-VEGaS, for the improvement of surgical confidence and performance of surgical trainees.

Participants needed: 50
Trial details
Biological sex: AllType: InterventionalSponsor: The University of Texas Health Science Center, HoustonUpdated: Apr 10, 2025
Eligibility criteria

Not listed

Status: Recruiting

The Effect of Mandala Coloring Activity on Test Anxiety

This study aims to investigate the effect of mandala coloring activity on test anxiety of nursing students.

Participants needed: 62
Trial details
Biological sex: AllType: InterventionalSponsor: Nursemin ÜNALUpdated: Feb 28, 2025Locations: 1
Eligibility criteria

Being a student enrolled in the Mental Health and Psychiatric Nursing course at... [+3]

Students with psychological diagnoses such as anxiety or depression. [+2]

Status: Recruiting

Impact of Virtual Reality Model for Pelvic Floor Anatomy on Users' Educational Level and Experience

The purpose of the study is to evaluate the impact of virtual reality (VR) model for pelvic floor anatomy on users' educational level and experience.

Participants needed: 50
Trial details
Age: 19-45Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Feb 25, 2025Locations: 1
Eligibility criteria

Physical therapy undergraduate, graduate, and postgraduate students, as well as... [+1]

Lack of Anatomy Background. [+2]

Status: Recruiting

The Holographic Standardized Patient

The current pandemic has revealed in-person simulation training and evaluation is vulnerable to disruption, and alternatives are needed which allow remote evaluation. The recently developed Microsoft Hololens headset device allows interactable holograms to be inserted into a user's workspace (mixed reality) - permitting the augmentation of existing clinical and training spaces with holographic (i.e. virtual) patients via the prototype HoloSIM software. This study is the first known research initiative aiming to demonstrate the feasibility and effectiveness of mixed reality for acute medicine training and assessment at a distance. Space, time, personnel, pandemic, and cost constraints limit opportunities for high-fidelity simulation exercises for post-graduate trainees at Sunnybrook. By developing and demonstrating the effectiveness of this new training modality, increased simulation exercises will lead to a higher quality education experience, better functioning teams, and better patient outcomes.

Participants needed: 40
Trial details
Age: 20-100Biological sex: AllType: InterventionalSponsor: Sunnybrook Health Sciences CentreUpdated: Jan 29, 2025Locations: 1
Eligibility criteria

Resident or fellow level volunteers from acute care postgraduate training progra...

Unwilling to enter the study [+1]

Status: Recruiting

Evaluation of the Dental Educational Environment Using the DREEM Tool

This Cross-Sectional Study aims to evaluate the dental educational environment in Upper Egypt using the Dundee Ready Education Environment Measure (DREEM) Questionnaire.

Participants needed: 215
Trial details
Biological sex: AllType: ObservationalSponsor: Beni-Suef UniversityUpdated: Jan 17, 2025Locations: 1Duration: 1 Day
Eligibility criteria

Students registered in the Faculty of Dentistry, Beni-Suef University

Status: Recruiting

Teaching Electronic Fetal Monitoring to Midwifery Students With Peer Teaching Method

706 / 5.000 The aim of the study is to examine the effects of Electronic Fetal Monitoring (EFM) (a test that evaluates fetal health during pregnancy) training given to midwifery students through peer education method on the knowledge, skills and self-efficacy levels of the students. It is being conducted as an experimental study with a randomized controlled pre-test-post-test design. Students were given standard training on EFM. Students in the peer teaching group were given peer education. Students continue to be evaluated while applying EFM to pregnant women in clinical practice. Personal information form, achievement test for EFM, skill form and Electronic Fetal Monitoring Self-Efficacy Scale were used in the evaluation of the students.

Participants needed: 72
Trial details
Biological sex: AllType: InterventionalSponsor: Tokat Gaziosmanpasa UniversityUpdated: Jan 14, 2025Locations: 1
Eligibility criteria

volunteers to participate in the study, [+3]

Students who are absent on the day the EFM topic is taught.

Status: Not yet recruiting

The Effect of Touchpoint Method on Clinical Learning; Experience With Nursing Students

This research aims to evaluate the effect of Touchpoint experience as a clinical learning method on clinical learning. The research is a quasi-experimental research with experimental-control groups. Students will be divided into experimental and control groups with the "simple randomization" method. A pre-test will be taken with data collection tools before the study for both groups. Students in the control group will continue their routine practice experiences. A post-test will be applied with data collection tools at the end of the 8-week internship period. TouchPoint is planned as a 2-session experience over a semester: Session 1 focuses on patient-centered care, Session 2 focuses on teamwork and collaboration. The method of both sessions will be conducted by 2 researchers with a small clinical group of 8 to 10 students. Sessions will last from 1.5 hours to 2 hours depending on the number of students and the degree of discussion. Sessions will be conducted face-to-face in a classroom.

Participants needed: 290
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Ataturk UniversityUpdated: Oct 21, 2024
Eligibility criteria

Being a 2nd year student at the Faculty of Nursing, [+1]

Not being a 2nd year student at the Faculty of Nursing, [+1]

Status: Recruiting

Multimodal Program for Cancer Related Cachexia Prevention

The aim of the study is to evaluate the effectiveness of a multifactorial education and support program for the prevention of cancer-related cachexia syndrome, for patients and their family caregivers during anti-cancer treatment.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Cyprus University of TechnologyUpdated: Sep 2, 2022Locations: 1
Eligibility criteria

18 years old or older [+4]

Haematologic tumors [+7]