Clinical trials: Feasibility Study
PTSD, Critical Illness
The Experiences of Children and Caregivers Given PICU Storybooks
1. To assess the acceptability and feasibility of a study design aimed at evaluating the efficacy of a newly developed intervention for children and their caregivers following discharge from PICU 2.
- Conditions
- PTSD, Critical Illness, Depression, Anxiety
- Trial name
- NCT04041401
- Testing
- PICU storybook
- Where
- United Kingdom
- Volunteers
- 24 people, healthy volunteers welcome
- Sponsor
- University of Surrey
Automobile Driving
Driving Ability Evaluation System to Improve the Conditional Driving License System: Feasibility Study of High-risk Drivers.
The primary objective of this study is to verify the safety and validity of a VR driving simulator developed for evaluating the driving abilities of elderly drivers.
- Trial name
- NCT06290037
- Testing
- VR Driving Simulator, Computerized Neurocognitive Function Test, Driver Test Station
- Where
- South Korea
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Seoul National University Hospital
Fear of Falling
Feasibility of Aktiv Gegen Sturzangst (AGES) in Assisted Living Facilities
Aktiv Gegen Sturzangst (AGES) is a multicomponent group intervention combining cognitive behavioral therapy and structured exercise to address fear of falling in older adults receiving services from assisted living facilities.
- Trial name
- AGES (NCT07787819)
- Testing
- Multicomponent fear of falling intervention
- Where
- 3 sites in Switzerland
- Volunteers
- 19 people, healthy volunteers welcome
- Sponsor
- Eric Lenouvel
Stress
Nurse Health Pilot: Feasibility and Acceptability of a Virtual ACT-intervention in Nurses During COVID-19
Frontline nurses increasingly face challenges between executing their jobs to the best of their ability and caring for their own physical and mental health.
- Trial name
- NHP (NCT04821037)
- Testing
- ACT
- Where
- Switzerland
- Volunteers
- 10 people, healthy volunteers welcome
- Sponsor
- Prof. Dr. Andrew Gloster
HIV-1-infection
Postpartum Pre-exposure Prophylaxis (PrEP) Study to Evaluate an Adherence Promotion Package for Postpartum Women on PrEP
The postpartum PrEP study (PPS) seeks to evaluate how best to improve adherence to PrEP in postpartum women and to evaluate how acceptable it is to offer HIV self tests for the participant and partner, and provide enhanced…
- Trial name
- PPS (NCT04897737)
- Testing
- HIVST and enhanced adherence biofeedback, Orasure/UrSure test
- Where
- South Africa
- Volunteers
- 106 people, healthy volunteers welcome
- Sponsor
- University of California, Los Angeles
Breast Engorgement, Lactation Disorders
Lymphatic Drainage Versus Ultrasound for Postpartum Breast Engorgement: A Pilot Study
In this article, women were randomly assigned to the manual lymphatic drainage group, therapeutic ultrasound group, and control group, and the breast pain, swelling hardness, and milk excretion before and after each treatment…
- Trial name
- NCT06129344
- Testing
- Manual Lymphatic Drainage Group, Ultrasound therapy group
- Where
- Taiwan
- Volunteers
- 31 people, healthy volunteers welcome
- Sponsor
- National Yang Ming Chiao Tung University
Tattoo, Healthy
Safety and Efficacy Study of a New Device for Tattoo Removal
A new mechanical device is evaluated for tattoo removal, comparing two types of needle washing fluids. 30 healthy subjects with tattoos will be treated.
- Trial name
- NCT00409162
- Testing
- Eraser TM device, with washing fluid
- Where
- Israel
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Assaf-Harofeh Medical Center
HIV/AIDS, Adolescent Behavior
Youth Power Action Feasibility Study of Online Support Group Intervention Among Adolescents Living With HIV in Nigeria
This study will examine the feasibility and acceptability of an intervention designed to improve retention in HIV care services and improve anti-retroviral therapy (ART) adherence among adolescents ages 15-19 years living with…
- Conditions
- HIV/AIDS, Adolescent Behavior, Medication Adherence, Health Behavior
- Trial name
- NCT03076996
- Testing
- Online support group
- Where
- Nigeria
- Volunteers
- 41 people, healthy volunteers welcome
- Sponsor
- FHI 360
Eye Pain
Study of the ETX-4143 2.0 Device in Subjects With Eye Pain
A prospective early-feasibility study to evaluate the safety and effectiveness of the ETX-4143 2.0 device. The device is intended to treat subjects with eye pain
- Trial name
- NCT06479382
- Testing
- ETX-4143 2.0
- Where
- 4 sites in Australia
- Volunteers
- 31 people, healthy volunteers welcome
- Sponsor
- EyeCool Therapeutics, Inc.
Training Effectiveness
Proficiency-Based Progression on Hugo Ras Robot for Learning Nerve-Sparing RARP: Feasibility Study
Feasibility study 1. To evaluate the feasibility of PBP training for nerve-sparing RARP on the Hugo Ras system 2. To assess time to proficiency for participants with varying experience 3.
- Trial name
- NCT07180797
- Where
- Belgium
- Volunteers
- 12 people, healthy volunteers welcome
- Sponsor
- Orsi Academy
Adrenal Insufficiency
Neonatal, Infant and Toddler Salivary Study (NITS Study)
Currently, the only way to analyse glucocorticoids for the screening or diagnosis of AI in young children is via plasma obtained by invasive capillary or venous blood sampling.
