Clinical trials: Consent of Patients
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
Pregnancy, Informed Consent
Optimizing Timing of Cesarean Delivery Consent on Labor and Delivery
Nationally, 32.1% of pregnant patients deliver via cesarean delivery, including both patients who undergo a planned cesarean delivery and patients who intend to undergo vaginal delivery and are recommended to deliver via cesarean…
- Trial name
- NCT07117708
- Testing
- Early Surgical Consent, Surgical Consent if Clinically Indicated
- Where
- United States
- Volunteers
- 200 people
- Sponsor
- Duke University
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
Consent of Patients, Coercion to Participate in Research
Coercion in Same-Day Research Consent
As a result of their unique practice patterns, many specialist physicians typically only meet patients on the date of an intervention such as surgery.
- Trial name
- NCT07380035
- Testing
- Invitation to Consent to Trial Participation
- Where
- Canada
- Volunteers
- 114 people
- Sponsor
- University of Toronto
Consent Process
Examining the Efficacy of a Digital Media Intervention to Increase Recruitment Rates
WHEAT-Boost is a Study Within A Trial (SWAT) that aims to improve how families are recruited into neonatal research studies by testing a new way of sharing information.
- Trial name
- WHEAT-Boost (NCT07284329)
- Testing
- Intervention (Video) Arm
- Where
- 15 sites in Canada
- Volunteers
- 787 people
- Sponsor
- IWK Health Centre
Informed Consent, HIV Infections
Community Solutions to Adolescent Research Consent - Minor Consent for Biomedical HIV Research
Public deliberation is a novel method for engaging the public in collective decision-making. Its goal is to facilitate debate and discussion that: 1) fosters the formation of reasonable and informed opinions, 2) permits…
- Trial name
- C-START (NCT05371327)
- Testing
- Public deliberation
- Where
- United States
- Volunteers
- 128 people
- Sponsor
- Indiana University
Aneuploidy, Genetic Counseling
GEM: Impact of a Video Education Tool on Decisional Conflict Among Prenatal Patients
The goal of this randomized clinical trial is to assess the impact of a video educational tool on patient decisional conflict at the time when making a decision about prenatal genetic testing.
- Conditions
- Aneuploidy, Genetic Counseling, Informed Consent, Decisional Conflict
- Trial name
- GEM (NCT06771453)
- Testing
- Video Educational Tool Regarding Prenatal Genetics
- Where
- United States
- Volunteers
- 140 people, healthy volunteers welcome
- Sponsor
- Women and Infants Hospital of Rhode Island
Informed Consent, Preference, Patient
Patient Preferences on Same-day Bilateral Intravitreal Dexamethasone Injections
Intravitreal injections with dexamethasone implant (Ozurdex®) provide a reasonable and long-lasting treatment option in the cases of diabetic macular edema, as well as macular edema resulting from retinal vein occlusion and…
- Trial name
- NCT06894017
- Testing
- Ozurdex (dexamethasone)
- Where
- Denmark
- Volunteers
- 200 people
- Sponsor
- Copenhagen University Hospital, Rigshospitalet
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
Informed Consent Process
Comparing AI Role-Play and Peer Role-Play for Informed Consent Training in Endoscopy: A Randomized Control Trial
The goal of this randomized controlled trial is to find out whether AI-based role play is effective in teaching healthcare trainees how to obtain informed consent from patients for endoscopic procedures.
- Trial name
- NCT07069504
- Testing
- AI-based role play, Peer role play
- Where
- Canada
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- The Hospital for Sick Children
Informed Consent in Neurosurgery
Educational Informed Consent Video in Neurosurgery
This single-center randomized controlled trial addresses a critical gap in neurosurgical practice by evaluating the effectiveness of video-assisted informed consent compared to standard consent procedures.
