Clinical trials: Recruitment of Participants
Survey
Using Survey to Explore Perceptions of Adults With Low Socioeconomic Status Regarding the NutriQuébec Study
Populations with low socioeconomic status (SES) are more likely to develop diseases across lifespan and are frequently underrepresented in large cohort studies.
- Trial name
- NCT03847584
- Testing
- Survey
- Where
- Canada
- Volunteers
- 418 people, healthy volunteers welcome
- Sponsor
- Laval University
BLS, Recruitment
Socio-demographic Characteristics of Basic Life Support Course Participants
Aim The aim of the study is to characterize the typical basic life support (BLS) course participant. The characterization include age, sex, education, ethnicity, income, health care data and cohabitation.
- Trial name
- NCT04251325
- Testing
- Basic Life Support Courses
- Where
- Denmark
- Volunteers
- 900,000 people
- Sponsor
- Emergency Medical Services, Capital Region, Denmark
Cardiovascular Diseases
Does Paying Subjects to Participate in Research Improve Recruitment
Patient recruitment into clinical trials is a major challenge and the elderly, socially deprived and those with multiple co-morbidities are often under-represented.
- Trial name
- NCT03881969
- Testing
- Financial Payment of £100
- Volunteers
- 1,015 people
- Sponsor
- University of Dundee
Focus Groups
Using Focus Groups to Explore Perceptions of Adults With Low Socioeconomic Status Regarding the NutriQuébec Study
NutriQuébec is a web-based prospective cohort study aiming to monitor and analyse the evolution of Québec population eating habits through annual questionnaires.
- Trial name
- NCT03849846
- Testing
- Focus groups
- Where
- Canada
- Volunteers
- 28 people, healthy volunteers welcome
- Sponsor
- Laval University
Parkinson Disease
University of Delaware Parkinson's Disease Registry
The purpose of this Parkinson's Disease Registry is to assist with recruitment of willing participants into future Parkinson's disease research studies at the University of Delaware.
- Trial name
- NCT04496973
- Where
- United States
- Volunteers
- 1,000 people
- Sponsor
- University of Delaware
Family Members, Recruitment
Clinical Trial Recruitment and Retention Strategies for Family Members in the ICU
There is a need to identify strategies that improve the conduct of clinical trials involving family members of intensive care unit (ICU) patients.
- Conditions
- Family Members, Recruitment, Clinical Study, Retention
- Trial name
- SWAT (NCT06588101)
- Testing
- Written informed consent with infographic, Compensation
- Where
- Canada
- Volunteers
- 160 people
- Sponsor
- Lady Davis Institute
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
Caregiver Stress, Caregiver Health Related QOL
Applying CSNAT in HBPC as an Approach to Elder Mistreatment Risk Reduction
This study will evaluate the feasibility, acceptability, and preliminary effects of the Carer Support Needs Assessment Tool (CSNAT) intervention for family caregivers of older adults receiving home-based primary care.
- Conditions
- Caregiver Stress, Caregiver Health Related QOL, Caregiver Mental Health, Caregiver Health Status
- Trial name
- NCT07749482
- Testing
- CSNAT-I
- Where
- United States
- Volunteers
- 80 people, healthy volunteers welcome
- Sponsor
- The University of Texas Medical Branch, Galveston
Recruitment of Participants
The Influence of Different Preoperative Decision Schemes on the Visual Quality After Toric Intraocular Lens Implantation
To study the Influence of Different Preoperative Decision Schemes on the Visual Quality After Toric Intraocular Lens Implantation
- Trial name
- NCT04006912
- Testing
- phacoemulsification and Toric intraocular lens implantation
- Where
- China
- Volunteers
- 60 people
- Sponsor
- Second Affiliated Hospital, Zhejiang University, School of Medicine
Glaucoma
Interactive Study to Increase Glaucoma Adherence to Treatment
Study participants who receive the I-SIGHT intervention will have higher rates of glaucoma treatment compliance (e.g., medication-taking and refill compliance, return for clinical follow-up) and more positive eye health outcomes…
- Trial name
- I-SIGHT (NCT00794170)
- Testing
- Telephone and Print based intervention
- Where
- 2 sites in United States
- Volunteers
- 312 people, healthy volunteers welcome
- Sponsor
- Emory University
Any Disease or Condition, Healthy
UCSF Research Participant Registry
The UCSF Clinical and Translational Science Institute (CTSI) Consultation Service provides recruitment services and facilitates the enrollment of research participants into UCSF clinical studies.
- Trial name
- NCT01717378
- Where
- United States
- Volunteers
- 1,541 people, healthy volunteers welcome
- Sponsor
- University of California, San Francisco
Mentalization, Recruitment of Participants
ATTACH in Denmark: A Feasibility Randomized Controlled Trial
The goal of this feasibility randomized controlled pilot trial is to learn whether the trial can be done as planned, and to investigate if the 10-session parenting program "ATTACH(TM) increases mentalizing skills (the ability to…
- Conditions
- Mentalization, Recruitment of Participants, Adherence, Treatment, Drop Out
- Trial name
- AiD (NCT07162493)
- Testing
- ATTACH, Treatment as Usual (TAU)
- Where
- 3 sites in Denmark
- Volunteers
- 52 people
- Sponsor
- Johanne Smith-Nielsen
Recruitment of Participants
Study of the Correlation Between Preoperative Precise Biometrics, Spatial Assessment and Postoperative Visual Quality in Cataract Patients
This study summarizes the experience of precision treatment and postoperative management of various types of cataract, and intend to further improve the quality of Clinical Cataract diagnosis and treatment.
- Trial name
- NCT04833491
- Where
- China
- Volunteers
- 1,000 people, healthy volunteers welcome
- Sponsor
- Second Affiliated Hospital, Zhejiang University, School of Medicine
Demographic Data, History of Medical and Mental Health
VISN 19 MIRECC Research Database
The VISN 19 MIRECC is involved in research concerned with suicide prevention in high risk populations (e.g., history of traumatic brain injury, post-traumatic stress disorder); Recruitment for future studies will continue with a…
- Conditions
- Demographic Data, History of Medical and Mental Health, History of Combat Experience, History of Suicide
- Trial name
- Repository (NCT01334476)
- Where
- 2 sites in United States
- Volunteers
- 5,000 people
- Sponsor
- VA Eastern Colorado Health Care System
Substance Abuse, Disorders
Screening Protocol for the Evaluation of Research Participants
Background: The National Institute on Drug Abuse (NIDA) uses a standardized set of procedures to develop a pool of potential participants for research studies.
- Trial name
- NCT01036217
- Where
- United States
- Volunteers
- 55,000 people, healthy volunteers welcome
- Sponsor
- National Institute on Drug Abuse (NIDA)