Clinical trials: Waitlist
Latent Tuberculosis Infection, Infection in Solid Organ Transplant Recipients
"Efficacy and Safety of Levofloxacin vs Isoniazid in Latent Tuberculosis Infection in Liver Transplant Patients".
A multicenter, prospective, non-inferiority, randomized and open clinical trial comparing levofloxacin with isoniazid in the treatment of latent tuberculosis infection in patients eligible for liver transplantation.
- Trial name
- FLISH-ILT (NCT01761201)
- Testing
- Levofloxacin, Isoniazid
- Where
- 18 sites in Spain
- Volunteers
- 68 people
- Sponsor
- Fundación Pública Andaluza para la gestión de la Investigación en Sevilla
Subjective Cognitive Complaints, Cancer
Emotional Freedom Techniques to Reduce Patient Reported Cognitive Complaints in Cancer Survivors
The aim of this study is to further validate the CDT as a screening tool for identifying elderly cancer patients in need of a more in-depth cognitive evaluation within comprehensive geriatric assessment (CGA) and to validate the…
- Trial name
- EMOTICON (NCT02771028)
- Testing
- Emotional Freedom Techniques
- Where
- 3 sites in Belgium
- Volunteers
- 121 people
- Sponsor
- General Hospital Groeninge
Mobility Limitation
TIME™ at Home Randomized Controlled Trial
The goal of this randomized controlled trial is to compare the short-term effects of a virtual, community-based, task-oriented group exercise program (TIME™ at Home) with a waitlist control in community-dwelling adults with…
- Trial name
- NCT06245135
- Testing
- TIME at Home
- Where
- 4 sites in Canada
- Volunteers
- 200 people
- Sponsor
- University of Toronto
Health Behavior
The Effects of a Personalized Sleep Improvement App From SleepScore Labs
The study is a single-blinded randomized waitlist controlled trial that aims to assess changes in objective and self-report sleep improvement through use of a dynamic and personalized sleep improvement smartphone app and advice…
- Trial name
- NCT05195359
- Testing
- Dein Schlaf. Dein Tag. sleep improvement application powered by SleepScore
- Where
- Germany
- Volunteers
- 637 people, healthy volunteers welcome
- Sponsor
- ResMed
Primary Prevention, Stress
Efficacy of Taiji Training as a Program for Stress Prevention
Background: Excessive exposure to psychosocial stress can be a potent trigger for somatic diseases and psychological disorders, a cause for missing work, and eventually lead to high economic loss.
- Conditions
- Primary Prevention, Stress, Tai ji, Adult
- Trial name
- NCT01122706
- Testing
- Taiji training
- Where
- Switzerland
- Volunteers
- 70 people, healthy volunteers welcome
- Sponsor
- University of Bern
Liver Cirrhosis
Effect of Saccharomyces Boulardii in Patients in the Waiting List for Liver Transplant
The purpose of this study is to evaluate the effect of Saccharomyces boulardii in patients in the waiting list for liver transplant.
- Trial name
- NCT01762748
- Testing
- Saccharomyces boulardii
- Where
- Brazil
- Volunteers
- 18 people, healthy volunteers welcome
- Sponsor
- Federal University of Minas Gerais
Occupational Stress, Psychological Stress
Yoga@Work Intervention to Reduce Work-related Stress Among Information Technology Workers
Over the last several decades, occupational stress at workplace comprise a major burden. Office based work are more prone to sedentary lifestyle, postural issues, workplace stress, repetitive strain injury, poor employee health.
- Trial name
- NCT04313517
- Testing
- Yoga
- Where
- 4 sites in Belgium, Hong Kong and 2 more
- Volunteers
- 140 people, healthy volunteers welcome
- Sponsor
- Aarogyam UK
Rotator Cuff Tears
Physiotherapy for Patients Awaiting Rotator Cuff Repair
POWER is a pragmatic multi-centre, external pilot randomised controlled trial with feasibility objectives using a parallel group design with 1:1 allocation ratio and integrated qualitative study.
- Trial name
- POWER (NCT04974242)
- Testing
- Physiotherapist-led exercise
- Where
- United Kingdom
- Volunteers
- 76 people
- Sponsor
- University Hospitals of Derby and Burton NHS Foundation Trust
Intervention 1: Resilience and Coping for Healthcare Group, Intervention 2: Resilience and Coping for Healthcare Plus Additional Services
Health and Wellness in Healthcare Providers Post-disaster
The purpose of this evaluation is to understand the impact of mental health and psychosocial support (MHPS) programming that AmeriCares (a non-profit disaster response organization) is currently providing to healthcare and social…
- Conditions
- Intervention 1: Resilience and Coping for Healthcare Group, Intervention 2: Resilience and Coping for Healthcare Plus Additional Services, Waitlist Control Group
- Trial name
- NCT03722368
- Testing
- RCHC, RCHC+, Waitlist control
- Where
- 2 sites in United States, Puerto Rico
- Volunteers
- 1,100 people, healthy volunteers welcome
- Sponsor
- University of Illinois at Urbana-Champaign
Menthol Cigarettes, Smoking Behavior
DoubleTake: Effect of Message Exposure Via a Discrete Choice Experiment With Eye-Tracking on Quit Attempts Among Adults Who Smoke Menthol Cigarettes
<p>The goal of this clinical trial is to learn how exposure to anti-smoking social media messages affects quitting-related behaviors.
