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Child Safety Seat

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1121. Evaluation of Smokefree England: a longitudinal, qualitative study

of ‘passive exposure’ It was generally believed that babies and young children are more vulnerable to tobacco smoke than adults, but this was coupled with a view among some participants that children cannot be protected from exposure as they become more mobile. The extent and ways in which smokers, non-smokers and key stakeholders seek to anticipate/accommodate to the impending legislation There was a general sense of optimism about the impact of the legislation in advance, especially among younger (...) characteristics. · Some groups within the population appeared to be more affected than others: o Those living in the more disadvantaged localities were less likely than smokers in the more affluent areas to have access to more comfortable outdoor spaces o In areas of disadvantage, some older men and women with children curtailed social activities and experienced a sense of loss of the pleasures of socialising in bars and cafés where they could smoke with friends o South Asian men reported that it could

2009 Public Health Research Consortium

1122. Toddler Overweight Prevention Study Among Low-Income Families

and engage in physical activity than toddlers with parents in a placebo (safety) intervention. Condition or disease Intervention/treatment Phase Overweight Obesity Depression Behavioral: Maternal Physical Activity and Nutrition Behavioral: Parenting Behavioral: Child Safety Not Applicable Detailed Description: Background: Overweight is a serious public health problem which can begin in early childhood. Factors which contribute to overweight include: overfeeding, excessive intakes of fat and sugar (...) focusing on healthy diet and physical activity patterns for mothers; 2) a toddler parenting intervention focusing on parenting, limit setting, and development strategies; and 3) an intervention on child safety. The interventions are implemented over 3 months, with 8 sessions. The investigators hypothesize that altering maternal behavior will have a positive impact on the growth and development of the toddler by preventing behaviors that lead to overweight among children. The parenting intervention

2013 Clinical Trials

1123. GSK2339345 Hypertussive Challenge Study

GSK2339345 Hypertussive Challenge Study GSK2339345 Hypertussive Challenge Study - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. GSK2339345 Hypertussive Challenge Study The safety and scientific validity (...) for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 16 participants Allocation: Randomized Intervention Model: Crossover Assignment Masking: Double (Participant, Investigator) Primary Purpose: Treatment Official Title: A Randomised, Double-Blind (Sponsor-Unblind), Placebo Controlled, Cross-Over Study to Investigate the Efficacy, Effect on Cough Reflex Sensitivity, Safety, Tolerability and Pharmacokinetics of Inhaled GSK2339345 in Patients With Chronic Idiopathic Cough

2013 Clinical Trials

1124. A Clinical and Molecular Risk-Directed Therapy for Newly Diagnosed Medulloblastoma

with medulloblastoma. Multivariable general linear mixed models will be used to look for associations between sleep quality as measured by Actigraph accelerometer and a sleep diary with measures of cognitive performance (memory, attention and executive function (detailed above) and internalizing and externalizing behavior. Internalizing and externalizing behaviors will be measured using the Behavior Assessment System for Children, 2nd Edition (BASC-2). There are Preschool, Child and Adolescent versions (...) period and at home, prior to the start of chemotherapy, on hand grip strength as measured using a hand-held dynamometer among children treated for medulloblastoma. Participants will be seated with the shoulder at 0-10 degrees and the elbow in 90 degrees of flexion. The forearm will be positioned in neutral. Each participant will complete three trials, the average used for analysis. Change in range of motion [ Time Frame: Baseline (at enrollment), 12 weeks, at end of adjuvant chemotherapy (28 weeks

2013 Clinical Trials

1125. Virtual Reality Therapy and Imaging in Combat Veterans With Blast Injury and Posttraumatic Stress Disorder

). Please remove one or more studies before adding more. Virtual Reality Therapy and Imaging in Combat Veterans With Blast Injury and Posttraumatic Stress Disorder (ViRTICo-BP) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT01990547 Recruitment Status : Completed First Posted : November 21, 2013 Last (...) under control with treatment will be included. Specific criteria according to arm: Healthy OIF/OEF veterans who deployed for at least 3 months in support of OIF/OEF who do not have blast exposure (i.e., within 100 feet of a blast, in which the pressure wave knocked them to the ground or caused other physical symptoms, or the vehicle in which they were riding hit an improvised explosive device, jarring them from their seat) or PTSD: PCL-M<50, negative history of concussion or loss of consciousness