- Trial name
- NCT07064252
- Testing
- Educational Informed Consent Video, Standard informed consent
- Where
- Switzerland
- Volunteers
- 171 people
- Sponsor
- Felix C. Stengel, MD
Understanding of Consent in Clinical Research, Implementation of Video-Consent in Clinical Research
Impact of Video-Enhanced Consent on Informed Decision-Making for Parents of Extremely Preterm Infants Eligible for the ViDES Study
This pilot randomized controlled trial evaluates the impact of video-enhanced consent compared to the usual approach. The investigators aim to assess if video-enhanced consent empowers decision-making and improves understanding…
- Trial name
- NCT06446492
- Testing
- ViDEO explaining study, Usual Care
- Where
- United States
- Volunteers
- 83 people, healthy volunteers welcome
- Sponsor
- The University of Texas Health Science Center, Houston
Violence Against Children, Sexual Violence
How do Adults Sexual Offender Against Pre-pubescent Minors Perceive the Notion of Consent Based on the Account of Their Lived Experience ? (SOconsent)
In 2024, the police and gendarmerie recorded 12,260 victims of sexual violence, an increase of 7% compared with 2023. In 2019, 36,000 cases of sexual violence (rape or sexual assault) were handled by the public prosecutor's…
- Conditions
- Violence Against Children, Sexual Violence, Consent
- Trial name
- SOconsent (NCT07035717)
- Testing
- Patient interview
- Where
- France
- Volunteers
- 20 people
- Sponsor
- University Hospital, Montpellier
Malocclusion, Dentofacial Deformities
Augmented Reality for Orthognatic Surgery Patient Education
To evaluate whether the use of augmented reality (AR) for visualizing 3D models can be a valuable addition to patient education regarding orthognathic procedures compared to using only 2D visualization (on a computer screen).
- Conditions
- Malocclusion, Dentofacial Deformities, Patient Satisfaction, Informed Consent
- Trial name
- NARRATE (NCT06140043)
- Testing
- Patient consultation
- Where
- 3 sites in Germany, Netherlands
- Volunteers
- 60 people
- Sponsor
- University Medical Center Groningen
Informed Consent
Effectiveness of Immersive Virtual Reality in Nursing Students' Learning
Teaching using VR for basic cardiopulmonary resuscitation and patient examination (experimental group) will not result in differences in knowledge and skill acquisition compared to traditional classroom-based simulation teaching…
- Trial name
- UBUJIRV25 (NCT06839573)
- Testing
- Experience with virtual reality glasses
- Volunteers
- 140 people, healthy volunteers welcome
- Sponsor
- Universitat Jaume I
Pathologically Confirmed Differentiated Thyroid Carcinoma, All Patients Are in the Initial Treatment Phase
The Effect of a Psychosomatic Symptom Intervention Program on the Primary Treatment of Differentiated Thyroid Cancer
The psychosomatic symptoms of patients with differentiated thyroid cancer (DTC) during the initial treatment phase need to be improved.
- Conditions
- Pathologically Confirmed Differentiated Thyroid Carcinoma, All Patients Are in the Initial Treatment Phase, Normal Cognitive and Communicative Abilities, Capable of Reading and Understanding Questionnaires in Chinese, Ability to Use a Smartphone
- Trial name
- NCT06422702
- Testing
- Psychosomatic Symptoms Intervention, Extended supportive care
- Where
- China
- Volunteers
- 84 people
- Sponsor
- Harbin Medical University
Consent Form, Lung Cancer
Education Intervention in Patients with Rash Due to Epidermal Growth Factor Receptor (EGFR) Treatment.
The main adverse reaction of EGFR seen in patients is rash. EGFR treated patients have a 24-95% incidence of rash depending on the type of treatment they receive.
- Conditions
- Consent Form, Lung Cancer, Colon Cancer, Pancreas Cancer
- Trial name
- NCT03992664
- Testing
- Educational training program
- Where
- Cyprus
- Volunteers
- 40 people
- Sponsor
- Cyprus University of Technology
VR-based Informed Consent
Virtual Reality for Patient Informed Consent in Neurosurgery
The goal of this randomized controlled trial is to evaluate benefits of VR (virtual reality)-based patient informed consent in neurosurgery regarding subjective patient comprehension, patient-doctor relationship and anxiety.
- Trial name
- NCT06627426
- Testing
- VR-based patient informed consent
- Where
- Switzerland
- Volunteers
- 34 people
- Sponsor
- University Hospital, Basel, Switzerland
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
Informed Consent, Patient and Caregiver Satisfaction
Evaluating Patient and Caregiver Satisfaction with the Informed Consent Process in Surgery
The goal of this observational study is to evaluate patient and caregiver satisfaction with the informed consent process in surgical practice at a tertiary care center in Nepal.
- Trial name
- NCT06746207
- Testing
- Informed Consent Process Evaluation
- Where
- Nepal
- Volunteers
- 384 people
- Sponsor
- Maharajgunj Medical Campus