Clinical trials: Interventional Study
Pregnant Women
Adapted Physical Activity to Promote Quality of Life, Well-being and Physical Activity Levels in Pregnant Women (WELL-DONE!Study)
The aim of the WELL-DONE! Study is to co-design, using different professional figures (midwives, psychologists, master's degree in motor science) but also taking into consideration the pregnant women's point of view, an…
- Trial name
- WELL-DONE! (NCT04735146)
- Testing
- Adapted physical activity
- Where
- Italy
- Volunteers
- 150 people, healthy volunteers welcome
- Sponsor
- First Cycle Degree in Midwifery in collaboration with the Department of Biomedical and Neuromotor Sc
Physical Activity, Obesity
Effectiveness of a Physical Activity Intervention on the Obesity of Schoolchildren
The purpose of this study is to evaluate the effectiveness of a recreational physical activity intervention (RPAI) for reducing the prevalence of overweight/obesity and other cardiovascular risk factors
- Conditions
- Physical Activity, Obesity, Children
- Trial name
- Movi2 (NCT01277224)
- Testing
- Movi2 Program
- Volunteers
- 1,200 people, healthy volunteers welcome
- Sponsor
- University of Castilla-La Mancha
Smoking
Adult Follow-up of Preventive Study With Brief Smoking Intervention for Adolescents
The purpose of this study was to see whether a brief intervention given in adolescence has an effect on smoking in adulthood. The investigators also wanted to clarify the significance of some known psychosocial risk factors of…
- Trial name
- TuNAMI (NCT01348646)
- Testing
- Brief intervention
- Where
- Finland
- Volunteers
- 2,582 people
- Sponsor
- Tampere University Hospital
Endometrial Carcinoma, Endometrial Carcinoma Stage III
GYNORYLAQ™-VLINIVAL™: Ψ-Guided Personalized Neoantigen Peptide Vaccine for High-Risk Endometrial Cancer
GYNORYLAQ-VLINIVAL is an Early Phase I, non-randomized, single-arm, open-label clinical trial enrolling 40 patients with high-risk or recurrent endometrial carcinoma.
- Trial name
- GYNORYLAQ™ (NCT07316361)
- Testing
- • Biological: GYNORYLAQ-TM Personalized Neoantigenic Peptide Vaccine
- Where
- Greece
- Volunteers
- 40 people
- Sponsor
- Biogenea Pharmaceuticals Ltd.
Ocular Discharge
PMCF Study to Evaluate Performance and Safety of "LUXIDROPIN BABY & JUNIOR"
Children's tear film and ocular surface are increasingly exposed to environmental factors. The tear film is the most important barrier protecting the eye from external insults such as pollen, dust, sand.
- Trial name
- NCT05855486
- Testing
- Saline eye drops
- Where
- Italy
- Volunteers
- 32 people
- Sponsor
- C.O.C. Farmaceutici S.r.l.
Child, Only, Narration
Effects of a Group EMDR Intervention on Narrative Complexity and Specificity of Autobiographical Memories: the Hug the Child Study (HTC)
Background and study aims: The Eye Movement Desensitization and Reprocessing Group Protocol with Children (EMDR-GP/C) was first developed by Korkmazlar following the Marmara earthquake in Turkey in 1999 and can be adapted for…
- Conditions
- Child, Only, Narration, Memory Dysfunction, Distress, Emotional
- Trial name
- HTC (NCT05319002)
- Testing
- Group EMDR
- Where
- Italy
- Volunteers
- 27 people, healthy volunteers welcome
- Sponsor
- University of Pisa
Fever, Sepsis
AION BIOSYSTEMS, INC. Tempshield for Continuous Tempreature Monitoring
The purpose of this research study is to evaluate the effectiveness of the AION BIOSYTEMS, INC. tempshield ("Shield") temperature monitoring device and platform in detecting body temperature for children 2-4 years old.
- Trial name
- NCT07145541
- Testing
- Aion Tempshield Device
- Where
- United States
- Volunteers
- 72 people
- Sponsor
- AION Biosystems
Sleep Disturbance, Asthma
Sleep Intervention for Kids and Parents: A Self-Management Pilot Study
Behavioral intervention for 6-11 year children with persistent asthma and sleep disturbance and a parent with sleep disturbance.
- Trial name
- SKIP (NCT03144531)
- Testing
- Sleep Intervention for Kids and Parents (SKIP)
- Where
- United States
- Volunteers
- 66 people
- Sponsor
- University of Washington
Clinical Research, Cancer
Study Evaluating Intervention in the Development of Clinical Research in Non-Academic Health Institution (ERNU)
This study evaluates the interventions of the Cancéropôle Nord-Ouest in the development of clinical research in non-academic health institution. The randomization, in open label,determines the duration of the interventions.
- Trial name
- ERNU (NCT02765451)
- Testing
- interventions of the Cancéropôle Nord-Ouest
- Where
- 41 sites in France
- Volunteers
- 40 people
- Sponsor
- Centre Hospitalier Universitaire, Amiens
Hepatitis B
Tenofovir in Early Pregnancy to Prevent Mother-to-child Transmission of Hepatitis B Virus
Mother-to-child transmission (MTCT) of hepatitis B virus (HBV) remains the major mode of transmission in most high and intermediate HBV endemic areas, despite existing WHO immunoprophylaxis recommendations.