- Trial name
- NITS (NCT05350982)
- Testing
- SalivaBio +/- SaliPac
- Where
- United Kingdom
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Sheffield Children's NHS Foundation Trust
Retinal Diseases, Fuchs Endothelial Dystrophy
DISCOVER Study: Microscope-integrated Intraoperative OCT Study
Optical coherence tomography (OCT )provides high resolution information regarding the anatomic structure of the tissues of the eye in a cross-sectional and 3 dimensional view.
- Conditions
- Retinal Diseases, Fuchs Endothelial Dystrophy, Macular Hole, Epiretinal Membrane
- Trial name
- DISCOVER (NCT02423213)
- Where
- United States
- Volunteers
- 2,911 people, healthy volunteers welcome
- Sponsor
- The Cleveland Clinic
History-taking Training, GPT
Simulated Patient and AI-based Roleplay for History-taking
The goal of this clinical trial is to evaluate whether AI-based simulated patient training can improve clinical reasoning and history-taking skills in medical students.
- Conditions
- History-taking Training, GPT, Medical Education
- Trial name
- SPAR-H (NCT06766383)
- Testing
- GPT-simulated patients, traditional role-playing
- Where
- China
- Volunteers
- 56 people, healthy volunteers welcome
- Sponsor
- zhen wang
Gait, Unsteady
Home-based Motor Imagery for Gait Stability in Older Adults. A Cross-over Feasibility Study. (MIGS-F)
Gait stability is reduced as early as from age 40 to 50. Gait stability can be improved in patients with neurological diseases or in healthy elderly persons with exercises.
- Trial name
- MIGS-F (NCT02693756)
- Testing
- Motor imagery
- Where
- Switzerland
- Volunteers
- 32 people, healthy volunteers welcome
- Sponsor
- University of Applied Sciences of Western Switzerland
Spinal Cord Injuries
Patient Self-managed BCI-FES
This study aims to assess the feasibility of therapist-caregiver-patient training to use BCI and FES technology with a view to the inexpensive equipment eventually being used for home use by tetraplegic patients as a continuing…
- Trial name
- NCT03257982
- Testing
- BCI-FES hand therapy
- Where
- United Kingdom
- Volunteers
- 22 people, healthy volunteers welcome
- Sponsor
- NHS Greater Glasgow and Clyde
Breast Cancer, Bowel Cancer
EQUITA - A Feasibility Trial of a Faith-placed Intervention to Increase Screening Uptake in Black Adults
The goal of this randomised feasibility trial is to examine feasibility and acceptability of a co-produced and faith-placed intervention to increase uptake of breast, cervical, bowel, and abdominal aortic aneurysm (AAA) screening…
- Conditions
- Breast Cancer, Bowel Cancer, Cervical Cancer, Abdominal Aortic Aneurysm
- Trial name
- EQUITA (NCT06981182)
- Testing
- Faith-placed intervention to promote breast, cervical, bowel, and AAA screening uptake in Black communities.
- Where
- 3 sites in United Kingdom
- Volunteers
- 300 people, healthy volunteers welcome
- Sponsor
- University of Sunderland
Induction of Labor Affected Fetus / Newborn
Dilapan-S® for Induction of Labor The Feasibility Study
This is a prospective feasibility study to investigate Dilapan-S® as an outpatient method of cervical ripening in low risk pregnancies >=39 weeks.
- Trial name
- DILATE (NCT04521062)
- Testing
- Dilapan S
- Where
- United States
- Volunteers
- 22 people, healthy volunteers welcome
- Sponsor
- Albany Medical College
Eating Disorders in Children
Feasibility and Acceptability of the BE REAL Let's Eat Curriculum in Middle Schoolers
The purpose of this study is to evaluate the feasibility and acceptability of 'Let's Eat' and its capacity to change eating behavior and body appearance/functionality considerations in adolescents aged 11-14 years.
- Trial name
- NCT07615088
- Testing
- Let's Eat Nutrition Curriculum
- Where
- 2 sites in United States
- Volunteers
- 138 people, healthy volunteers welcome
- Sponsor
- University of North Carolina, Charlotte
Domestic Violence, Child Maltreatment
RISE With Residents
Prevention of child maltreatment (CM) remains a public health priority in Canada; approximately one-third of Canadians report exposure to at least one form of CM.
- Conditions
- Domestic Violence, Child Maltreatment, Pediatric ALL, Psychiatry
- Trial name
- RISE Residents (NCT05490121)
- Testing
- Violence, Evidence, Guidance, Action Project (VEGA) Education Intervention
- Where
- Canada
- Volunteers
- 84 people, healthy volunteers welcome
- Sponsor
- McMaster University
Vaginal Atrophy
Clinical Performance and Safety of the VITA AV Clinical System
The primary objective of this clinical investigation is to demonstrate that treatment with the VITA AV clinical system is feasible and to evaluate clinical performance and safety when used to improve the symptoms and signs of…
- Trial name
- NCT06207227
- Testing
- VITA AV Clinical System
- Where
- Georgia
- Volunteers
- 12 people, healthy volunteers welcome
- Sponsor
- AVeta Medical
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