Clinical trials: Consent
HIV, PrEP
Self-Consent for PrEP Perspectives
This study involves a one-time, web-based quantitative structured self-complete ("web-based") survey for all subjects and a qualitative semi-structured ("qualitative") interview for a selected sub-sample of subjects to evaluate…
- Trial name
- NCT02801760
- Where
- 11 sites in United States
- Volunteers
- 58 people, healthy volunteers welcome
- Sponsor
- University of North Carolina, Chapel Hill
Informed Consent
Informed Consent and Clinical Trials
To understand the patients' meaning of the informed consent process in clinical trials. Objective of the study is: to assess, in a cohort of subjects included in clinical trials, whether the information and the informed Consent…
- Trial name
- NCT01635842
- Where
- Italy
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- Azienda Usl di Bologna
Healthy
EQUIC-CC: Enhancing Quality of Informed Consent - Customized Consent
Patients in 'parent' cooperative study projects are interviewed about their experiences in the informed consent process.
- Trial name
- NCT00032539
- Where
- 4 sites in United States
- Volunteers
- 240 people, healthy volunteers welcome
- Sponsor
- US Department of Veterans Affairs
Sexual Assault, Alcohol Misuse
Evaluating Cross-Cutting Prevention at the U.S. Air Force Academy
Sexual assault and alcohol misuse are interrelated, persist at high rates in military populations, and carry negative consequences for military units and personnel.
- Trial name
- NCT06875284
- Testing
- Sexual Communication and Consent (SCC), Alcohol eCHECKUP TO GO (eCHECKUP TO GO), Training as usual (TAU)
- Where
- United States
- Volunteers
- 2,041 people
- Sponsor
- RTI International
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
Lymphoma, Hodgkin Disease
Consent for Obtaining Additional Tissue at the Time of a Diagnostic Biopsy
This study is designed to collect tissue samples that may aid in the treatment and learning about various oncology diagnosis.
- Trial name
- NCT01078350
- Testing
- tumor tissue aspiration, phlebotomy
- Where
- United States
- Volunteers
- 93 people
- Sponsor
- Stanford University
Information Disclosure
Paper Versus Cartoon Video-based Administration of Study Information Notice for Participant Consent
This study is a randomized trial in which participants are assigned to one of 2 strategies of information notice administration which include the standard approach versus a video-based cartoon approach.
- Trial name
- CONSENT (NCT05341791)
- Testing
- Cartoon video describing study information notice
- Where
- Cameroon
- Volunteers
- 350 people, healthy volunteers welcome
- Sponsor
- Elizabeth Glaser Pediatric AIDS Foundation
Scoliosis Neuromuscular, Scoliosis Idiopathic
Post-market Clinical Follow-up Study of NEMOST V2
The NEMOST spinal implant is a growth domino intended for the surgical treatment of progressive scoliosis in children. As part of post-market surveillance, EUROS is conducting a retrospective and prospective study to collect…
- Conditions
- Scoliosis Neuromuscular, Scoliosis Idiopathic, Consent Forms
- Trial name
- NEMOST V2 (NCT07403084)
- Testing
- NEMOST V2 growing domino
- Where
- 5 sites in France
- Volunteers
- 140 people
- Sponsor
- EUROS
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
Prostate Biopsy
Impact of Procedure Materials on Patient Anxiety, Depression, and Pain in Prostate Biopsy Consent
The gold standard for diagnosing prostate cancer is an ultrasound-guided prostate biopsy. Despite its low complication rates, the procedure can cause significant stress, discomfort and anxiety in patients.
- Trial name
- NCT06802783
- Testing
- Photo consent
- Where
- Turkey (Türkiye)
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- Marmara University
Respiratory Infections, Diarrhea
High/Low Dose Vit A in Diarrhea/ALRI in Severe PEM
Vitamin A deficiency is an important health problem globally including Bangladesh. The problem is greater among under-five children, particularly in malnourished.
- Conditions
- Respiratory Infections, Diarrhea, Malnutrition
- Trial name
- NCT00388921
- Testing
- Vitamin A
- Where
- Bangladesh
- Volunteers
- 260 people
- Sponsor
- International Centre for Diarrhoeal Disease Research, Bangladesh
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
Staphylococcus Aureus Bacteremia
Evaluating Simplified Layered Consent for Clinical Trials
The goal of this clinical trial (the SIMPLY-SNAP trial) is to compare a simplified layered consent form to a full-length consent form for use during the informed consent process for a larger clinical trial of treatment of…
- Trial name
- SIMPLY-SNAP (NCT06168474)
- Testing
- Simplified layered consent form, Full-length consent form
- Where
- 6 sites in Canada
- Volunteers
- 347 people
- Sponsor
- Sunnybrook Health Sciences Centre
Consent
App-based Consent for Pediatric Clinical Research
This study aims to understand how well app-based consent performs compared to paper-based consent when recruiting families for a clinical research project.
- Trial name
- ConsentApp (NCT05880147)
- Testing
- Consent App, Traditional paper-based consent
- Where
- Canada
- Volunteers
- 120 people
- Sponsor
- University of British Columbia
Normal and Abnormal Tissue
Louisville Cooperative Tissue Biorepository
To provide appropriate collection, storage, and distribution of specimens and medical data to local investigators who have approved IRB protocols for their specific research purposes.
- Trial name
- LCTB (NCT02021916)
- Where
- United States
- Volunteers
- 17,499 people
- Sponsor
- University of Louisville
Anesthesia, Surgery
Pediatric Anesthesia Consent - Visual Aids
Informed consent in pediatric anesthesia is obtained from the caregiver by the anesthesiologist prior to surgery. Studies demonstrate that caregivers often do not fully understand or recall the information (risks and benefits)…
- Trial name
- NCT05774743
- Testing
- Consent with Visual Aid
- Where
- Canada
- Volunteers
- 140 people
- Sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Cleft Palate, Jaw Abnormalities
Improving Informed Consent for Cleft Palate Repair
To determine if providing a written document in addition to the standard oral discussion of surgical risks improves risk recall for the parents/guardians of a child seen in consultation for cleft palate surgery, and if this has…
- Conditions
- Cleft Palate, Jaw Abnormalities, Maxillofacial Abnormalities, Mouth Abnormalities
- Trial name
- NCT02595307
- Testing
- Pamphlet
- Where
- Canada
- Volunteers
- 40 people
- Sponsor
- IWK Health Centre
Surgery, Consent
Determining Parental Attitudes Toward Day of Surgery Consent for Research
There are no studies examining parents' attitudes towards day of surgery consent for research. The purpose of the study is to determine the attitudes parents of potential research participants have toward being approached for day…
- Trial name
- NCT04613505
- Testing
- Semi-structured interview, Same day consent questionnaire
- Where
- Canada
- Volunteers
- 214 people, healthy volunteers welcome
- Sponsor
- The Hospital for Sick Children
Lumbar Puncture, Pediatrics
Video-Assisted Informed Consent for Neonatal Lumbar Puncture
The purpose of this study is to explore the effectiveness of video-assisted neonatal lumbar puncture consent processes against a conventional consent discussion to inform parents about pediatric lumbar puncture in the pediatric…
- Conditions
- Lumbar Puncture, Pediatrics, Emergency Department Patient, Informed Consent
- Trial name
- NCT07074925
- Testing
- Video assisted informed consent, Standard consent
- Where
- United States
- Volunteers
- 100 people
- Sponsor
- University of Texas at Austin
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)