2013 Clinical Trials

1126. Combined Modality Treatment of Sarcomas of the Extremities

of the Extremities (PASART-1) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT01985295 Recruitment Status : Completed First Posted : November 15, 2013 Last Update Posted : October 9, 2015 Sponsor: The Netherlands Cancer Institute Collaborator: GlaxoSmithKline Information provided by (Responsible Party (...) at 400mg daily, orally in combination with the standard 25 x 2Gy preoperative radiotherapy in newly diagnosed extremity sarcoma patients. Dose of pazopanib will be escalated via 600mg to maximally 800mg. Overall treatment time of pazopanib is 40 days. Other Name: Compound Number: GW786034 Outcome Measures Go to Primary Outcome Measures : Dose limiting toxicity [ Time Frame: 14 weeks ] To study the safety and feasibility of adding 6 weeks of orally administered Pazopanib to 25 x 2Gy in 5 weeks

2013 Clinical Trials

1127. The Effects of Combined Exercise Training on Exercise Capacity in Cardiac Rehabilitation

before adding more. The Effects of Combined Exercise Training on Exercise Capacity in Cardiac Rehabilitation (DOPPELHERZ) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT01921036 Recruitment Status : Completed First Posted : August 13, 2013 Last Update Posted : January 26, 2015 Sponsor: Technische (...) . Individualized combined exercise (ICE): The ICE group participated in once-weekly individualized combined resistance-endurance exercise training for 60 minutes and once-weekly traditional group-based cardiac rehabilitation as described above. The ICE intervention included 30 minutes of endurance exercise at 60-70% VO2peak and RPE 11-14 and five resistance exercises (chest press, leg press, lat pull-downs, shoulder press and seated cable row) following the recommendations of the German Federation

2013 Clinical Trials

1128. Improving Signout Accuracy and Information Delivery in the Emergency Department

. Improving Signout Accuracy and Information Delivery in the Emergency Department (SAID-ED) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT01859286 Recruitment Status : Completed First Posted : May 21, 2013 Last Update Posted : May 21, 2013 Sponsor: The University of Texas Health Science Center, Houston (...) to Group/Cohort Intervention/treatment regular sign out process Other: standardized sign out process The intervention phase included was the introduction of a standardized TOC (transfer of care) process, which occurred during April and May of 2012. TOC was done at a predefined location in each section of the emergency department (Medicine and Trauma). All participating residents were given a diagram detailing the central location and seating arrangement. The outgoing attending was designated to handle

2013 Clinical Trials

1129. Validation of a Dynamic Evaluation Tool in Respiratory Failure

Evaluation Tool in Respiratory Failure (TELERESP) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT01807663 Recruitment Status : Terminated (Healthy volonteers study results show that the device is not enough reliable) First Posted : March 8, 2013 Last Update Posted : September 26, 2014 Sponsor: Centre (...) ] Healthy subjects will be recorded for one hour in seated positions 30 minutes and slept 30 min. Pneumotachograph recording will be realized during 5 minutes at the beginning and at the end of every phase of recording. The computer assuring the reception of the signals being remotely located to estimate of the transmission. All the patients will be registered in parallel with the VISURESP ® system (RBI Grenoble, France) and the measure of the transcutaneous PCO2 and SpO2(SenTec AG, Therwil, Switzerland

2013 Clinical Trials

1130. Sleep to Lower Elevated Blood Pressure

with a history of untreated OSA are eligible for inclusion). Known history of sleep disorders (i.e. narcolepsy; hypersomnias; parasomnias such as sleep walking, night terrors, recurring nightmares; periodic limb movements/restless leg syndrome; circadian rhythm sleep disorder) Unable to follow educational advice in the opinion of the clinician Baby or young children at home that wake during the night History of bipolar affective disorder History of psychosis History of major depression (defined as depression (...) Sleep to Lower Elevated Blood Pressure Sleep to Lower Elevated Blood Pressure - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Sleep to Lower Elevated Blood Pressure (SLEPT) The safety and scientific

