How to Trip Rapid Review

Step 1: Select articles relevant to your search (remember the system is only optimised for single intervention studies)

Step 2: press

Step 3: review the result, and maybe amend the or if you know better! If we're unsure of the overall sentiment of the trial we will display the conclusion under the article title. We then require you to tell us what the correct sentiment is.

10,974 results for

E/M Examination Criteria

by
...
Latest & greatest
Alerts

Export results

Use check boxes to select individual results below

SmartSearch available

Trip's SmartSearch engine has discovered connected searches & results. Click to show

61. Narrative E-Writing Intervention (NeW-I) for Parents of Children With Chronic Life-Threatening Illness

of more than 3 months since time of study participation so as to ensure successfully completion of all intervention components before child's death. Able to speak, read and write in English, as well as to provide informed consent. Exclusion Criteria: Cannot provide informed consent Suffering from severely high levels of depressive symptoms, anxiety and psychological distress (i. e. score of 19 or higher on Patient Health Questionnaire-9 (PHQ-9) or score of 29 or higher on Kessler Psychological (...) Narrative E-Writing Intervention (NeW-I) for Parents of Children With Chronic Life-Threatening Illness Narrative E-Writing Intervention (NeW-I) for Parents of Children With Chronic Life-Threatening Illness - 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

2018 Clinical Trials

62. Study to Evaluate Constituents in Exhaled Breath and Room Air From Use of E-vapor Products and Conventional Cigarettes

Posted : July 30, 2018 Last Update Posted : December 5, 2018 Sponsor: Juul Labs, Inc. Collaborator: Inflamax Research Incorporated Information provided by (Responsible Party): Juul Labs, Inc. Study Details Study Description Go to Brief Summary: An open-label, single center, three-arm observational study to examine emissions from e-cigarettes versus conventional cigarettes under three environmental settings of typical residential, office and hospitality facilities. Condition or disease Intervention (...) Study to Evaluate Constituents in Exhaled Breath and Room Air From Use of E-vapor Products and Conventional Cigarettes Study to Evaluate Constituents in Exhaled Breath and Room Air From Use of E-vapor Products and Conventional Cigarettes - 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

2018 Clinical Trials

63. Evaluation of an E-intervention on MHBC for Chinese Cardiac Patients in Home-based Rehabilitation

(in m) and body weight (in kg) for calculating the BMI, using the equation "BMI=weight/ height square". Other Outcome Measures: Social-demographic information [ Time Frame: At the beginning of intervention (Baseline) ] The items consist of gender, age, marital status, education level, rehabilitation treatment history, and current work status. Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk (...) Evaluation of an E-intervention on MHBC for Chinese Cardiac Patients in Home-based Rehabilitation Evaluation of an E-intervention on MHBC for Chinese Cardiac Patients in Home-based Rehabilitation - 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

2018 Clinical Trials

64. E-Support Groups in Multiple Sclerosis

-hr weekly online journaling activities. Behavioral: e-Journaling placebo Online journaling activity. Other Name: e-Journaling Outcome Measures Go to Primary Outcome Measures : Percentage of enrolled participants who completed follow-up questionnaires [ Time Frame: 12 weeks ] Assess feasibility of the program: to retain and obtain completed questionnaires at immediate follow-up from 80% of enrolled participants (meeting the criteria of 75% attendance). Change in UCLA Loneliness Scale total score (...) E-Support Groups in Multiple Sclerosis E-Support Groups in Multiple Sclerosis - 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. E-Support Groups in Multiple Sclerosis (eSupport) The safety and scientific

2018 Clinical Trials

65. Criteria for appropriate use of FDG-PET in esophageal cancer

in the overall evidence for each outcome of interest. The GRADE approach for diagnostic recommendations was also used to elicit judgement from the panel members on benefit and harms trade-off for patient-important outcomes. The RAND method was used to vote and reach an agreement on the appropriateness criteria. Results: The panel examined and assessed the role of FDG-PET for the following 7 clinical indications: N staging of primary esophageal cancer; M staging of primary esophageal cancer; Target volume (...) . Criteria for appropriate use of FDG-PET in esophageal cancer. Bologna: Agenzia sanitaria e sociale regionale, Regione Emilia-Romagna (ASSR). ORIentamenti 4. 2011 Authors' conclusions Aim: The criteria reported in this document, are to be intended as guidance for programs of clinical governance aimed at: supporting clinicians on the use of FDG-PET; post hoc analyses of appropriate use of FDG-PET; contributing to the planning of the regional health service. Method: A panel of 26 experts, comprising

