Clinical trials: Research Participation
Atopic Dermatitis
Investigating Participation Patterns of Patients in Atopic Dermatitis Clinical Trials
Clinical trials, specifically focused on atopic dermatitis, are crucial in assessing the safety and efficacy of new treatments. These trials serve as fundamental instruments in determining whether emerging medications outperform…
- Trial name
- NCT06174493
- Where
- United States
- Volunteers
- 500 people
- Sponsor
- Power Life Sciences Inc.
Experience, Life, Dialysis
What Does the Patient Experience Represent for Patients and Caregivers in Dialysis?
The primary objective of this work is to describe the vision, representations, and beliefs of professionals and patients regarding the role and place of the user during their care journey at the Calydial renal health facility.
- Conditions
- Experience, Life, Dialysis, Patient Engagement, Patient Participation
- Trial name
- EnquêteXP (NCT06529887)
- Where
- 4 sites in France
- Volunteers
- 160 people, healthy volunteers welcome
- Sponsor
- Calydial
Pediatric Cancer
Multisite Implementation of COMPRENDO
COMPRENDO (ChildhOod Malignancy Peer Research NavigatiOn) is a multi-site randomized clinical trial (RCT) that uses a Hybrid Type 1 design, to test the effects of a clinical intervention on patient-level outcomes, while exploring…
- Trial name
- COMPRENDO (NCT06055296)
- Testing
- COMPRENDO Peer Navigation Intervention
- Where
- 4 sites in United States
- Volunteers
- 450 people, healthy volunteers welcome
- Sponsor
- University of California, San Diego
Oncology [See Also, Affected System]
Awareness and Attitude of Cancer Patients About Participation in Clinical Research (CR) in Saudi Arabia
Enrollment of patients in CR may be impacted by their levels of awareness and attitude toward participation. Our study aims at assessing the awareness and willingness to participate in CR and identifying the barriers and…
- Trial name
- NCT02042469
- Where
- Saudi Arabia
- Volunteers
- 300 people
- Sponsor
- National Guard Health Affairs
Patient Participation
Electronic Health Record Strategies to Promote Diverse Participation in Research
The purpose of this study is to determine the effectiveness of enhanced features in an online patient portal including banners, a chatbot, and direct to patient message and traditional mailed letters on increasing interest in…
- Trial name
- NCT05348603
- Testing
- Traditional Letter, Direct to Patient Message, Chatbot
- Where
- United States
- Volunteers
- 726,199 people, healthy volunteers welcome
- Sponsor
- Yale University
Rheumatoid Arthritis
Medical Trial: Appraising Medical Trial Experiences of Rheumatoid Arthritis Patients
Historically, participation in clinical trials has been highly skewed towards specific demographic groups. However, research identifying which trial attributes impact participation, in either positive or negative ways, is…
- Trial name
- NCT05398471
- Where
- United States
- Volunteers
- 500 people
- Sponsor
- Power Life Sciences Inc.
Behavior Changes
CONDOR Impact of Dental Practice-Based Research Network
The purpose of this study was to study the use of a Core Questionnaire that included several questions from each PBRN (DPBRN, PEARL, PRECEDENT - collectively know as CONDOR) that had been extracted from questionnaires previously…
- Trial name
- CONDOR PIRG (NCT01201473)
- Where
- 7 sites in United States, Denmark
- Volunteers
- 687 people, healthy volunteers welcome
- Sponsor
- Dental Practice-Based Research Network
D010051, Ovarian Cancer
Validation of ESGO Quality Indicators in Advanced Ovarian Cancer Surgery
This study, organized by the European Society of Gynaecological Oncology (ESGO), evaluates the clinical impact of adherence to ten ESGO-established quality indicators (QIs) in advanced ovarian cancer surgery.
- Conditions
- D010051, Ovarian Cancer, Advanced-stage Ovarian Cancer, FIGO Stages III and IV
- Trial name
- retroESGO ov1 (NCT07567573)
- Testing
- Preoperative Evaluations, Cytoreductive Surgery, Perioperative Management
- Where
- Belgium
- Volunteers
- 11,383 people
- Sponsor
- European Society of Gynaecological Oncology
Post-Traumatic Stress Disorder, Brain Injuries, Traumatic
Patient Participation Beliefs and Post-Traumatic Stress Disorder (PTSD)
This is an exploratory qualitative interview study being conducted with a primary objective of examining perceptions held by active military and veterans regarding help-seeking attitudes and mental health beliefs which influence…
- Trial name
- NCT01419223
- Where
- United States
- Volunteers
- 30 people
- Sponsor
- INTRuST, Post-Traumatic Stress Disorder - Traumatic Brain Injury Clinical Consortium
Anxiety, Depression
Nursing Intervention in the Patient Being Discharged From the Intensive Care Unit
Background: Psychiatric disorders, such as anxiety, depression or post-traumatic stress disorder (PTSD), are common among critical disease survivors.
