Clinical trials: For Intervention
Cervical Pain, Pain, Radiating
Neck-specific Training or Prescribed Physical Activity for Patients With Cervical Radiculopathy
The overall objective is to evaluate if treatment with a neck-specific exercise program and cognitive behavioural approach improves the outcome compared with prescribed, self-mediated and progressive physical activity in patients…
- Trial name
- NCT01831271
- Testing
- Prescribed physical activity, Neck specific training
- Where
- Sweden
- Volunteers
- 144 people
- Sponsor
- Karolinska University Hospital
Breast Cancer
Decisional Aid Intervention for Women Considering Breast Reconstruction
This is an intervention development and pilot study whose purpose is to determine the feasibility and acceptability of the breast reconstruction decisional aid (BRDA) and provide preliminary data on its impact on decisional…
- Trial name
- BRDA (NCT01951534)
- Testing
- Breast Reconstruction Decisional Aid (BRDA), Usual Care
- Where
- 9 sites in United States
- Volunteers
- 56 people
- Sponsor
- Rutgers, The State University of New Jersey
Cardiac Surgery, Surgical Stress Response
Guided Visualization Meditation for Reducing Surgical Stress Response in Cardiac Surgery Patients
This study aims to evaluate whether guided visualization meditation can reduce the surgical stress response in patients undergoing open-heart surgery.
- Conditions
- Cardiac Surgery, Surgical Stress Response, Coronary Artery Disease, Postoperative Stress
- Trial name
- GVM-CARDIO (NCT07379944)
- Testing
- Guided Visualization Meditation
- Where
- Turkey (Türkiye)
- Volunteers
- 72 people
- Sponsor
- University of Gaziantep
CNLDO - Congenital Nasolacrimal Duct Obstruction, Amblyopia
Improving the Follow up Rate for Pediatric Patients
Follow-up of pediatric patients is important for their regular ocular morbidity monitoring, especially for amblyopia management.
- Conditions
- CNLDO - Congenital Nasolacrimal Duct Obstruction, Amblyopia, Conjunctivitis, Eye Injuries
- Trial name
- NCT04837534
- Testing
- Counseling group, SMS and phone call reminder group
- Where
- Nepal
- Volunteers
- 264 people
- Sponsor
- Seva Foundation
Lung Cancer
CT-controlled Advanced Navigation Techniques for Transbronchial Pulmonary Lesion Access; Evaluation of Augmented Fluoroscopy Bronchoscopic Navigation Based Diagnostic Yield
In this exploratory adaptive clinical trial the investigators will examine the diagnostic yield of a combination of commercially available imaging and navigation techniques for reaching peripheral lung lesions.
- Trial name
- CONTROL-A (NCT03274609)
- Testing
- Augmented fluoroscopy
- Where
- Netherlands
- Volunteers
- 47 people
- Sponsor
- Radboud University Medical Center
Melanoma (Skin), Metastatic Melanoma
A Prospective Observational Study on Targeted Therapy for Unresectable or Metastatic BRAFV600E Mutant Melanoma Patients
1. Background The purpose of this study is to describe the profile of patients with BRAF-mutated melanoma treated with BRAF/MEK inhibitors combination and using the Tavie Skin application.
- Conditions
- Melanoma (Skin), Metastatic Melanoma, BRAF V600 Mutation
- Trial name
- TavieSkin (NCT04911998)
- Where
- Portugal
- Volunteers
- 400 people
- Sponsor
- Pierre Fabre Medicament
HIV
Intervention for Newly Diagnosed Youth With HIV
This study will pilot test an HIV intervention for newly diagnosed youth (diagnosed for less than 15 months) to assess its acceptability and feasibility preliminary to and leading up to a full-scale, randomized trial.
- Trial name
- NCT00510237
- Testing
- "Adolescents Coping, Connecting, Empowering, and Protecting Together" (Project ACCEPT)
- Where
- 4 sites in United States
- Volunteers
- 50 people
- Sponsor
- University of North Carolina, Chapel Hill
Stroke
Feasibility Randomised-Controlled Trial of Online Stroke Interventions
Many people have difficulties organising their behaviour and problem-solving (also known as executive function difficulties) after stroke.
- Trial name
- NCT05461937
- Testing
- Getting things done after stroke, Stroke psychoeducation
- Where
- United Kingdom
- Volunteers
- 22 people
- Sponsor
- University of East Anglia
Readmission
Individual Nutritional Intervention for the Prevention of Readmission Among Geriatric Patients
The purpose of this study is to investigate whether a four-week individual nutritional intervention can reduce the readmission/hospitalization rate among geriatric patients who are discharged to their private home or respite…
- Trial name
- NCT03519139
- Testing
- individual dietary counselling
- Where
- Denmark
- Volunteers
- 40 people
- Sponsor
- Jens Rikardt Andersen
Psychotic Disorders
Optimal Duration of Early Intervention for Psychosis
A total of 160 subjects, who aged 18-35 and had completed the first 2 years of case management in the EASY programme will be randomized in 1:1 ratio into either (1) receiving an additional year of case management, or (2)…
- Trial name
- NCT01202357
- Testing
- Community Case Management
- Where
- China
- Volunteers
- 160 people
- Sponsor
- The University of Hong Kong
Insomnia, Insomnia Chronic
SHADES Mechanistic Trial
Cardiovascular disease (CVD) is common, deadly, and costly, and adults with insomnia represent a large group of people at elevated risk of developing CVD in the future.