2011 Health Technology Assessment (HTA) Database.

66. Criteria for appropriate use of FDG-PET in colorectal cancer

in the overall evidence for each outcome of interest. The GRADE approach for diagnostic recommendations was also used to elicit judgement from the panel members on benefit and harms trade-off for patient-important outcomes. The RAND method was used to vote and reach an agreement on the appropriateness criteria. Results: The panel examined and assessed the role of FDG-PET for the following 7 clinical indications: N staging of primary esophageal cancer; M staging of primary esophageal cancer; Target volume (...) . Criteria for appropriate use of FDG-PET in colorectal cancer . Bologna: Agenzia sanitaria e sociale regionale, Regione Emilia-Romagna (ASSR). ORIentamenti 5. 2011 Authors' conclusions Aim: The criteria reported in this document, are to be intended as guidance for programs of clinical governance aimed at: supporting clinicians on the use of FDG-PET; post hoc analyses of appropriate use of FDG-PET; contributing to the planning of the regional health service. Method: A panel of 26 experts, comprising

2011 Health Technology Assessment (HTA) Database.

67. Criteria for appropriate use of FDG-PET in breast cancer

of confidence in the overall evidence for each outcome of interest. The GRADE approach for diagnostic recommendations was also used to elicit judgement from the panel members on benefit and harms trade-off for patient-important outcomes. The RAND method was used to vote and reach an agreement on the appropriateness criteria. Results: The panel examined and assessed the role of FDG-PET for the following 7 clinical indications: Diagnosis of primary breast cancer; N staging of primary breast cancer; M staging (...) , Longo G. Criteria for appropriate use of FDG-PET in breast cancer . Bologna: Agenzia sanitaria e sociale regionale, Regione Emilia-Romagna (ASSR). ORIentamenti 3. 2011 Authors' conclusions Aim: The criteria reported in this document, are to be intended as guidance for programs of clinical governance aimed at: supporting clinicians on the use of FDG-PET; post hoc analyses of appropriate use of FDG-PET; contributing to the planning of the regional health service. Method: A panel of 23 experts

2011 Health Technology Assessment (HTA) Database.

68. A Study to Examine the Safety, Tolerability and Biological Effects of REGN4461 in Healthy Volunteers

information, Layout table for eligibility information Ages Eligible for Study: 18 Years to 65 Years (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: Yes Criteria Key Inclusion Criteria Part A: Males and females 18 to 50 years of age, inclusive Body mass index (BMI) from 18.5 to <30.0 kg/m^2 Participant is judged by the investigator to be in good health and free from major comorbidities based on medical history, physical examination, laboratory safety tests performed (...) at screening and/or prior to administration of initial dose of study drug Part B: Males and females 18 to 65 years of age, inclusive Have a body mass index (BMI) from 25.0 to 40.0 kg/m^2 Participant is judged by the investigator to be free from major comorbidities based upon medical history, physical examination, laboratory safety tests performed at screening and/or prior to administration of initial dose of study drug. Subjects can have a history of mild hyperlipidemia and/or mild hypertension but should

2018 Clinical Trials

69. Examining the Effects of Juice Fasting

Accepts Healthy Volunteers: Yes Criteria Inclusion Criteria: Subjects considered as healthy by the investigator based on medical history and completion of the screening questionnaire. Subjects who, according to the investigator, can and will comply with the requirements of the protocol and are available for all scheduled visits at the investigational site. Healthy male or female aged between 18 and 35 (included) years 18.5 ≤BMI ≤ 30 kg/m² Ability to give their informed consent in writing Exclusion (...) Examining the Effects of Juice Fasting Examining the Effects of Juice Fasting - 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. Examining the Effects of Juice Fasting The safety and scientific validity