2013 Clinical Trials

1131. Efficacy Study of Ambrisentan in Chinese Patients With Pulmonary Arterial Hypertension (PAH)

studies before adding more. Efficacy Study of Ambrisentan in Chinese Patients With Pulmonary Arterial Hypertension (PAH) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT01808313 Recruitment Status : Completed First Posted : March 11, 2013 Results First Posted : May 12, 2015 Last Update Posted : June 6 (...) Purpose: Treatment Official Title: An Open Label Phase IIIb Study to Evaluate Efficacy and Safety of Ambrisentan in Chinese Patients With Pulmonary Arterial Hypertension (PAH) Actual Study Start Date : December 1, 2012 Actual Primary Completion Date : August 15, 2014 Actual Study Completion Date : August 15, 2014 Resource links provided by the National Library of Medicine related topics: available for: resources: Arms and Interventions Go to Arm Intervention/treatment Experimental: ambrisentan

2013 Clinical Trials

1132. Motivational Support and Meal Preparation Training to Reduce Vascular Risk After Gestational Diabetes

remove one or more studies before adding more. Motivational Support and Meal Preparation Training to Reduce Vascular Risk After Gestational Diabetes (MoMM) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT01814995 Recruitment Status : Completed First Posted : March 20, 2013 Last Update Posted (...) activity levels. However, many women find it difficult to alter their lifestyle habits, especially if they have young children. In adults with type 2 diabetes, the investigators have been studying the effects of combining nutrition education with meal preparation training and pedometer-based self-monitoring to improve eating habits and increase activity levels. The investigators have shown that such a strategy can reduce hemoglobin A1C by 0.3% and correlates with small reductions in weight (Dasgupta et

2013 Clinical Trials

1133. Progressive Resistance Training of the Extensor Muscle of the Thigh in COPD-patients Hospitalized With an Exacerbation

number of saved studies (100). Please remove one or more studies before adding more. Progressive Resistance Training of the Extensor Muscle of the Thigh in COPD-patients Hospitalized With an Exacerbation The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT01812460 Recruitment Status : Withdrawn (The Study (...) and sit. STS: measures the number of times the patient can rise from a chair 43 cm to seat and sit during 30 seconds. The sit to stand test reflects the ability to deal with a very important part of every day life - to rise from a chair. 6 min walk: how far can the patient walk in 6 min. Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding

2013 Clinical Trials

1134. Chronic Remote Ischemic Conditioning to Modify Post-MI Remodeling

Conditioning to Modify Post-MI Remodeling (CRIC-RCT) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT01817114 Recruitment Status : Unknown Verified July 2016 by The Hospital for Sick Children. Recruitment status was: Recruiting First Posted : March 22, 2013 Last Update Posted : July 15, 2016 Sponsor (...) : The Hospital for Sick Children Collaborators: University Health Network, Toronto Sunnybrook Health Sciences Centre St. Michael's Hospital, Toronto Information provided by (Responsible Party): The Hospital for Sick Children Study Details Study Description Go to Brief Summary: During a heart attack, an artery carrying blood and oxygen to the heart becomes blocked, which causes damage to the heart muscle. When possible, a clot-busting drug is given or a procedure called angioplasty is performed soon after

2013 Clinical Trials

1135. Subthalamic Deep Brain Stimulation (DBS) in Parkinson's Disease

Stimulation (DBS) in Parkinson's Disease The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02012647 Recruitment Status : Completed First Posted : December 16, 2013 Last Update Posted : June 13, 2016 Sponsor: University of Florida Information provided by (Responsible Party): University of Florida Study (...) . The screening visit will occur up to 4 months before the first study visit, and can be scheduled to occur on the same day as the first study visit. This evaluation will include a review of medical history and clinical findings related to Parkinson's Disease (if applicable). There may be a neurological exam (physical exam). Women of child bearing potential will take a urine pregnancy test. If applicable, the medications currently used to treat Parkinson's Disease symptoms will be reviewed and subjects