- Conditions
- Insomnia, Insomnia Chronic, Insomnia, Primary, Sleep Disturbance
- Trial name
- SHADES (NCT06041581)
- Testing
- Sleep Healthy Using The Internet (SHUTi), Telephonic CBT-I, Face-to-Face CBT-I
- Where
- United States
- Volunteers
- 200 people
- Sponsor
- Indiana University
Coronary Angioplasty, Coronary Artery Disease
Arterial Closure vs Direct Compression for Hemostasis After PCI - The ACDC Trial
Hemostasis at the arterial puncture site after percutaneous coronary interventions is achieved by either placement of a puncture closure device or by delaying sheath removal for hours to allow normalization of heparin induced…
- Trial name
- NCT00264264
- Testing
- Closure Device, Direct Compression
- Where
- Canada
- Volunteers
- 572 people
- Sponsor
- Unity Health Toronto
Iatrogenic ASD, Mitral Regurgitation
Iatrogenic Atrial Septal Defect Gradient for Intraprocedural Success After M-teer
Transcatheter mitral edge-to-edge repair (M-TEER) has become an established minimally invasive therapy for patients with severe mitral regurgitation (MR) who are at high or prohibitive surgical risk.
- Trial name
- IASIS (NCT07798037)
- Testing
- M-TEER
- Where
- Greece
- Volunteers
- 100 people
- Sponsor
- Hippocration General Hospital
Ischemic Heart Disease, Stenotic Coronary Lesion
RESOLUTE ONYX China Single Arm Study
It is a single arm clinical evaluation of safety and efficacy of the Medtronic Resolute Onyx™ zotarolimus-eluting coronary stent system in subjects who are eligible for percutaneous transluminal coronary angioplasty (PTCA) in de…
- Conditions
- Ischemic Heart Disease, Stenotic Coronary Lesion, Cardiovascular Diseases, Arteriosclerosis
- Trial name
- NCT03471845
- Testing
- Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System
- Where
- China
- Volunteers
- 591 people
- Sponsor
- Medtronic Vascular
Psychological Distress, Stress, Psychological
ASD (Autism Spectrum Disorder) Telehealth for Distress Related to COVID-19
The purpose of this study is to evaluate the feasibility, acceptability and effectiveness of a brief, telehealth intervention (the Emotional Support Plan), intended to support autistic adults to cope with their negative emotions…
- Conditions
- Psychological Distress, Stress, Psychological, Autism Spectrum Disorder
- Trial name
- NCT04460677
- Testing
- Emotional Support Plan, Daily Monitoring
- Where
- United States
- Volunteers
- 26 people
- Sponsor
- Rutgers, The State University of New Jersey
Posttraumatic Stress Disorder (PTSD), Specific Phobia
Intervention for Anxiety After Falls
The purpose of this study is to determine whether a brief intervention for disabling anxiety is practical to conduct and beneficial for older adults injured by falls.
- Conditions
- Posttraumatic Stress Disorder (PTSD), Specific Phobia, Anxiety
- Trial name
- NCT01268657
- Testing
- Education, Relaxation Training, Cognitive Restructuring
- Where
- United States
- Volunteers
- 23 people
- Sponsor
- Weill Medical College of Cornell University
Neoplasms
Feasibility of an Advance Care Planning Intervention
Advanced Cancer patients hospitalized in a Cancer center inpatient unit have a dismal prognosis. Palliative Care interventions have shown multiple benefit for those patients, regarding quality of life, symptom management, illness…
- Trial name
- PREVOIR (NCT06149312)
- Testing
- Advance Care Planning Intervention
- Where
- France
- Volunteers
- 120 people
- Sponsor
- Institut de cancérologie Strasbourg Europe
Acne Vulgaris, Medical Education
AI-Generated Acne Vulgaris Learning Material Study
This comparative educational intervention study evaluated the educational effectiveness of artificial intelligence-generated patient information material on acne vulgaris among early-year medical students.
- Trial name
- NCT07652112
- Testing
- Artificial Intelligence-Generated Acne Vulgaris Educational Material, Turkish Dermatology Association Acne Vulgaris Educational Material
- Where
- Turkey (Türkiye)
- Volunteers
- 190 people, healthy volunteers welcome
- Sponsor
- Hasan Durmuş
Smoking Cessation
COVID-19 Brief Advice and Chat-based Support for Smoking Cessation Via "Quit to Win" Contest 2020
The present study will examine (1) the effectiveness of a combined brief advice and personalized chat-based support on COVID-19 related smoking messages and (2) explore the use of CBPR model to build capacity and to engage…
- Trial name
- QTW2020 (NCT04399967)
- Testing
- Chat-based support, AWARD plus COVID-specific advice, AWARD advice
- Where
- China
- Volunteers
- 1,166 people
- Sponsor
- The University of Hong Kong
Psychomotor Agitation
Four Interventions in the Management of Psychomotor Agitation, Safety and Efficacy Evaluation
This study aims to evaluate the efficacy and safety of four options of medications in the management of acute psychomotor agitation,or violence and aggression situations in health services.
- Trial name
- NCT01485692
- Testing
- haloperidol+promethazine, haloperidol + midazolam, olanzapine
- Where
- Brazil
- Volunteers
- 120 people
- Sponsor
- University of Sao Paulo
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