2018 Clinical Trials

70. ACCF/SCAI/AATS/AHA/ASE/ASNC/HFSA/HRS/SCCM/SCCT/SCMR/STS 2012 Appropriate Use Criteria for Diagnostic Catheterization

ACCF/SCAI/AATS/AHA/ASE/ASNC/HFSA/HRS/SCCM/SCCT/SCMR/STS 2012 Appropriate Use Criteria for Diagnostic Catheterization doi:10.1016/j.jacc.2012.03.003 published online May 9, 2012; J. Am. Coll. Cardiol. Kirtane, L. Samuel Wann, and R. Parker Ward Robert O. Bonow, Charles E. Chambers, Paul S. Chan, Gregory J. Dehmer, Ajay J. Resonance, Society of Thoracic Surgeons, Manesh R. Patel, Steven R. Bailey, Cardiovascular Computed Tomography, Society for Cardiovascular Magnetic of America, Heart Rhythm (...) 0735-1097/$36.00 Published by Elsevier Inc. doi:10.1016/j.jacc.2012.03.003 by on May 16, 2012 content.onlinejacc.org Downloaded from Appropriate Use Criteria Task Force Michael J. Wolk, MD, MACC, Chair Steven R. Bailey, MD, FACC, FSCAI, FAHA Pamela S. Douglas, MD, MACC, FAHA, FASE Robert C. Hendel, MD, FACC, FAHA, FASNC Christopher M. Kramer, MD, FACC, FAHA James K. Min, MD, FACC Manesh R. Patel, MD, FACC Leslee Shaw, PHD, FACC, FASNC Raymond F. Stainback, MD, FACC, FASE Joseph M. Allen, MA TABLE

2012 Society for Cardiovascular Angiography and Interventions

71. ACCF/SCAI/STS/AATS/AHA/ASNC/HFSA/SCCT 2012 Appropriate Use Criteria for Coronary Revascularization Focused Update

* Steven R. Bailey, MD, FACC, FSCAI§ Chirojit Mukherjee, MD†† John H. Calhoon, MD‡ Debabrata Mukherjee, MD, FACC* Blase A. Carabello, MD, FACC* Catherine M. Otto, MD, FACC* Milind Y. Desai, MBBS, FACC ¦¶ Carlos E. Ruiz, MD, PhD, FACC, FSCAI§ Fred H. Edwards, MD, FACC† Ralph L. Sacco, MD, MS, FAHA‡‡ Gary S. Francis, MD, FACC# Donnette Smith§§ Timothy J. Gardner, MD, FACC† James D. Thomas, MD, FACC ¦¦ ACCF Task Force Members Robert A. Harrington, MD, FACC, Chair Deepak L. Bhatt, MD, MPH, FACC, Vice Chair (...) ACCF/SCAI/STS/AATS/AHA/ASNC/HFSA/SCCT 2012 Appropriate Use Criteria for Coronary Revascularization Focused Update 1 © 2012 by the American College of Cardiology Foundation, the American Association for Thoracic Surgery, the Society for Cardiovascular Angiography and Interventions, and the Society of Thoracic Surgeons. 2012 ACCF/AATS/SCAI/STS Expert Consensus Document on Transcatheter Aortic Valve Replacement Developed in collaboration with the American Heart Association, American Society

2012 Society for Cardiovascular Angiography and Interventions

72. CCF/SCAI/STS/AATS/AHA/ASNC/HFSA/SCCT 2012 Appropriate Use Criteria for Coronary Revascularization Focused Update

College of Cardiology Vol. 59, No. 9, 2012 © 2012 by the American College of Cardiology Foundation ISSN 0735-1097/$36.00 Published by Elsevier Inc. doi:10.1016/j.jacc.2011.12.001 Downloaded From: http://content.onlinejacc.org/ on 09/09/2014Appropriate Use Criteria Task Force Michael J. Wolk, MD, MACC, Chair Steven R. Bailey, MD, FACC, FSCAI, FAHA Pamela S. Douglas, MD, MACC, FAHA Robert C. Hendel, MD, FACC, FAHA, FASNC Christopher M. Kramer, MD, FACC, FAHA James K. Min, MD, FACC Manesh R. Patel, MD (...) , FACC Leslee Shaw, PHD, FACC, FASNC Raymond F. Stainback, MD, FACC, FASE Joseph M. Allen, MA TABLE OF CONTENTS Abstract 858 Preface 859 Introduction 859 Methods 860 Indication Development 860 Scope of Indications 860 Technical Panel Selection 861 Rating Process and Scoring 861 General Assumptions 862 De?nitions 862 Abbreviations 863 Results of Updated Ratings 864 Table A. Focused Update: New or Revised Indications 864 Coronary Revascularization Appropriate Use Criteria (By Indication) 865 Table 1

