Clinical trials: Consent Forms
Scleroderma
Empirical Comparative Study of Variation Blood Level Antibody Vitamin D at Scleroderma (SSc) Patients Compared Healthy Peoples
The aim is to find the presence of anti vitamin D antibodies in scleroderma patients and compare with control. A second goal is anti vitamin D levels in serum of scleroderma patients in relation to the clinical manifestations of…
- Trial name
- SSc (NCT01553890)
- Testing
- Blood sample
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Meir Medical Center
Informed Consent, Comprehension
AI-Driven Consent Simplification Study
The overarching goal of this pilot is to explore how generative artificial intelligence (genAI) can be used to improve the accessibility and understandability of informed consent materials in clinical research.
- Conditions
- Informed Consent, Comprehension, Communication, Disclosure
- Trial name
- ACCESS (NCT07303517)
- Testing
- Original ICF, AI Simplified ICF, Podcast - Original ICF
- Where
- United States
- Volunteers
- 226 people, healthy volunteers welcome
- Sponsor
- University of California, Los Angeles
Consent Forms, Asthma
Informed Consent Formats by Information Preference and Priority
This study will test whether different formats of medical informed consent documents can help improve understanding and confidence in decision-making for clinical trials. The study will be primarily run through an online survey.
- Trial name
- NCT03416907
- Testing
- Original consent form, Shortened consent form, Reordered, shortened consent form
- Where
- United States
- Volunteers
- 500 people, healthy volunteers welcome
- Sponsor
- Carnegie Mellon University
Lumbar Radiculopathy
Comparison Between the Imaging Consent Form and the Existing Narrative Consent Form
This is a single-center, randomized, double-blind clinical study to compare patient comprehension and anxiety by comparing a traditional paper consent form to a multimedia consent form for patients undergoing transforaminal…
- Trial name
- NCT05874427
- Testing
- Multimedia informed consent, Standard informed consent
- Where
- South Korea
- Volunteers
- 34 people, healthy volunteers welcome
- Sponsor
- Seoul National University Hospital
Attitude to Computers, Attitude of Health Personnel
An Interactive Patient-Centered Consent for Research Using Medical Records
The goal of this project is to develop and evaluate a novel, electronic informed consent application for research involving electronic health record (EHR) data.
- Conditions
- Attitude to Computers, Attitude of Health Personnel, Researcher-Subject Relations, Trust
- Trial name
- NCT03063268
- Testing
- Trust-Enhanced Messaging on E-Consent, Interactive features on E-Consent, Standard E-Consent
- Where
- United States
- Volunteers
- 734 people, healthy volunteers welcome
- Sponsor
- University of Florida
Early Detection of Cancer
Evidence-informed Choice for Women Participating in Mammography Screening
Study objectives: to evaluate the effects of information about benefits and risks of mammography screening on participants in terms of knowledge, attitude, rates of uptake, fear of cancer, anxiety, and conflict decision.
- Trial name
- NCT01335906
- Testing
- Information
- Where
- Spain
- Volunteers
- 332 people, healthy volunteers welcome
- Sponsor
- Andaluz Health Service
Outcome Assessments (Health Care), Comprehension
Evaluation of Readability of Consent Forms on the Understanding of the Information Received by Volunteers
Prior to the completion of biomedical research, any person undergoing it must receive a readable and intelligible information about this research, in order to give free and informed consent.
- Conditions
- Outcome Assessments (Health Care), Comprehension, Language
- Trial name
- NCT03105752
- Testing
- Questionnaire of understanding
- Volunteers
- 240 people, healthy volunteers welcome
- Sponsor
- Groupe Hospitalier Pitie-Salpetriere
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.
Adolescent Behavior
Simplified Consent for HIV Vaccine Trials
The main goal of this project is to develop and evaluate a simplified version of an HIV vaccine trial consent form designed for high-risk adolescents.
