Clinical trials: Consent
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
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
Sexual Health, Sexual Consent
Boys Sexual Health
Sexual health among young people is an important issue for healthcare professionals, educators, and society. The purpose of this study was to examine the effects of a mobile application on emerging adult men's sexual knowledge…
- Conditions
- Sexual Health, Sexual Consent, Intervention Effectiveness, Mobile Application
- Trial name
- boys (NCT07915180)
- Testing
- Boy's serious game
- Where
- Taiwan
- Volunteers
- 174 people, healthy volunteers welcome
- Sponsor
- Kaohsiung Medical University Chung-Ho Memorial Hospital
Surveys and Questionnaires, Noncommunicable Diseases
Use of Consent Language and Mode to Improve Interactive Voice Response Survey in Colombia and Uganda
This study evaluates the effect of one new form of introduction language and three new modes of providing consent on interactive voice response (IVR) survey cooperation, response, refusal and contact rates, as compared to control…
- Trial name
- NCT04394520
- Testing
- Modified Introduction, Active Opt-in, Active Opt-out
- Where
- 2 sites in Colombia, Uganda
- Volunteers
- 3,786 people, healthy volunteers welcome
- Sponsor
- Johns Hopkins Bloomberg School of Public Health
Labour Pain
Spoken Animation for Labour Epidural
The purpose of this study is to evaluate a new animated information film as a tool for introducing the concept of epidural as a method of labour pain relief to expectant women.
- Trial name
- SALE (NCT07202221)
- Testing
- Participant views Epidural animation before reading gold standard written information, Participant receives current gold standard written information alone
- Where
- United Kingdom
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Chelsea and Westminster NHS Foundation Trust
Biospecimen Donation
Preferred Consent Models for Secondary Uses of Biospecimens Among Diverse Women
Research with stored biospecimens can provide substantial societal benefits, including greater understanding of cancer etiology and discovery of new cancer therapies, but one critical social and ethical issue is the use of…
- Trial name
- NCT02205749
- Testing
- Study-specific consent model, Broad consent model, Notice consent model
- Where
- United States
- Volunteers
- 302 people, healthy volunteers welcome
- Sponsor
- Washington University School of Medicine
Cultural Competency
Sign Here: How to Conduct Informed Consent With Deaf Individuals
The goal of this research is to create a training film for hearing healthcare providers to teach them how to competently and sensitively interact with Deaf patients.
- Trial name
- NCT05268055
- Testing
- "Sign Here" training intervention, Intervention as usual
- Where
- United States
- Volunteers
- 208 people, healthy volunteers welcome
- Sponsor
- University of Massachusetts, Worcester
Healthy, Informed Consent
EQUIC-SM: Enhancing Quality of Informed Consent
Patients in 'parent' cooperative studies projects are interviewed about their experiences in the informed consent process.
- Trial name
- EQUIC (NCT00032565)
- Where
- 22 sites in United States
- Volunteers
- 836 people, healthy volunteers welcome
- Sponsor
- US Department of Veterans Affairs
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
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
Parturient Who Underwent Epidural Anesthesia During Which an Unintentional Dural Punctur Occurred, Parturient Who Develop a Postdural Puncture Headache
Chronic Headache and Chronic Backache Following Unintentional Dural Puncture at Delivery Room.
he study is a telephone questionnaire. The study will include 400 women, 100 in each group. OBJECTIVE: To investigate the prevalence of chronic and chronic back pain following PDPH accidental dural puncture during epidyral…
- Conditions
- Parturient Who Underwent Epidural Anesthesia During Which an Unintentional Dural Punctur Occurred, Parturient Who Develop a Postdural Puncture Headache, Parturient Who Gave Informed Consent to Participation in the Study
- Trial name
- NCT03908424
- Testing
- Epidural Blood patch.
- Where
- Israel
- Volunteers
- 389 people, healthy volunteers welcome
- Sponsor
- Shaare Zedek Medical Center
Healthy Volunteers, Participant Satisfaction
Evaluating the Quality of Different Methods of Obtaining Informed Consent
This is a sub-study of a drug development study conducted by Pfizer, Inc. It will evaluate how well people who participate in research studies understand from the study consent form what the purpose of the study is, the risks and…
- Trial name
- NCT00794729
- Where
- United States
- Volunteers
- 250 people, healthy volunteers welcome
- Sponsor
- National Institutes of Health Clinical Center (CC)
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
HIV Infections
Computer-Generated Vs. Standard Informed Consent for HIV Research Studies
The purpose of this study is to test an interactive multimedia informed consent (iMIC) computer program to see if the program can generate a consent form that potential participants in an HIV trial can understand.
- Trial name
- NCT00104559
- Testing
- iMIC-generated consent form and tutorial, Standard paper consent form
- Where
- United States
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- National Institute of Allergy and Infectious Diseases (NIAID)
Living Donors, Tissue Donors
RELIVE Informed Consent Study
An organ transplant is frequently the best option and, in some cases, the only option to save the lives of transplant recipients.
- Trial name
- NCT01742234
- Testing
- Organ Donation
- Volunteers
- 624 people, healthy volunteers welcome
- Sponsor
- National Institute of Allergy and Infectious Diseases (NIAID)
Satisfaction, Risk Reduction
Electronic Confirmed Versus Conventional Consenting Process: A Randomized Controlled Trial
· The target population for our study is women who present in their last clinic visit before delivery and are scheduled for an elective cesarean section.
- Trial name
- ECCCO (NCT03510260)
- Testing
- Study Group I, Study Group II, Control Group
- Where
- United States
- Volunteers
- 105 people, healthy volunteers welcome
- Sponsor
- The University of Texas Medical Branch, Galveston
Consent, Laparoscopic
Optimizing the Consent Process for Emergent Laparoscopic Cholecystectomy
The Canadian Medical Protective Association (CMPA) defines informed consent (IC) as a voluntary process where important elements include details of the procedure, complications, and proposed alternatives.
- Conditions
- Consent, Laparoscopic, Cholecystectomy
- Trial name
- NCT04852016
- Testing
- Consent process with the addition of Digital educational platform (DEP), Consent process using the standard verbal consent (SVC)
- Where
- Canada
- Volunteers
- 79 people, healthy volunteers welcome
- Sponsor
- Dr. Boris Zevin
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
Bariatric Surgery Candidate
Video-Assisted Presentation Before Bariatric Surgery Enhanced Understanding of Informed Consent Content
This study evaluates the addition of video presentation on conventional informed consent. Participants divided two randomly, one group read only conventional informed consent, the other video presentation was watched after…
- Trial name
- NCT03653962
- Testing
- video assisted group, non-video group
- Volunteers
- 77 people, healthy volunteers welcome
- Sponsor
- Inonu University