2013 Clinical Trials

1136. Standard ACL Reconstruction vs ACL + Lateral Extra-Articular Tenodesis Study

. Standard ACL Reconstruction vs ACL + Lateral Extra-Articular Tenodesis Study (STAbiLiTY) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02018354 Recruitment Status : Active, not recruiting First Posted : December 23, 2013 Last Update Posted : September 26, 2017 Sponsor: University of Western Ontario (...) , 6, 12, 24 months ] For passive knee extension, the patient is seated with both legs extended on a table, heel propped so that the calf and upper thigh clear treatment table. The patient will be instructed to relax both quadriceps and hamstrings to assure passive measurement. For active-assisted knee flexion, the patient is seated with both legs extended on a table. They will be instructed to perform active-assisted knee flexion by placing one hand under their thigh to initiate flexion

2013 Clinical Trials

1137. Teen Video Study to Reduce Risky Driving and Sexual Behavior in Adolescents

Video Study to Reduce Risky Driving and Sexual Behavior in Adolescents (TVS) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02049710 Recruitment Status : Unknown Verified October 2015 by Carnegie Mellon University. Recruitment status was: Active, not recruiting First Posted : January 30, 2014 Last (...) Intervention/treatment Phase Pregnancy Sexually Transmitted Infections Automobile Accidents Behavioral: Seventeen Days Behavioral: Driving Skills for Life Not Applicable Detailed Description: Motor vehicle crashes cause one-third of teenage deaths and many serious injuries. Teen drivers ages 16 to 19 are four times more likely than older drivers to crash. Death and injuries could be reduced with a change in behaviors that include improved visual and attention skills while driving, more seat belt use

2013 Clinical Trials

1138. Evaluating the CG ASSIST Program for Caregiving Dyads

Dyads (CG ASSIST) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02021565 Recruitment Status : Completed First Posted : December 27, 2013 Results First Posted : March 1, 2018 Last Update Posted : March 1, 2018 Sponsor: VA Office of Research and Development Information provided by (Responsible Party (...) ) and their informal caregivers will result in improvements in caregiving processes (i.e., caregiving skills) and outcomes (i.e., safety during tasks) compared to the current standard of care and have beneficial direct and indirect effects for both members of the dyad. Secondary objectives are to determine the effects of the program on Veteran and caregiver subjective well-being (depression, quality of life) and to compare the relative effectiveness of two validated implementation modalities the traditional

2013 Clinical Trials

1139. Effects of Supplementation in Healthy Russian Population

Russian Population The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02224092 Recruitment Status : Completed First Posted : August 25, 2014 Last Update Posted : August 25, 2014 Sponsor: Access Business Group Collaborator: Russian Institute of Nutrition Information provided by (Responsible Party): Access (...) Business Group Study Details Study Description Go to Brief Summary: The objectives of this exploratory study are to (1) evaluate the effect of the multivitamin multimineral with phytonutrient product vs. placebo on heart health risk factors following twice-daily consumption for eight weeks; (2) To test the safety and tolerability of the multivitamin multimineral with phytonutrient product vs. placebo following twice-daily consumption for eight weeks. Condition or disease Intervention/treatment Phase

2013 Clinical Trials

1140. Staphylococcus Aureus Bacteremia Antibiotic Treatment Options

Antibiotic Treatment Options (SABATO) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT01792804 Recruitment Status : Recruiting First Posted : February 15, 2013 Last Update Posted : October 22, 2018 See Sponsor: Heinrich-Heine (...) , there is insufficient evidence that a full course of intravenous antibiotic therapy is always required in patients with a low risk of SAB-related complications. In a multicenter, open-label, randomized controlled trial we aim to demonstrate that an early switch from intravenous to oral antimicrobial therapy is non-inferior to a conventional 14-days course of intravenous therapy regarding efficacy and safety. An early switch from intravenous to oral therapy would provide several benefits such as earlier discharge

2013 Clinical Trials

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