- Conditions
- Menthol Cigarettes, Smoking Behavior, Cigarette Use
- Trial name
- NCT07782879
- Testing
- Message Exposure via Discrete Choice Experiment
- Where
- 2 sites in United States
- Volunteers
- 200 people, healthy volunteers welcome
- Sponsor
- Georgia State University
Aphasia, Acquired
Virtual Reality in Aphasia Telerehabilitation
The main purpose of this study is to evaluate the use of the immersive 3D HMD VR technology in the language intervention with a home-based telerehabilitation approach for people with aphasia.
- Trial name
- NCT04828759
- Testing
- VR-treatment, Treatment as usual
- Volunteers
- 20 people
- Sponsor
- University of Oulu
Chirurgical Intervention
Information Flow of Waiting List for Scheduled Surgical Admissions
Definition and experimentation of the aforementioned information flow within the Regions participating in the three-year project, a Technical Subgroup was identified on a voluntary basis in charge of defining the design and…
- Trial name
- NCT06164886
- Testing
- Waiting list
- Where
- Italy
- Volunteers
- 507 people
- Sponsor
- Istituto Ortopedico Rizzoli
Obstructive Sleep Apnoea (OSA)
A Study Assessing Adult Patients Referred to an NHS Sleep Service With Suspected Obstructive Sleep Apnoea. This Study Aims to Compare the Sunrise Wearable Diagnostic Device Performance and Potential Inclusion in a NHS Diagnostic Pathway With Oximetry and WatchPAT Which Are Currently Used.
The goal of this clinical trial is to evaluate whether the Sunrise device (that measure small jaw movements) can improve the diagnosis and management of Obstructive Sleep Apnoea (OSA) in adults (≥ 18 years) referred to a Sleep…
- Trial name
- SOSA (NCT07269483)
- Testing
- WatchPAT 300, Oximetry, Sunrise
- Where
- United Kingdom
- Volunteers
- 100 people
- Sponsor
- Virginia Hawkins
Happiness in the General Population
Improving Happiness in Flanders
This study aims to assess the effects of two different types of interventions aimed at increasing happiness in the Flemish general population as compared to individuals that receive no intervention.
- Trial name
- HAP-FLA (NCT02041741)
- Testing
- Weekly tips, Daily Tips
- Where
- Belgium
- Volunteers
- 10,863 people, healthy volunteers welcome
- Sponsor
- Universitaire Ziekenhuizen KU Leuven
Achromatopsia
Safety and Efficacy of rAAV.hCNGA3 Gene Therapy in Patients With CNGA3-linked Achromatopsia
The purpose of this study is to proof the safety and efficacy of a single bilateral subretinal injection of rAAV.hCNGA3 in adult and minor patients with CNGA3-linked achromatopsia.
- Trial name
- Colourbridge (NCT02610582)
- Testing
- rAAV.hCNGA3
- Where
- Germany
- Volunteers
- 13 people
- Sponsor
- STZ eyetrial
Migraine
Home-based Biofeedback for the Prevention of Migraine
The goal of this clinical trial is to test an app-based biofeedback treatment in adults with migraine. The aim of the study is to investigate the safety and effectiveness of biofeedback treatment using the medical device Cerebri…
- Trial name
- BioCer (NCT05616741)
- Testing
- Cerebri biofeedback, Cerebri headache diary
- Where
- 4 sites in Norway
- Volunteers
- 279 people
- Sponsor
- Nordic Brain Tech AS
Chronic Lymphocytic Leukemia
HEALTH4CLL2: A Randomized Waitlist Control Trial of Behavioral Interventions in Patients With Chronic Lymphocytic Leukemia
To learn if exercise and weight management can help to improve feelings of fatigue in CLL survivors.
- Trial name
- NCT05879133
- Testing
- Questionnaires, Fit Bit
- Where
- United States
- Volunteers
- 30 people
- Sponsor
- M.D. Anderson Cancer Center
Knee Osteoarthritis
Electroacupuncture Treatment for Those With End Stage Knee Osteoarthritis on a Total Knee Arthroplasty Waitlist
A 3-armed pilot randomized controlled trial: electroacupuncture, sham acupuncture and waitlist groups.
- Trial name
- NCT05374330
- Testing
- Electroacupuncture
- Where
- Canada
- Sponsor
- University of Manitoba
Pedophilia
Prevent It 2.0/PRIORITY - An iCBT to Reduce the Risk of Committing Child Sexual Abuse
Child sexual exploitation and abuse is a large-scale global issue that has been drastically rising since the advent of the internet that has brought about communication technologies enabling new ways to sexually abuse children.
- Trial name
- NCT05831657
- Testing
- Prevent It 2.0, Waitlist
- Where
- 3 sites in Germany, Portugal and 1 more
- Volunteers
- 205 people
- Sponsor
- Karolinska Institutet
Obsessive Compulsive Disorder
Wait-list Study of One-Week Intensive Cognitive-Behavioral Therapy for Pediatric Obsessive-Compulsive Disorder (OCD)
The purpose of this study is to examine how well intensive cognitive-behavioral therapy (CBT) delivered over 5 days works in reducing Obsessive-Compulsive Disorder (OCD) symptoms in children and adolescents.
- Trial name
- 5dayOCD (NCT01194076)
- Testing
- 5-day intensive treatment
- Where
- 3 sites in United States
- Volunteers
- 28 people
- Sponsor
- Mayo Clinic