- Trial name
- NCT02995005
- Testing
- Tenofovir Disoproxil Fumarate
- Where
- Thailand
- Volunteers
- 98 people
- Sponsor
- Johns Hopkins Bloomberg School of Public Health
Child Development
KeySteps@JC Phase One Follow-up Study
This proposed study is a 5-year follow-up study of "KeySteps Phase One Study", which focused on bridging the gap between students from privileged and underprivileged families.
- Trial name
- NCT05778669
- Testing
- Monitoring of medical, health and psychosocial conditions
- Where
- Hong Kong
- Volunteers
- 1,486 people, healthy volunteers welcome
- Sponsor
- The University of Hong Kong
Disaster Planning, Emergency Medical Services
The KAEPacity Study Analyzes Hospital Emergency and Disaster Plans From Hospitals Across Germany to Evaluate How Well Hospitals Are Prepared for Crises and Disasters Organizational Structures Communication Leadership Training Are Examined Within These Plans No Medical Intervention is Performed
Hospital Emergency and Disaster Plans (Krankenhausalarm- und Einsatzplan-KAEP) are a central component of hospital preparedness in Germany.
- Conditions
- Disaster Planning, Emergency Medical Services, Germany
- Trial name
- KAEPacity (NCT07440329)
- Where
- Germany
- Volunteers
- 319 people
- Sponsor
- Lea Kölsch
Obesity
Efficacy of Motivational Interview in the Treatment of Obesity and Overweight in Adolescents
The objective of the study is to investigate the efficacy of motivational interview intervention with adolescent students at a school environment on the adhesion to a therapeutic plan to loose weight.
- Trial name
- IMAGINE (NCT02745795)
- Testing
- Motivational Interview, Conventional Interview
- Volunteers
- 83 people, healthy volunteers welcome
- Sponsor
- Centro Hospitalar Lisboa Norte
Apnea of Newborn, Hypoxia Neonatal
A UK Interventional Trial in Premature Infants With Apnea of Prematurity Using a Simple, Non-invasive Vibratory Device to Study the Effectiveness in Supporting Breathing and General Stability
Purpose of Study: Apnoea of Prematurity (AOP) is common, affecting the majority of infants born <34 weeks gestational age (GA). Apnea is accompanied by intermittent hypoxia (IH), which contributes to multiple pathologies…
- Conditions
- Apnea of Newborn, Hypoxia Neonatal, Bradycardia Neonatal
- Trial name
- WAVE (NCT04528030)
- Testing
- WAVE device
- Volunteers
- 17 people
- Sponsor
- Inspiration Healthcare
Atopic Dermatitis
Abrocitinib Treatment of Atopic Dermatitis in Children 2 to Less Than 6 Years of Age
This clinical study is designed to test how well a medicine called abrocitinib works and how safe it is for young children (ages 2 to under 6) who have moderate-to-severe eczema (also known as atopic dermatitis).Eczema is a skin…
- Trial name
- NCT07823595
- Testing
- Abrocitinib
- Volunteers
- 90 people
- Sponsor
- Pfizer
Cancer Patients
The Risk Factors for Acute Radiation Pneumonitis in Patients With Prior Receipt of Immune Checkpoint Inhibitors
The purpose of this non-interventional study is to collect data on the risk factors for acute radiation pneumonitis in patients with prior receipt of immune checkpoint inhibitors.
- Trial name
- NCT05219851
- Testing
- Cancer patients underwent thoracic intensity-modulated radiotherapy
- Where
- China
- Volunteers
- 250 people
- Sponsor
- Hubei Cancer Hospital
Palliative Care
Acupuncture Intervention for AYA With Cancer
The aim of the study is to innovatively extend acupuncture research in adult oncology to adolescents and young adults (AYA) by piloting a tailored acupuncture protocol for pain management in AYA in the Children's Hospital of…
- Trial name
- NCT03516799
- Testing
- Acupuncture
- Where
- United States
- Volunteers
- 55 people
- Sponsor
- Children's Hospital of Philadelphia
Anemia
Study to Evaluate the Efficacy & Safety of the INTERCEPT Blood System for RBCs in Complex Cardiac Surgery Patients
The objective of this study is to evaluate the efficacy and safety of RBC transfusion for support of acute anemia in cardiovascular surgery patients based on the clinical outcome of renal impairment following transfusion of red…
- Trial name
- ReCePI (NCT03459287)
- Testing
- INTERCEPT, Control
- Where
- 18 sites in United States
- Volunteers
- 581 people
- Sponsor
- Cerus Corporation
Bipolar Disorder, Bipolar I Disorder
A Non-Interventional Pilot Study to Explore the Role of Gut Flora in Bipolar Disorder
This study seeks to correlate microbiome sequencing data with information provided by patients and their medical records.
- Conditions
- Bipolar Disorder, Bipolar I Disorder, Bipolar II Disorder, Bipolar Type I Disorder
- Trial name
- NCT04211428
- Testing
- No intervention
- Where
- United States
- Sponsor
- ProgenaBiome
Hemophilia A, Congenital
Alphanate in Immune Tolerance Induction Therapy
This is a multicenter, multinational, prospective, single-arm, nonrandomized, open-label study, planned in of approximately 25 male participants with congenital hemophilia A who will receive their first (primary) immune tolerance…
- Trial name
- NCT03095287
- Testing
- Alphanate
- Where
- 20 sites in United States, Canada and 4 more
- Volunteers
- 2 people
- Sponsor
- Grifols Therapeutics LLC
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