Clinical trials: Intervention Effectiveness
Prostatic Neoplasms, Castration-Resistant
Non-interventional Study With Ra-223 Dichloride Assessing Overall Survival and Effectiveness Predictors for mCRPC Patients in a Real Life Setting in Germany
This observational prospective single arm cohort study is designed to assess overall survival, symptomatic skeletal event free survival and quality of life of metastatic Castration Resistant Prostate Cancer (mCRPC) patients…
- Trial name
- URANIS (NCT02450812)
- Testing
- Radium-223-dichloride (Xofigo, BAY88-8223)
- Where
- Germany
- Volunteers
- 86 people
- Sponsor
- Bayer
Postmenopause
Effects of Wellnara on Climacteric Symptoms
Aim of this NIS is to obtain further information on efficacy, tolerability, and acceptance of Wellnara in a large user population under the conditions of routine medical practice.
- Trial name
- NCT00913926
- Testing
- E2/LNG oral (Wellnara, BAY86-5029)
- Where
- Germany
- Volunteers
- 749 people
- Sponsor
- Bayer
Movement Disorders
Effectiveness of Vojta Therapy in Motor Development of Preterm Children
Justification: Prematurely born children have an increased prevalence of neurodevelopment problems in the first two years. Knowledge regarding the effects of early intervention programs is essential to the follow up of these…
- Trial name
- NCT01838278
- Testing
- Vojta Physiotherapy Method
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Universidad de Murcia
Post Traumatic Stress Disorder
Assessment of a Brief Post Traumatic Stress Disorder Intervention for Use in Botswana
The purpose of this study is to culturally adapt a brief psychological intervention for Post-Traumatic Stress Disorder (PTSD) and assess its efficacy, feasibility, and acceptability in a pilot trial.
- Trial name
- NCT04426448
- Testing
- Brief Relaxation, Education And Trauma HEaling
- Where
- Botswana
- Volunteers
- 36 people
- Sponsor
- University of Botswana
Crohn's Disease
Efficacy of CROWN in Repair and Maintenance of the Intestinal Mucosa in Patients With CD Receiving Anti-TNF Therapy
The purpose of this study is to evaluate CROWN's efficacy in supporting the repair and maintenance of the intestinal mucosa of patients with moderately to severely active Crohn's Disease receiving anti-Tumor Necrosis Factor (TNF)…
- Trial name
- PIONEER-CD (NCT02793778)
- Testing
- CROWN
- Where
- 39 sites in United States
- Volunteers
- 42 people
- Sponsor
- Prometheus Laboratories
Neonatal Care
Mobile Health Intervention to Improve Neonatal Care Practice
Effectiveness of interactive mobile health intervention (IMHI) to improve neonatal care practice among postpartum women in Dessie and Kombolcha town zones, north east Ethiopia: behavioral cluster randomized control trial.
- Trial name
- NCP (NCT05666050)
- Testing
- Mobile health intervention
- Where
- Ethiopia
- Volunteers
- 784 people, healthy volunteers welcome
- Sponsor
- Wollo University
Inflammatory Bowel Diseases
A Multimodal Wearable Device-based Study to Evaluate the Efficacy of an Exercise Prescription Intervention in IBD
This project is a multimodal wearable device-based evaluation of the efficacy of an exercise prescription intervention for inflammatory bowel disease in a This is a single-center, randomized controlled clinical study to evaluate…
- Trial name
- NCT06427135
- Testing
- Exercise interventions
- Volunteers
- 56 people
- Sponsor
- Ping An
Sedentary Lifestyle
RCT Computer-tailored Intervention on Workplace Sitting
A theory-driven, web-based, computer-tailored advice to influence sitting at work was developed. The study investigated the effects of this computer-tailored intervention to influence workplace sitting on behavioural measures.
- Trial name
- StartToStand (NCT02672215)
- Testing
- Start to stand, generic advice
- Volunteers
- 1,061 people
- Sponsor
- University Ghent
Autism Spectrum Disorder
Examining the Efficacy of a Mobile Therapy for Children With Autism Spectrum Disorder
The purpose of this research is to study the effects of a novel artificial intelligence (AI) tool for automatic facial expression recognition that runs on Google Glass through an Android app to deliver social emotion cues to…
- Trial name
- NCT03569176
- Testing
- Autism Glass
- Volunteers
- 74 people
- Sponsor
- Dennis Paul Wall
Test Anxiety
Effectiveness of Cognitive Behavioral Therapy of Reduction of Test Anxiety
This study will evaluate the role of Group Cognitive Behavioral Therapy in test anxiety. The study participants will be psychology undergraduates with social work and psychology majors.
- Trial name
- GroupCBT (NCT04500340)
- Testing
- Group CBT for test anxiety
- Where
- Nepal
- Volunteers
- 80 people, healthy volunteers welcome
- Sponsor
- University Grants Commission
Water Consumption, Healthy Lifestyle
Effectiveness of the Numerous Educational Strategy Interventions Seeking to Increase the Water Consume in Child
The current project seeks to evaluate the effectiveness of numerous educational strategy interventions to increase the percentage of water consumed among early elementary school students over a 1-year period.
