Clinical trials: Consent of Patients
Prostatic Hyperplasia, Bladder Cancer
Information Improvement for Surgical Patients Through Portable Video Media
The aim of this study is to evaluate the comprehension of the Informed consent with the Standard Verbal Communication (SVC) versus Portable Video Media (PVM).
- Trial name
- NCT02846467
- Testing
- Informed consent trough a portable video media, Written informed consent
- Where
- Spain
- Volunteers
- 193 people
- Sponsor
- Hospital Universitario Puerto Real
Knee Osteoarthritis
The Age of OrthoInfo: A Randomized Controlled Trial Evaluating Patient Comprehension of Informed Consent
This study is a Non-funded, Single Center, Multi-Arm, Parallel Group Randomize Control Trial. In this study, the investigators aim to evaluate the impact of a visual aid on patient comprehension an orthopedic informed consent…
- Trial name
- NCT02416505
- Testing
- Verbal+Anatomic Model, Verbal+Video
- Volunteers
- 67 people
- Sponsor
- University of Missouri, Kansas City
Comprehension
Impact of Readability Improvements on the Comprehension of Written Information Given to Clinical Trial Patients: a RCT
The principle objective of this randomised controlled trial is to assess whether an improvement in lexico-syntactic readability combined with adherence to French recommendations for good practice in writing the Information and…
- Trial name
- LISYCOM (NCT00908557)
- Testing
- readability improvement and good practice redaction, Control
- Where
- France
- Volunteers
- 400 people
- Sponsor
- University Hospital, Grenoble
VR-based Informed Consent, Cataract and Intraocular Lens Surgery
VR for Cataract Anxiety Lowering Management
Cataract is currently the leading cause of blindness globally, and surgery is the only effective treatment. With the advancement of medical technology, cataract surgery is usually performed under topical anesthesia, which means…
- Trial name
- VR-CALM (NCT07586280)
- Testing
- Virtual reality simulation of intraoperative audiovisual experience
- Where
- China
- Volunteers
- 60 people
- Sponsor
- Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Arterial Line, Consent of Patients
Hemodynamic and Biological Evaluations During Reventilation Collapse in ICU
Prospective, observational clinical multicentric study in ICU; during the period surrounding the orotracheal intubation.
- Conditions
- Arterial Line, Consent of Patients, Adult Patients, Tracheal Intubation in ICU
- Trial name
- REVECOL (NCT01785654)
- Where
- France
- Volunteers
- 400 people
- Sponsor
- University Hospital, Clermont-Ferrand
Cancer
Health Literacy Intervention for Informed Consent of Cancer Patients Considering Clinical Trial Participation
This study will update an existing health literacy intervention (decision aid) for informed consent procedures and then conduct a randomized experiment implementing the health literacy intervention at Siteman Cancer Center and…
- Trial name
- NCT01964222
- Testing
- Decision Aid (DA)
- Where
- United States
- Volunteers
- 201 people
- Sponsor
- Washington University School of Medicine
Metastatic Pancreatic Cancer, Unresectable Pancreatic Cancer
EL CENTRO: Engaging Latinos in the Center of Cancer Treatment Options
The objective of this study is to improve the chemotherapy decision making process for Latinos with advanced gastrointestinal cancers.
- Conditions
- Metastatic Pancreatic Cancer, Unresectable Pancreatic Cancer, Metastatic Colorectal Cancer
- Trial name
- NCT03602885
- Testing
- Usual chemotherapy education (CE), Chemotherapy education intervention (CEI)
- Where
- 5 sites in United States
- Volunteers
- 10 people
- Sponsor
- Dana-Farber Cancer Institute
Brain Injuries
Study of NNZ-2566 in Patients With Traumatic Brain Injury Under EFIC
The purpose of this study is to determine whether NNZ-2566 is safe and effective in the treatment of Traumatic Brain Injury (TBI).
- Trial name
- INTREPID2566 (NCT01366820)
- Testing
- NNZ-2566
- Where
- 6 sites in United States
- Volunteers
- 261 people
- Sponsor
- Neuren Pharmaceuticals Limited
Solid Neoplasms
Improving Informed Consent for Early Phase Anti-Cancer Trials
The purpose of the trial will be to test whether providing both a short summary PIS and a link to a set of online video modules will improve patient understanding (those considering early phase clinical trials) as measured on the…
- Trial name
- CONSENT (NCT04407676)
- Testing
- Summary PIS and Online Video Modules
- Where
- United Kingdom
- Volunteers
- 34 people
- Sponsor
- Royal Marsden NHS Foundation Trust
Informed Consent, Awareness
Patients' Readings of Pre-operative Informed Consent Forms
Patient informed consent is a form which contains the patient's probable outcome of the procedure to be performed, and the probable risk and benefit of the patient's knowledge of the illness.