2012 Society for Cardiovascular Angiography and Interventions

73. Vitamin E infused Polyethylene Liners, Regular Polyethylene Liners, Cross-Linked Polyethylene Liners for Knee Articular Surfacing in Adults : A Review of Clinical Effectiveness and Cost Effectiveness

Articular Resurfacing 2 oxidation. 7 It is believed vitamin E may reduce the rate of revision surgery (or failure). 7 In addition, there are claims vitamin E may improve tensile strength while preventing polyethylene degeneration by oxidation. 6 The purpose of the current review is to examine the comparative clinical effectiveness and cost- effectiveness of vitamin E infused polyethylene liners, cross-linked polyethylene liners and conventional polyethylene liners for knee articular resurfacing (...) between January 1, 2007 and October 25, 2012. Selection Criteria and Methods One reviewer screened the titles and abstracts of the retrieved publications and evaluated the full-text publications for final article selection (Table 1). Vitamin E Infused, Conventional, and Cross-Linked Polyethylene Liners for Knee Articular Resurfacing 3 Table 1: Selection Criteria Population Adults undergoing knee articular resurfacing Intervention THREE COMPARISONS 1. Vitamin E infused polyethylene liners versus cross

2012 Canadian Agency for Drugs and Technologies in Health - Rapid Review

74. Effects of Ecological Rythmic-acoustic Stimulation (E-RAS) on Motor Skills in Individuals With Parkinson's Disease

of the auditory cues; absence of significant cognitive impairment (i.e., Mini-Mental Status Examination (MMSE) > 24; Frontal Assessment Battery (FAB) > 13); absence of psychiatric or severe systemic illnesses; mild-to-moderate disability assessed by means of the modified Hoehn and Yahr (H&Y) staging scale (1,5 ≤ H&Y ≤ 3); no engagement in any rehabilitative program in the 3 months before the beginning of the study Exclusion Criteria: Contacts and Locations Go to Information from the National Library (...) Effects of Ecological Rythmic-acoustic Stimulation (E-RAS) on Motor Skills in Individuals With Parkinson's Disease Effects of Ecological Rythmic-acoustic Stimulation (E-RAS) on Motor Skills in Individuals With Parkinson's Disease - 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

2017 Clinical Trials

75. Effects of Vitamin E Supplementation on Free Radicals and Fat Level of Obese Adolescence in Jakarta, Indonesia

group receiving treatment of vitamin E and other group receiving placebo. The dose and duration of vitamin E treatment is 400 IU per day for 2 months. At the end of treatment, all subjects had to run the same medical interview, physical examination and blood test. Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 69 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: Quadruple (Participant, Care (...) /ml Secondary Outcome Measures : Total Cholesterol [ Time Frame: 8 weeks ] mg/dl LDL Cholesterol [ Time Frame: 8 weeks ] mg/dl HDL Cholesterol [ Time Frame: 8 weeks ] mg/dl Triglycerides [ Time Frame: 8 weeks ] mg/dl Body weight [ Time Frame: 8 weeks ] kilograms Body Height [ Time Frame: 8 weeks ] centimeters BMI [ Time Frame: 8 weeks ] kg/m^2 Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk

2017 Clinical Trials

76. The Application of the E-health Education on Shared Care Program for Patients With Type 2 Diabetes

. Recruitment status was: Recruiting First Posted : February 23, 2017 Last Update Posted : February 23, 2017 Sponsor: Li-Li Chen Information provided by (Responsible Party): Li-Li Chen, China Medical University Hospital Study Details Study Description Go to Brief Summary: This study will be a randomized controlled trial aimed at examining the effectiveness of the in e-health education on shared care program for patients with type 2 diabetes mellitus (T2DM). The experiment will be conducted over 1 year (...) will be measured at three time points including 1 month before the experiment, and 2 and 5 months after the experiment. The self-management conditions and quality of life of the subjects will be also recorded using relevant scales. Condition or disease Intervention/treatment Phase Type 2 Diabetes Mellitus Behavioral: E-health Education Other: Routine care Not Applicable Detailed Description: This study will be a randomized controlled trial aimed at examining the effectiveness of the in e-health education