- Conditions
- Water Consumption, Healthy Lifestyle, Elementary School
- Trial name
- ECCA001LCE (NCT03254615)
- Testing
- "I Prefer Plain Water"
- Where
- Mexico
- Volunteers
- 329 people, healthy volunteers welcome
- Sponsor
- Jose Francisco Gonzalez-Zamora
Asthma Intermittent, Uncontrolled
Εffectiveness of a Digital Social Intervention in Primary Care
The goal of this study is to deliver a definitive randomised controlled trial to measure the effectiveness and assess cost-effectiveness of a digital social intervention for patients with asthma, composed of promoting engagement…
- Trial name
- ADHOC (NCT06849245)
- Testing
- A digital social intervention by primary care clinicians
- Where
- 5 sites in United Kingdom
- Volunteers
- 600 people
- Sponsor
- Queen Mary University of London
Prostate Neoplasm, Prostatectomy
Efficacy of Extracorporeal Biofeedback Device for Post-prostatectomy Incontinence
To evaluate the efficacy of postoperative pelvic floor muscle training using personalized extracorporeal biofeedback device among patients with post-prostatectomy incontinence
- Conditions
- Prostate Neoplasm, Prostatectomy, Surgical Procedures, Robotic, Urinary Incontinence
- Trial name
- NCT02485665
- Testing
- Extracorporeal biofeedback device (Any Kegel)
- Where
- South Korea
- Volunteers
- 84 people
- Sponsor
- Seoul National University Hospital
Cleft Lip and Palate, Growth and Development
Efficacy of Maxillo-facial Treatment on Cleft Lip and Palate Patients Faces: Aesthetic Considerations
The aim of the study is to analyze the esthetic outcome of the first surgical repair of cleft lip and palate (CLP) patients. The aim of the study is to identify differences in the aesthetic evaluation of full-face and nasolabial…
- Conditions
- Cleft Lip and Palate, Growth and Development, Cicatrix, Randomized Controlled Trial
- Trial name
- NCT03395015
- Testing
- VAS scale (from 1 to 10) esthetic assessment of facial 3-D images
- Where
- Italy
- Volunteers
- 10 people
- Sponsor
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS
HIV
Switching From Protease Inhibitor (PI) to Etravirine in HIV-1 Infected Subjects With Viremia Suppression
This is a 48 week randomized, prospective, controlled, open-label, proof-of-concept pilot clinical trial. Patients with HIV-1 infection on HAART PI-based regimen will be randomized to switch from the PI to etravirine (400 mg…
- Trial name
- NCT01034917
- Testing
- Etravirine 400 mg dissolved in water every 24 hours, Continue with the same antiretroviral regimen
- Where
- Spain
- Volunteers
- 43 people
- Sponsor
- Germans Trias i Pujol Hospital
Feeding and Eating Disorders
Intervention Program to Improve Body Image and Self-Esteem Among Female Athletes.
A controlled, randomized clinical intervention study which includes the development and activation of an intervention program designed to prevent eating disorders among adolescent female aesthetic athletes.
- Trial name
- NCT03211468
- Testing
- Clinical intervention program to prevent eating disorders
- Where
- Israel
- Volunteers
- 95 people, healthy volunteers welcome
- Sponsor
- Tel Hai College
Clostridium Difficile Infection-associated Diarrhea and Colitis
Efficacy and Safety of Teicoplanin in CDAD
Primary Objective: Explore the efficacy of teicoplanin (100-200 mg administered orally twice a day for 7 to 14 days) in patients with Clostridium difficile infection-associated diarrhea and colitis Secondary Objective: Evaluate…
- Trial name
- NCT04003818
- Testing
- TEICOPLANIN
- Where
- China
- Volunteers
- 50 people
- Sponsor
- Sanofi
Opioid-Related Disorders, Drug Overdose
Repeated-dose Behavioral Intervention to Reduce Opioid Overdose
REBOOT is a randomized trial of a repeated-dose brief intervention to reduce overdose and risk behaviors among naloxone recipients with opioid use disorder.
- Trial name
- REBOOT (NCT03838510)
- Testing
- REBOOT
- Where
- 2 sites in United States
- Volunteers
- 268 people
- Sponsor
- San Francisco Department of Public Health
Pancreatic Neuroendocrine Tumors
The Safety And Efficacy Of Sunitinib In Chinese Patients With Progressive Advanced Or Metastatic Well-Differentiated Unresectable Pancreatic Neuroendocrine Tumors
This study is a multi-center, prospective, non-interventional (NI) study evaluating the safety and efficacy of sunitinib in Chinese patients with progressive, unresectable, advanced or metastatic well-differentiated, pancreatic…
- Trial name
- NCT02282059
- Testing
- sunitinib
- Where
- 24 sites in China
- Volunteers
- 100 people
- Sponsor
- Pfizer
Smoking, Smoking Behaviors
Take A Break - Rural
The study team proposes a multi-level trial to test 1) novel implementation programs in rural counties designed to increase access to 2) recent advances in tobacco control services for people who are not-yet-ready-to-quit…
- Conditions
- Smoking, Smoking Behaviors, Smoking Cessation
- Trial name
- TABR (NCT05790486)
- Testing
- Take a Break plus Nicotine replacement therapy (NRT) Sampling, The Comparison, Community Paramedicine Standard Plus Enhanced Implementation Program
- Where
- United States
- Volunteers
- 800 people, healthy volunteers welcome
- Sponsor
- Wake Forest University Health Sciences
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