- Trial name
- NCT03555760
- Testing
- Observation of informed consent form readings of all patients who are scheduled for surgery
- Where
- Turkey (Türkiye)
- Volunteers
- 134 people, healthy volunteers welcome
- Sponsor
- Ankara University
Cognitive Decline, Cognitive Dysfunction
Open-label, Post-marketing, Prospective Study to Assess Impact of COVID-19 on Cognitive Function in Patients
The objective of this study is to compare the impact of the coronavirus disease (SARS-CoV-2, or COVID-19) on cognitive function in the population of patients who have been diagnosed, treated and recovered from the COVID-19…
- Conditions
- Cognitive Decline, Cognitive Dysfunction, Brain Health, Post CoV-2 Syndrome
- Trial name
- COVID19 (NCT04950673)
- Testing
- Cognivue
- Where
- 4 sites in United States
- Volunteers
- 1,000 people, healthy volunteers welcome
- Sponsor
- Cognivue, Inc.
Endometrium Cancer, Sentinel Lymph Node
Multimedia Aid Gynecologic Counseling and Consent
This is an interventional trial to introduce two short animated videos into preoperative counseling/consent and to compare patient comprehension and satisfaction with a multimedia approach compared to standard of care currently.
- Conditions
- Endometrium Cancer, Sentinel Lymph Node, Perioperative/Postoperative Complications
- Trial name
- NCT03899441
- Testing
- Video
- Where
- United States
- Volunteers
- 87 people, healthy volunteers welcome
- Sponsor
- UNC Lineberger Comprehensive Cancer Center
Knee Osteoarthritis
The Age of OrthoInfo: A Randomized Controlled Trial Evaluating Patient Comprehension of Informed Consent in a Private Practice
The aim of the study is determine which method of informed consent improves comprehension in college educated patients in a private practice setting.
- Trial name
- NCT02694237
- Testing
- Model, Knee Anatomy Video, Verbal
- Where
- United States
- Volunteers
- 66 people
- Sponsor
- University of Missouri, Kansas City
Critically Ill, Ethics
Barriers in the Process of Achieving Informed Consent From Critically Ill Patients
The study will explore barriers in the process of achieving informed consent from critically ill patients
- Conditions
- Critically Ill, Ethics, Informed Consent, Study Recruitment
- Trial name
- NCT03405766
- Where
- Norway
- Volunteers
- 70 people
- Sponsor
- Oslo University Hospital
Multiple Brain Metastases, Non-small-cell Lung Cancer
Phase Ⅲ Trial of WBRT Versus Erlotinib Concurrent Whole-brain Radiation Therapy as first-line Treatment for Patients With Multiple Brain Metastases From Non-small-cell Lung Cancer(ENTER): a Multicentre, Open-label, Randomised Study
1. Verify the effect of Erlotinib concurrent whole-brain radiation therapy as first-line treatment for patients with multiple brain metastases from non-small-cell lung cancer to compare with WBRT alone. 2.
- Trial name
- NCT01887795
- Testing
- Erlotinib, WBRT
- Where
- China
- Volunteers
- 224 people, healthy volunteers welcome
- Sponsor
- Daping Hospital and the Research Institute of Surgery of the Third Military Medical University
Distal Radius Fractures, Ankle Fractures
Improving Patient Understanding in Preoperative Informed Consent Process of Trauma Patients Using a Mixed Reality Viewer
This clinical trial aims to compare a Mixed Reality Viewer in the preoperative informed consent process to standard fracture visualization.
- Conditions
- Distal Radius Fractures, Ankle Fractures, Proximal Humeral Fracture
- Trial name
- NCT06062797
- Testing
- Mixed Reality Viewer, X-ray or CT scan
- Where
- Germany
- Volunteers
- 50 people
- Sponsor
- LMU Klinikum
Patient Education
Rapid Prototyping Models for Patient Education
Pre-made rapid prototyping models will be used to increase patient education versus current methodologies.
- Trial name
- NCT02718807
- Testing
- RP model explanation and questionnaire
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Milton S. Hershey Medical Center
Maternal Anxiety, Prenatal Diagnosis
Effect of Video -Based vs Standard ınformation on Maternal Anxiety and Procedure Decision in Pregnant Woman Offered Amniocentesis or Cvs
This prospective study evaluates the impact of video-based patient education compared to standard verbal informed consent on state anxiety levels and procedure acceptance rates in pregnant women undergoing invasive prenatal…
- Conditions
- Maternal Anxiety, Prenatal Diagnosis, Amniocentesis, Chorionic Villus Sampling
- Trial name
- NCT07876726
- Testing
- Multilingual Video-Based Patient Education, Standard Verbal Informed Consent
- Where
- Turkey (Türkiye)
- Volunteers
- 250 people, healthy volunteers welcome
- Sponsor
- Ankara City Hospital Bilkent
Psychosis
Enhancing Comprehension of Consent in Patients With Psychotic Disorders
: Informed consent is an important aspect of research, however in psychiatry research it remains an ethical dilemma, for the lack of clarity on the consent process deters some researchers from mental health research, and yet a…
- Trial name
- UBACC (NCT06975670)
- Testing
- multimedia consent tool
- Volunteers
- 60 people
- Sponsor
- Makerere University
Major Depressive Episode
Assessement of Capacity to Consent
Any patient can request euthanasia in many of our neighbouring European countries as long as informed consent is given. Psychiatric evaluation is not always mandatory.
- Trial name
- NCT04740463
- Where
- France
- Volunteers
- 70 people, healthy volunteers welcome
- Sponsor
- University Hospital, Montpellier