2017 Clinical Trials

77. Barriers and opportunities to implementation of sustainable e-Health programmes in Uganda: A literature review (PubMed)

was undertaken between May and December 2015 and was complemented with hand searching and a document review of grey literature in the form of policy documents and reports obtained online or from the Ministry of Health's Resource Centre.The searches identified a total of 293 resources of which 48 articles met the inclusion criteria of being in English and describing e-Health implementation in Uganda. These were included in the study and were examined in detail.Uganda has trialled several e-Health and m-Health (...) Barriers and opportunities to implementation of sustainable e-Health programmes in Uganda: A literature review Most developing countries, including Uganda, have embraced the use of e-Health and m-Health applications as a means to improve primary healthcare delivery and public health for their populace. In Uganda, the growth in the information and communications technology industry has benefited the rural communities and also created opportunities for new innovations, and their application

Full Text available with Trip Pro

2017 African journal of primary health care & family medicine

78. Examining the Effects of an Improvisation Group

. Kendall, P.C., Robin, J.A., Hedtke, K.A., Suveg, C., Flannery-Schroeder, E. & Gosch, E. (2005). Considering CBT with Anxious Youth? Think Exposures. Cognitive and Behavioural Practice, 12, 136-150. Kindler, R.C. & Gray, A.A. (2010). Theater and Therapy: How Improvisation Informs the Analytic Hour. Psychoanalytic Inquiry, 30, 254-266. doi: 10.1080/07351690903206223 Sheesley, A.P., Pfeffer, M. & Barish, B. (2016). Comedic Improv Therapy for the Treatment of Social Anxiety Disorder. Journal of Creativity (...) Examining the Effects of an Improvisation Group Examining the Effects of an Improvisation Group - 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. Examining the Effects of an Improvisation Group The safety

2017 Clinical Trials

79. Examining the Effects of a Team-based Running Program

patients. South African Journal of Sports Medicine. 2013;25(2):55. doi: 10.7196/SAJSM.481. Quelhas Martins A, Kavussanu M, Willoughby A, Ring C. Moderate intensity exercise facilitates working memory. Psychology of Sport and Exercise. 2013;14(3):323-328. doi: 10.1016/j.psychsport.2012.11.010 Dal Grande E, Taylor A, Wilson D. South australian health and wellbeing survey, december 2000. Centre for Population Studies in Epidemiology. 2002. Rosenberg M. Society and the adolescent self-image. Princeton, NJ (...) Examining the Effects of a Team-based Running Program Examining the Effects of a Team-based Running Program - 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. Examining the Effects of a Team-based Running

2017 Clinical Trials

80. AIUM Practice Parameter for the Performance of a Thyroid and Parathyroid Ultrasound Examination

-quality ultrasound examinations. The parameters re?ect what the AIUM considers the minimum criteria for a complete examination in each area but are not intended to establish a legal standard of care. AIUM-accredited practices are expected to generally follow the parameters with recognition that deviations from these parameters will be needed in some cases, depending on patient needs and available equipment. Practices are encouraged to go beyond the parameters to provide additional ser- vice (...) ) Committee.JAmCollRadiol 2015; 12: 1272–1279. 11. Burke CJ, Thomas RH, Howlett D. Imaging the major salivary glands. Br J Oral Maxillofac Surg 2011; 49:261–269. 12. Lee YY, Wong KT, King AD, Ahuja AT. Imaging of salivary gland tumours. Eur J Radiol 2008; 66:419–436. 13. Cornec D, Jousse-Joulin S, Pers JO, et al. Contribution of salivary gland ultrasonography to the diagnosis of Sjogren’s syndrome: toward new diagnostic criteria? Arthritis Rheum 2013; 65:216–225. 14. Theander E, Mandl T. Primary Sjogren’s syndrome

2013 American Institute of Ultrasound in Medicine

To help you find the content you need quickly, you can filter your results via the categories on the right-hand side >>>>