- Trial name
- NCT04527627
- Testing
- Nursing Empowerment Intervention
- Where
- 3 sites in Spain
- Volunteers
- 178 people
- Sponsor
- Hospital Clinic of Barcelona
Pulmonary Disease
Evaluation and Treatment of Patients With Lung Disease Not Participating in Research
This study was developed in order for the professional-staff at the Pulmonary-Critical Care Medical Branch (PCCMB) of the National Heart, Lung, and Blood Institute to maintain their skills and increase their understanding of lung…
- Trial name
- NCT00001621
- Where
- United States
- Volunteers
- 280 people
- Sponsor
- National Heart, Lung, and Blood Institute (NHLBI)
Parkinson's Disease
Parkinson's Disease in Asian Americans
The ultimate goal of this project is to use the findings to develop culturally appropriate programs and resources that can be disseminated to key stakeholders to improve access to PD care and increase inclusivity in PD research…
- Trial name
- NCT05532982
- Testing
- Interviews and Surveys
- Where
- United States
- Volunteers
- 430 people, healthy volunteers welcome
- Sponsor
- Tufts University
Preterm Infant
Development, ADL, Participation, and Quality of Life in Preterm Infants: Longitudinal Research
The three fundamental goals of early rehabilitation for preterm infant after leaving NICU are: optimizing function within each child's prognostic potential, preventing the development of secondary conditions that impact life-long…
- Trial name
- NCT06532695
- Testing
- No intervention will be provided.
- Where
- Taiwan
- Volunteers
- 210 people, healthy volunteers welcome
- Sponsor
- Chang Gung Memorial Hospital
Sleep
Addressing Health Disparities in African Americans - Exploring Sleep and Developing Interventions
The purpose of the HD-SLEEP1 study is to help researchers understand what African Americans know and think about sleep. The investigators also want to know how to encourage people to participate in research studies designed to…
- Trial name
- HD-SLEEP1 (NCT05102175)
- Testing
- Focus Group
- Where
- United States
- Volunteers
- 36 people, healthy volunteers welcome
- Sponsor
- Pennington Biomedical Research Center
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
Musculoskeletal Diseases, Osteoarthritis, Knee
Effect of Research Participation Versus Usual Clinical Treatment on Pain in Patients With Musculoskeletal Disorders
This study explores the effects on pain, function and illness perceptions, of participating in clinical research versus being treated with standard care in patients with musculoskeletal disorders.
- Conditions
- Musculoskeletal Diseases, Osteoarthritis, Knee, Illness Perceptions
- Trial name
- NCT03785561
- Testing
- participation in a health research study
- Where
- Denmark
- Volunteers
- 1,850 people
- Sponsor
- Frederiksberg University Hospital
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
Alzheimer Disease
Alzheimer's Disease and Precision Medicine Research Among Native People
This project intends to address the gaps in Alzheimer's disease (AD) and precision medicine (PM) research in American Indian and Alaska Native (AI/AN) populations by comparing written and video-based materials for recruitment…
- Trial name
- NCT03448601
- Testing
- Culturally tailored brochure intervention group, Culturally tailored video intervention group
- Where
- United States
- Volunteers
- 523 people, healthy volunteers welcome
- Sponsor
- University of Colorado, Denver
Unilateral Cerebral Palsy
Wereables for Upper Limb Functionality in Hemiparesis
The project is configured as a national interventional study that aims to determine the effectiveness of an intervention strategy using wearable technology, tailored to improve function (WeFun-wearable), on the spontaneous use of…
- Trial name
- WeFun (NCT06872736)
- Testing
- WeFun-wearable activated, WeFun-wearable desactivated
- Where
- Spain
- Volunteers
- 40 people
- Sponsor
- Universidade da Coruña
Craniocerebral Trauma
Intensive Rehabilitation of Patients With Severe Traumatic Brain Injury - Development of a Didactic Model
The aim of the study is to develop a research-based pedagogic model to improve the interaction between the patient's motivation, influence and learning.The hypothesis is: A neuro-rehabilitation effort in patients with severe…
- Trial name
- NCT00419939
- Where
- Denmark
- Volunteers
- 11 people
- Sponsor
- University of Aarhus