- Trial name
- NCT00105339
- Where
- 3 sites in United States
- Volunteers
- 255 people, healthy volunteers welcome
- Sponsor
- University of North Carolina, Chapel Hill
Sleep Disorders
Circadian Regulation of Sleep in Habitual Short Sleepers and Long Sleepers
Routine sleep duration varies greatly among individuals. The biological meaning of this variation is unknown. The term circadian rhythm refers to the biological clock that regulates the timing of falling asleep, waking up, and…
- Trial name
- NCT00001546
- Where
- United States
- Volunteers
- 38 people, healthy volunteers welcome
- Sponsor
- National Institute of Mental Health (NIMH)
Age 3 to 16 Years (Inclusive), Male or Female, Clinical Diagnosis Confirming That Myopia Has Occurred in at Least One Eye
The Effectiveness and Safety of Low-intensity Single-wavelength Red Light in Controlling High Myopia in Children and Adolescents：A Randomized, Controlled, Multicenter Clinical Trial
Objective: To study the effectiveness and safety of low-intensity single wavelength red light in controlling high myopia in children and adolescents. Methods: Subject population: Children aged 3-16 years who have high myopia.
- Conditions
- Age 3 to 16 Years (Inclusive), Male or Female, Clinical Diagnosis Confirming That Myopia Has Occurred in at Least One Eye, The Guardian Voluntarily Signed the Subject's Informed Consent Form
- Trial name
- NCT05184621
- Testing
- Eyesing Redlight Instrument
- Where
- China
- Volunteers
- 192 people, healthy volunteers welcome
- Sponsor
- Shanghai Eye Disease Prevention and Treatment Center
Alzheimer Disease, Early Onset, Mild Cognitive Impairment
Engagement 2.0 Forms of Consent for Data (re-)Use
The objective of this qualitative study is to create a better understanding of patients' mental model of health data engagement interfaces and tools (such as Dynamic Consent).
- Trial name
- ENGAGE (NCT05229978)
- Testing
- Showing an existing Dynamic Consent (computer interface) as prompt
- Where
- Belgium
- Volunteers
- 23 people, healthy volunteers welcome
- Sponsor
- Universitair Ziekenhuis Brussel
Consent Forms, Anesthesia
Effectiveness of Large Language Model for Anaesthesia and Procedural Consent
Patient understanding of anaesthesia risks remains inconsistent due to time constraints, language barriers, and variable clinician communication styles.
- Conditions
- Consent Forms, Anesthesia, Artificial Intelligence (AI)
- Trial name
- PEAR (NCT06949462)
- Testing
- PEAR
- Where
- 2 sites in Singapore
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Singapore General Hospital
Healthy
Modified Consent Form Utility
Subjects enrolling into a nutrition study of the effects of tea on fat absorption will be randomized to receive either a standard informed consent document or a modified document that is shorter and more easily understood than…
- Trial name
- NCT00715923
- Testing
- Modified consent form, Standard consent form
- Where
- United States
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- University of California, Davis
Consent Form
Strengthening Informed Consent for Authentic Participation in Perinatal HIV Research
This study evaluates a visual Informed Consent Form (ICF) compared to a standard, text-only ICF as an approach to achieving meaningful consent into a clinical trial.
- Trial name
- NCT07122960
- Testing
- Visual ICF, Text-only ICF
- Where
- South Africa
- Volunteers
- 58 people, healthy volunteers welcome
- Sponsor
- Columbia University
Consent Forms
Clinical Informed Consent Format Evaluation
This study evaluates the effectiveness of a patient-centered short written informed consent form and a patient-centered short video informed consent in a randomized controlled trial (control = traditional informed consent ).
- Trial name
- NCT02489682
- Testing
- Long-form written Informed consent information, Short-form written Informed consent information, Video Informed consent information
- Volunteers
- 76 people, healthy volunteers welcome
- Sponsor
- Carnegie Mellon University